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Human skin
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| Human skin | |
|---|---|
| Details | |
| System | Integumentary system |
| Identifiers | |
| Latin | cutis |
| TA98 | A16.0.00.002 |
| TA2 | 7041 |
| TH | H3.12.00.1.00001 |
| FMA | 7163 |
| Anatomical terminology | |
The human skin is the outer covering of the body and is the largest organ of the integumentary system. The skin has up to seven layers of ectodermal tissue guarding muscles, bones, ligaments and internal organs. Human skin is similar to most of the other mammals' skin, and it is very similar to pig skin. Though nearly all human skin is covered with hair follicles, it can appear hairless. There are two general types of skin: hairy and glabrous skin (hairless). The adjective cutaneous literally means "of the skin" (from Latin cutis, skin).
Skin plays an important immunity role in protecting the body against pathogens and excessive water loss. Its other functions are insulation, temperature regulation, sensation, synthesis of vitamin D, and the protection of vitamin B folates. Severely damaged skin will try to heal by forming scar tissue. This is often discoloured and depigmented.
In humans, skin pigmentation (affected by melanin) varies among populations, and skin type can range from dry to non-dry and from oily to non-oily. Such skin variety provides a rich and diverse habitat for the approximately one thousand species of bacteria from nineteen phyla which have been found on human skin.
Structure
[edit]
Human skin shares anatomical, physiological, biochemical and immunological properties with other mammalian lines. Pig skin especially shares similar epidermal and dermal thickness ratios to human skin: pig and human skin share similar hair follicle and blood vessel patterns; biochemically the dermal collagen and elastin content is similar in pig and human skin; and pig skin and human skin have similar physical responses to various growth factors.[1][2]
Skin has mesodermal cells which produce pigmentation, such as melanin provided by melanocytes, which absorb some of the potentially dangerous ultraviolet radiation (UV) in sunlight. It contains DNA repair enzymes that help reverse UV damage. People lacking the genes for these enzymes have high rates of skin cancer. One form predominantly produced by UV light, malignant melanoma, is particularly invasive, causing it to spread quickly, and can often be deadly. Human skin pigmentation varies substantially between populations; this has led to the classification of people(s) on the basis of skin colour.[3]
In terms of surface area, the skin is the second largest organ in the human body (the inside of the small intestine is 15 to 20 times larger). For the average adult human, the skin has a surface area of 1.5–2.0 square metres (15–20 sq ft). The thickness of the skin varies considerably over all parts of the body, and between men and women, and young and old. An example is the skin on the forearm, which is on average 1.3 mm in males and 1.26 mm in females.[4] One average square inch (6.5 cm2) of skin holds 650 sweat glands, 20 blood vessels, 60,000 melanocytes, and more than 1,000 nerve endings.[5][better source needed] The average human skin cell is about 30 μm in diameter, but there are variants. A skin cell usually ranges from 25 to 40 μm2, depending on a variety of factors.
Skin is composed of three primary layers: the epidermis, the dermis and the hypodermis.[4]
Epidermis
[edit]The epidermis, "epi" coming from the Greek language meaning "over" or "upon", is the outermost layer of the skin. It forms the waterproof, protective wrap over the body's surface, which also serves as a barrier to infection and is made up of stratified squamous epithelium with an underlying basal lamina.

The epidermis contains no blood vessels, and cells in the deepest layers are nourished almost exclusively by diffused oxygen from the surrounding air[6] and to a far lesser degree by blood capillaries extending to the outer layers of the dermis. The main type of cells that make up the epidermis are Merkel cells, keratinocytes, with melanocytes and Langerhans cells also present. The epidermis can be further subdivided into the following strata (beginning with the outermost layer): corneum, lucidum (only in palms of hands and bottoms of feet), granulosum, spinosum, and basale. Cells are formed through mitosis at the basale layer. The daughter cells (see cell division) move up the strata changing shape and composition as they die due to isolation from their blood source. The cytoplasm is released and the protein keratin is inserted. They eventually reach the corneum and slough off (desquamation). This process is called "keratinization". This keratinized layer of skin is responsible for keeping water in the body and keeping other harmful chemicals and pathogens out, making skin a natural barrier to infection.[7]
Sublayers
[edit]The epidermis is divided into the following 5 sublayers or strata:
- Stratum corneum
- Stratum lucidum
- Stratum granulosum
- Stratum spinosum
- Stratum basale (also called "stratum germinativum")
Blood capillaries are found beneath the epidermis and are linked to an arteriole and a venule. Arterial shunt vessels may bypass the network in ears, the nose and fingertips.
Genes and proteins expressed in the epidermis
[edit]About 70% of all human protein-coding genes are expressed in the skin.[8][9] Almost 500 genes have an elevated pattern of expression in the skin. There are fewer than 100 genes that are specific for the skin, and these are expressed in the epidermis.[10] An analysis of the corresponding proteins show that these are mainly expressed in keratinocytes and have functions related to squamous differentiation and cornification.
Dermis
[edit]The dermis is the layer of skin beneath the epidermis that consists of connective tissue and cushions the body from stress and strain. The dermis is tightly connected to the epidermis by a basement membrane. It also harbours many nerve endings that provide the sense of touch and heat. It contains the hair follicles, sweat glands, sebaceous glands, apocrine glands, lymphatic vessels and blood vessels. The blood vessels in the dermis provide nourishment and waste removal from its own cells as well as from the stratum basale of the epidermis.
The dermis is structurally divided into two areas: a superficial area adjacent to the epidermis, called the papillary region, and a deep thicker area known as the reticular region.
Papillary region
[edit]The papillary region is composed of loose areolar connective tissue. It is named for its finger-like projections called papillae, which extend toward the epidermis. The papillae provide the dermis with a "bumpy" surface that interdigitates with the epidermis, strengthening the connection between the two layers of skin.
In the palms, fingers, soles, and toes, the influence of the papillae projecting into the epidermis forms contours in the skin's surface. These epidermal ridges occur in patterns (see: fingerprint) that are genetically and epigenetically determined and are therefore unique to the individual, making it possible to use fingerprints or footprints as a means of identification.
Reticular region
[edit]The reticular region lies deep in the papillary region and is usually much thicker. It is composed of dense irregular connective tissue, and receives its name from the dense concentration of collagenous, elastic, and reticular fibres that weave throughout it. These protein fibres give the dermis its properties of strength, extensibility, and elasticity.
Also located within the reticular region are the roots of the hairs, sebaceous glands, sweat glands, receptors, nails, and blood vessels.
Tattoo ink is held in the dermis. Stretch marks, often from adolescent growth spurts, weight gain, pregnancy and obesity, are also located in the dermis.
Subcutaneous tissue
[edit]The subcutaneous tissue (also hypodermis and subcutis) is not part of the skin, but lies below the dermis of the cutis. Its purpose is to attach the skin to underlying bone and muscle as well as supplying it with blood vessels and nerves. It consists of loose connective tissue, adipose tissue and elastin. The main cell types are fibroblasts, macrophages and adipocytes (subcutaneous tissue contains 50% of body fat). Fat serves as padding and insulation for the body.
Cross-section
[edit]Cell count and cell mass
[edit]Skin cell table
[edit]The below table identifies the skin cell count and aggregate cell mass estimates for a 70 kg adult male (ICRP-23; ICRP-89, ICRP-110).[11][12][13]
Tissue mass is defined at 3.3 kg (ICRP-89, ICRP110) and addresses the skin's epidermis, dermis, hair follicles, and glands. The cell data is extracted from 'The Human Cell Count and Cell Size Distribution',[14][15] Tissue-Table tab in the Supporting Information SO1 Dataset (xlsx). The 1200 record Dataset is supported by extensive references for cell size, cell count, and aggregate cell mass.
Detailed data for below cell groups are further subdivided into all the cell types listed in the above sections and categorized by epidermal, dermal, hair follicle, and glandular subcategories in the dataset and on the dataset's graphical website interface.[16] While adipocytes in the hypodermal adipose tissue are treated separately in the ICRP tissue categories, fat content (minus cell-membrane-lipids) resident in the dermal layer (Table-105, ICRP-23) is addressed by the below interstitial-adipocytes in the dermal layer.
| Named tissue and associated cell groups |
Cell count | Aggregate cell mass (g) |
Percent of total mass |
|---|---|---|---|
| Skin total | 6.1E+11 | 846.7 | 100% |
| Adipocyte | 7.3E+08 | 291.9 | 34.5% |
| Endothelial cell (EnCs) | 1.5E+10 | 6.16 | 0.7% |
| Epithelial cells (EpC) | 4.1E+11 | 313.9 | 37.1% |
| Eccrine gland | 1.7E+11 | 105 | 12.4% |
| Epidermal keratinocytes | 1.1E+11 | 85.5 | 10.1% |
| Hair follicle | 1.3E+11 | 119.9 | 14.2% |
| Mechanoreceptors | 4.9E+09 | 3.6 | 0.4% |
| Epithelial cells (EpC); non-nucleated | 7.2E+10 | 28.2 | 3.3% |
| Fibroblasts | 4.3E+10 | 94.6 | 11.2% |
| Myocytes | 2.6E+07 | 0.08 | 0.01% |
| Neuroglia | 8.5E+09 | 12.8 | 1.5% |
| Perivascular cells / Pericytes / Mural | 1.5E+09 | 0.56 | 0.07% |
| Stem cells; epithelial (EpSC) | 3.6E+09 | 1.50 | 0.2% |
| White blood cells | 5.4E+10 | 97.1 | 11.5% |
| Granulocytes (mast cell) | 2.2E+10 | 32.6 | 3.8% |
| Lymphoid | 1.3E+10 | 1.6 | 0.2% |
| Monocyte-macrophage series | 1.9E+10 | 62.9 | 7.4% |
Development
[edit]Skin colour
[edit]Human skin shows high skin colour variety from the darkest brown to the lightest pinkish-white hues. Human skin shows higher variation in colour than any other single mammalian species and is the result of natural selection. Skin pigmentation in humans evolved to primarily regulate the amount of ultraviolet radiation (UVR) penetrating the skin, controlling its biochemical effects.[17]
The actual skin colour of different humans is affected by many substances, although the single most important substance determining human skin colour is the pigment melanin. Melanin is produced within the skin in cells called melanocytes and it is the main determinant of the skin colour of darker-skinned humans. The skin colour of people with light skin is determined mainly by the bluish-white connective tissue under the dermis and by the haemoglobin circulating in the veins of the dermis. The red colour underlying the skin becomes more visible, especially in the face, when, as consequence of physical exercise or the stimulation of the nervous system (anger, fear), arterioles dilate.[18]
There are at least five different pigments that determine the colour of the skin.[19][20] These pigments are present at different levels and places.
- Melanin: It is brown in colour and present in the basal layer of the epidermis.
- Melanoid: It resembles melanin but is present diffusely throughout the epidermis.
- Carotene: This pigment is yellow to orange in colour. It is present in the stratum corneum and fat cells of dermis and superficial fascia.
- Hemoglobin (also spelled haemoglobin): It is found in blood and is not a pigment of the skin but develops a purple colour.
- Oxyhemoglobin: It is also found in blood and is not a pigment of the skin. It develops a red colour.
There is a correlation between the geographic distribution of UV radiation (UVR) and the distribution of indigenous skin pigmentation around the world. Areas that highlight higher amounts of UVR reflect darker-skinned populations, generally located nearer towards the equator. Areas that are far from the tropics and closer to the poles have lower concentration of UVR, which is reflected in lighter-skinned populations.[21]
In the same population it has been observed that adult human females are considerably lighter in skin pigmentation than males. Females need more calcium during pregnancy and lactation, and vitamin D, which is synthesized from sunlight, helps in absorbing calcium. For this reason it is thought that females may have evolved to have lighter skin in order to help their bodies absorb more calcium.[22]
The Fitzpatrick scale[23][24] is a numerical classification schema for human skin colour developed in 1975 as a way to classify the typical response of different types of skin to ultraviolet (UV) light:
| I | Always burns, never tans | Pale, Fair, Freckles |
| II | Usually burns, sometimes tans | Fair |
| III | May burn, usually tans | Light Brown |
| IV | Rarely burns, always tans | Olive brown |
| V | Moderate constitutional pigmentation | Brown |
| VI | Marked constitutional pigmentation | Black |
Ageing
[edit]

As skin ages, it becomes thinner and more easily damaged. Intensifying this effect is the decreasing ability of skin to heal itself as a person ages.
Among other things, skin ageing is noted by a decrease in volume and elasticity. There are many internal and external causes to skin ageing. For example, ageing skin receives less blood flow and lower glandular activity.
A validated comprehensive grading scale has categorized the clinical findings of skin ageing as laxity (sagging), rhytids (wrinkles), and the various facets of photoageing, including erythema (redness), and telangiectasia, dyspigmentation (brown discolouration), solar elastosis (yellowing), keratoses (abnormal growths) and poor texture.[25]
Cortisol causes degradation of collagen,[26] accelerating skin ageing.[27]
Anti-ageing supplements are used to treat skin ageing.[citation needed]
Photoageing
[edit]Photoageing has two main concerns: an increased risk for skin cancer and the appearance of damaged skin. In younger skin, sun damage will heal faster since the cells in the epidermis have a faster turnover rate, while in the older population the skin becomes thinner and the epidermis turnover rate for cell repair is lower, which may result in the dermis layer being damaged.[28]
UV-induced DNA damage
[edit]UV-irradiation of human skin cells generates damages in DNA through direct photochemical reactions at adjacent thymine or cytosine residues on the same strand of DNA.[29] Cyclobutane pyrimidine dimers formed by two adjacent thymine bases, or by two adjacent cytosine bases, in DNA are the most frequent types of DNA damage induced by UV. Humans, as well as other organisms, are capable of repairing such UV-induced damages by the process of nucleotide excision repair.[29] In humans this repair process protects against skin cancer.[29]
Types
[edit]This section needs expansion. You can help by adding to it. (March 2022) |
Though most human skin is covered with hair follicles, some parts can be hairless. There are two general types of skin, hairy and glabrous skin (hairless).[30] The adjective cutaneous means "of the skin" (from Latin cutis, skin).[31]
Functions
[edit]Skin performs the following functions:
- Protection: an anatomical barrier from pathogens and damage between the internal and external environment in bodily defence; Langerhans cells in the skin are part of the adaptive immune system.[7][32] Perspiration contains lysozyme that break the bonds within the cell walls of bacteria.[33]
- Sensation: contains a variety of nerve endings that react to heat and cold, touch, pressure, vibration, and tissue injury; see somatosensory system and haptics.
- Heat regulation: the skin contains a blood supply far greater than its requirements, which allows precise control of energy loss by radiation, convection and conduction. Dilated blood vessels increase perfusion and heat loss, while constricted vessels greatly reduce cutaneous blood flow and conserve heat.
- Control of evaporation: the skin provides a relatively dry and semi-impermeable barrier to fluid loss.[32] Loss of this function contributes to the massive fluid loss in burns.
- Aesthetics and communication: others see skin and can assess mood, physical state and attractiveness.
- Storage and synthesis: acts as a storage centre for lipids and water, as well as a means of synthesis of vitamin D by action of UV on certain parts of the skin.
- Excretion: sweat contains urea, however its concentration is 1/130th that of urine, hence excretion by sweating is at most a secondary function to temperature regulation.
- Absorption: the cells comprising the outermost 0.25–0.40 mm of the skin are "almost exclusively supplied by external oxygen", although the "contribution to total respiration is negligible".[6] In addition, medicine can be administered through the skin, by ointments or by means of adhesive patch, such as the nicotine patch or iontophoresis. The skin is an important site of transport in many other organisms.
- Water resistance: The skin acts as a water-resistant barrier so essential nutrients are not washed out of the body.[32]
Skin flora
[edit]The human skin is a rich environment for microbes.[34][35] Around 1,000 species of bacteria from 19 bacterial phyla have been found.[35][34] Most come from only four phyla: Actinomycetota (51.8%), Bacillota (24.4%), Pseudomonadota (16.5%), and Bacteroidota (6.3%). Propionibacteria and Staphylococci species were the main species in sebaceous areas. There are three main ecological areas: moist, dry and sebaceous. In moist places on the body Corynebacteria together with Staphylococci dominate. In dry areas, there is a mixture of species but dominated by Betaproteobacteria and Flavobacteriales. Ecologically, sebaceous areas had greater species richness than moist and dry ones. The areas with least similarity between people in species were the spaces between fingers, the spaces between toes, axillae, and umbilical cord stump. Most similarly were beside the nostril, nares (inside the nostril), and on the back.
Reflecting upon the diversity of the human skin researchers on the human skin microbiome have observed: "hairy, moist underarms lie a short distance from smooth dry forearms, but these two niches are likely as ecologically dissimilar as rainforests are to deserts."[34]
The NIH conducted the Human Microbiome Project to characterize the human microbiota, which includes that on the skin and the role of this microbiome in health and disease.[36]
Microorganisms like Staphylococcus epidermidis colonize the skin surface. The density of skin flora depends on region of the skin. The disinfected skin surface gets recolonized from bacteria residing in the deeper areas of the hair follicle, gut and urogenital openings.
Clinical significance
[edit]Diseases of the skin include skin infections and skin neoplasms (including skin cancer). Dermatology is the branch of medicine that deals with conditions of the skin.[30]
There are seven cervical, twelve thoracic, five lumbar, and five sacral.[clarification needed] Certain diseases like shingles, caused by varicella-zoster infection, have pain sensations and eruptive rashes involving dermatomal distribution. Dermatomes are helpful in the diagnosis of vertebral spinal injury levels. Aside from the dermatomes, the epidermis cells are susceptible to neoplastic changes, resulting in various cancer types.[37]
The skin is also valuable for diagnosis of other conditions, since many medical signs show through the skin. Skin colour affects the visibility of these signs, a source of misdiagnosis in unaware medical personnel.[38][39][40]
Society and culture
[edit]Hygiene and skin care
[edit]The skin supports its own ecosystems of microorganisms, including yeasts and bacteria, which cannot be removed by any amount of cleaning. Estimates place the number of individual bacteria on the surface of human skin at 7.8 million per square centimetre (50 million per square inch), though this figure varies greatly over the average 1.9 square metres (20 sq ft) of human skin. Oily surfaces, such as the face, may contain over 78 million bacteria per square centimetre (500 million per square inch). Despite these vast quantities, all of the bacteria found on the skin's surface would fit into a volume the size of a pea.[41] In general, the microorganisms keep one another in check and are part of a healthy skin. When the balance is disturbed, there may be an overgrowth and infection, such as when antibiotics kill microbes, resulting in an overgrowth of yeast. The skin is continuous with the inner epithelial lining of the body at the orifices, each of which supports its own complement of microbes.
Cosmetics should be used carefully on the skin because these may cause allergic reactions. Each season requires suitable clothing in order to facilitate the evaporation of the sweat. Sunlight, water and air play an important role in keeping the skin healthy.
Oily skin
[edit]Oily skin is caused by over-active sebaceous glands, that produce a substance called sebum, a naturally healthy skin lubricant.[42][43] A high glycemic-index diet and dairy products (except for cheese) consumption increase IGF-1 generation, which in turn increases sebum production.[43] Overwashing the skin does not cause sebum overproduction but may cause dryness.[43]
When the skin produces excessive sebum, it becomes heavy and thick in texture, known as oily skin.[43] Oily skin is typified by shininess, blemishes and pimples.[42] The oily-skin type is not necessarily bad, since such skin is less prone to wrinkling, or other signs of ageing,[42] because the oil helps to keep needed moisture locked into the epidermis (outermost layer of skin). The negative aspect of the oily-skin type is that oily complexions are especially susceptible to clogged pores, blackheads, and buildup of dead skin cells on the surface of the skin.[42] Oily skin can be sallow and rough in texture and tends to have large, clearly visible pores everywhere, except around the eyes and neck.[42]
Permeability
[edit]Human skin has a low permeability; that is, most foreign substances are unable to penetrate and diffuse through the skin. Skin's outermost layer, the stratum corneum, is an effective barrier to most inorganic nanosized particles.[44][45] This protects the body from external particles such as toxins by not allowing them to come into contact with internal tissues. However, in some cases it is desirable to allow particles entry to the body through the skin. Potential medical applications of such particle transfer has prompted developments in nanomedicine and biology to increase skin permeability. One application of transcutaneous particle delivery could be to locate and treat cancer. Nanomedical researchers seek to target the epidermis and other layers of active cell division where nanoparticles can interact directly with cells that have lost their growth-control mechanisms (cancer cells). Such direct interaction could be used to more accurately diagnose properties of specific tumours or to treat them by delivering drugs with cellular specificity.
Nanoparticles
[edit]Nanoparticles 40 nm in diameter and smaller have been successful in penetrating the skin.[46][47][48] Research confirms that nanoparticles larger than 40 nm do not penetrate the skin past the stratum corneum.[46] Most particles that do penetrate will diffuse through skin cells, but some will travel down hair follicles and reach the dermis layer.
The permeability of skin relative to different shapes of nanoparticles has also been studied. Research has shown that spherical particles have a better ability to penetrate the skin compared to oblong (ellipsoidal) particles because spheres are symmetric in all three spatial dimensions.[48] One study compared the two shapes and recorded data that showed spherical particles located deep in the epidermis and dermis whereas ellipsoidal particles were mainly found in the stratum corneum and epidermal layers.[48] Nanorods are used in experiments because of their unique fluorescent properties but have shown mediocre penetration.
Nanoparticles of different materials have shown skin's permeability limitations. In many experiments, gold nanoparticles 40 nm in diameter or smaller are used and have shown to penetrate to the epidermis. Titanium oxide (TiO2), zinc oxide (ZnO), and silver nanoparticles are ineffective in penetrating the skin past the stratum corneum.[45][49] Cadmium selenide (CdSe) quantum dots have proven to penetrate very effectively when they have certain properties. Because CdSe is toxic to living organisms, the particle must be covered in a surface group. An experiment comparing the permeability of quantum dots coated in polyethylene glycol (PEG), PEG-amine, and carboxylic acid concluded the PEG and PEG-amine surface groups allowed for the greatest penetration of particles. The carboxylic acid coated particles did not penetrate past the stratum corneum.[48]
Increasing permeability
[edit]Scientists previously believed that the skin was an effective barrier to inorganic particles. Damage from mechanical stressors was believed to be the only way to increase its permeability.[50]
Recently, simpler and more effective methods for increasing skin permeability have been developed. Ultraviolet radiation (UVR) slightly damages the surface of skin and causes a time-dependent defect allowing easier penetration of nanoparticles.[51] The UVR's high energy causes a restructuring of cells, weakening the boundary between the stratum corneum and the epidermal layer.[51][50] The damage of the skin is typically measured by the transepidermal water loss (TEWL), though it may take 3–5 days for the TEWL to reach its peak value. When the TEWL reaches its highest value, the maximum density of nanoparticles is able to permeate the skin. While the effect of increased permeability after UVR exposure can lead to an increase in the number of particles that permeate the skin, the specific permeability of skin after UVR exposure relative to particles of different sizes and materials has not been determined.[51]
There are other methods to increase nanoparticle penetration by skin damage: tape stripping is the process in which tape is applied to skin then lifted to remove the top layer of skin; skin abrasion is done by shaving the top 5–10 μm off the surface of the skin; chemical enhancement applies chemicals such as polyvinylpyrrolidone (PVP), dimethyl sulfoxide (DMSO), and oleic acid to the surface of the skin to increase permeability;[52][53] electroporation increases skin permeability by the application of short pulses of electric fields. The pulses are high voltage and on the order of milliseconds when applied. Charged molecules penetrate the skin more frequently than neutral molecules after the skin has been exposed to electric field pulses. Results have shown molecules on the order of 100 μm to easily permeate electroporated skin.[53]
Applications
[edit]A large area of interest in nanomedicine is the transdermal patch because of the possibility of a painless application of therapeutic agents with very few side effects. Transdermal patches have been limited to administer a small number of drugs, such as nicotine, because of the limitations in permeability of the skin. Development of techniques that increase skin permeability has led to more drugs that can be applied via transdermal patches and more options for patients.[53]
Increasing the permeability of skin allows nanoparticles to penetrate and target cancer cells. Nanoparticles along with multi-modal imaging techniques have been used as a way to diagnose cancer non-invasively. Skin with high permeability allowed quantum dots with an antibody attached to the surface for active targeting to successfully penetrate and identify cancerous tumours in mice. Tumour targeting is beneficial because the particles can be excited using fluorescence microscopy and emit light energy and heat that will destroy cancer cells.[54]
Sunblock and sunscreen
[edit]Sunblock and sunscreen are different important skin-care products though both offer full protection from the sun.[55]
Sunblock—Sunblock is opaque and stronger than sunscreen, since it is able to block most of the UVA/UVB rays and radiation from the sun, and does not need to be reapplied several times in a day. Titanium dioxide and zinc oxide are two of the important ingredients in sunblock.[56]
Sunscreen—Sunscreen is more transparent once applied to the skin and also has the ability to protect against UVA/UVB rays, although the sunscreen's ingredients have the ability to break down at a faster rate once exposed to sunlight, and some of the radiation is able to penetrate to the skin. In order for sunscreen to be more effective it is necessary to consistently reapply and use one with a higher sun protection factor.
Diet
[edit]Vitamin A, also known as retinoids, benefits the skin by normalizing keratinization, downregulating sebum production, which contributes to acne, and reversing and treating photodamage, striae, and cellulite.
Vitamin D and analogues are used to downregulate the cutaneous immune system and epithelial proliferation while promoting differentiation.
Vitamin C is an antioxidant that regulates collagen synthesis, forms barrier lipids, regenerates vitamin E, and provides photoprotection.
Vitamin E is a membrane antioxidant that protects against oxidative damage and also provides protection against harmful UV rays. [57]
Several scientific studies confirmed that changes in baseline nutritional status affects skin condition. [58]
Mayo Clinic lists foods they state help the skin: fruits and vegetables, whole-grains, dark leafy greens, nuts, and seeds.[59]
See also
[edit]- Acid mantle
- Anthropodermic bibliopegy
- Artificial skin
- Callus – Thick area of skin
- Cutaneous structure development
- Fingerprint – Skin on fingertips
- Human body
- Hyperpigmentation – About excess skin colour
- Intertriginous
- List of cutaneous conditions
- Meissner's corpuscle
- Nude beaches
- Nude swimming
- Nudity
- Pacinian corpuscle
- Polyphenol antioxidant
- Skin cancer
- Skin lesion
- Skin repair
- Sunbathing
References
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pig skin has been shown to be the most similar to human skin. Pig skin is structurally similar to human epidermal thickness and dermal-epidermal thickness ratios. Pigs and humans have similar hair follicle and blood vessel patterns in the skin. Biochemically pigs contain dermal collagen and elastic content that is more similar to humans than other laboratory animals. Finally pigs have similar physical and molecular responses to various growth factors.
- ^ Liu J, Kim D, Brown L, Madsen T, Bouchard GF. "Comparison of Human, Porcine and Rodent Wound Healing With New Miniature Swine Study Data" (PDF). sinclairresearch.com. Sinclair Research Centre, Auxvasse, MO, USA; Veterinary Medical Diagnostic Laboratory, Columbia, MO, USA. Archived from the original (PDF) on 27 January 2018. Retrieved 27 January 2018.
Pig skin is anatomically, physiologically, biochemically and immunologically similar to human skin
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External links
[edit]- "Skin Conditions". MedlinePlus. U.S. National Library of Medicine. Retrieved 12 November 2013.
Human skin
View on GrokipediaAnatomical Structure
Epidermis
The epidermis is the outermost layer of the skin, consisting of stratified squamous keratinized epithelium that lacks blood vessels and relies on diffusion from the dermis for nutrients.[4] It primarily comprises keratinocytes, which undergo differentiation to form a protective barrier, along with melanocytes, Langerhans cells, and Merkel cells.[4] The epidermis varies in thickness across body regions, ranging from approximately 0.05 mm on the eyelids to 1.5 mm on the palms and soles, reflecting adaptations to mechanical stress and environmental exposure.[4][6] In thin skin, which covers most of the body, the epidermis features four layers: the stratum basale, stratum spinosum, stratum granulosum, and stratum corneum.[4] Thick skin, found on the palms and soles, includes an additional stratum lucidum between the granulosum and corneum.[4] The stratum basale, anchored to the basement membrane, contains stem cells that proliferate to renew the epidermis; above it, the stratum spinosum provides strength via desmosomes, while the stratum granulosum initiates keratinization with keratohyalin granules.[4] The stratum corneum consists of dead, flattened corneocytes filled with keratin, continuously sloughed off to maintain barrier integrity.[4] Keratinocytes constitute about 90% of epidermal cells and follow a lifecycle where basal keratinocytes divide asymmetrically, with daughter cells migrating upward, differentiating over 28 to 40 days, and eventually desquamating as the body sheds roughly 40,000 cells daily.[4][7] Melanocytes, located in the basal layer, produce melanin granules transferred to keratinocytes via dendrites, providing photoprotection; their density is approximately 1 per 10 basal cells in non-sun-exposed areas.[4] Langerhans cells, dendritic immune cells derived from bone marrow, comprise 2-4% of epidermal cells and function in antigen presentation, while Merkel cells, associated with nerve endings, contribute to tactile sensation.[4] This cellular composition and renewal process ensure the epidermis acts as a dynamic barrier against pathogens, UV radiation, and water loss.[4]Dermis
The dermis constitutes the middle layer of human skin, situated beneath the epidermis and overlying the hypodermis, and is primarily composed of dense irregular connective tissue rich in collagen and elastin fibers.[4] It accounts for roughly 90-95% of the total skin thickness, providing structural support, elasticity, and tensile strength to the integument.[7] The dermis harbors vascular networks, sensory nerve endings, lymphatic vessels, and adnexal structures such as hair follicles, sweat glands, and sebaceous glands, which anchor into its matrix.[3] Histologically, the dermis subdivides into two principal strata: the superficial papillary dermis and the deeper reticular dermis, which blend seamlessly without a distinct boundary.[4] The papillary dermis features loosely arranged type III collagen fibers, fine elastic fibers, and a higher density of fibroblasts, macrophages, and mast cells, forming dermal papillae that project upward to interdigitate with the overlying epidermis, enhancing nutrient exchange and mechanical adhesion.[8] In contrast, the reticular dermis contains thicker bundles of type I collagen fibers oriented in a coarse, interwoven network, interspersed with coarser elastin fibers, contributing to the skin's durability and recoil properties.[9] Dermal thickness exhibits regional variation, ranging from approximately 0.6 mm on the eyelids to 3-4 mm on the palms, soles, and dorsal aspects of the trunk, influenced by local mechanical demands and appendage density.[10] Fibroblasts within the dermis synthesize and maintain the extracellular matrix, including glycosaminoglycans that provide hydration and resilience.[11] Sensory structures such as Meissner's corpuscles predominate in the papillary layer, while Pacinian corpuscles reside deeper in the reticular layer, facilitating tactile discrimination and pressure sensation.[12]Hypodermis
The hypodermis, also termed the subcutaneous layer or superficial fascia, represents the deepest cutaneous layer situated beneath the dermis, primarily comprising adipose tissue interspersed with loose connective tissue. This layer anchors the integument to underlying muscles, bones, and organs, facilitating mobility while providing structural support.[3] It consists mainly of adipocytes for fat storage, alongside fibroblasts, macrophages, mast cells, and an extracellular matrix rich in collagen fibers, reticular fibers, and elastin, which contribute to its elasticity and resilience.[13] Blood vessels, lymphatics, and nerves traverse the hypodermis to supply the overlying dermis and epidermis, with larger-caliber vessels originating here.[4] Structurally, the hypodermis exhibits regional variations in organization; in areas such as the abdomen and buttocks, it forms distinct lobules of adipose tissue separated by fibrous septa, whereas in regions like the eyelids and genitalia, it is notably thin and less adipose-rich. Thickness ranges from approximately 0.1 mm in thin-skinned areas to over 30 mm in regions of high fat accumulation, influenced by factors including age, sex, body mass index, and anatomical site.[14] Aging typically leads to thinning of this layer, reducing its insulating capacity and increasing susceptibility to temperature dysregulation.[15] Key physiological roles of the hypodermis include thermoregulation through adipose insulation that minimizes heat loss, energy storage in the form of triglycerides within adipocytes for metabolic reserves, and mechanical shock absorption to protect deeper tissues from trauma.[16] It also aids in hormone production, such as leptin from adipocytes, influencing appetite and energy balance, and supports wound healing by providing a vascular scaffold.[17] Unlike the dermis, the hypodermis lacks epidermal appendages like hair follicles or sweat glands but permits their extension from superficial layers.[3]Skin Appendages
Skin appendages, also known as adnexal structures, are epidermal-derived components of the integumentary system that proliferate downward into the dermis, forming hair follicles, nails, sebaceous glands, and sweat glands; their development begins in the third fetal month from ectodermal downgrowths.[18] Hair follicles are distributed across the body, with approximately 100,000–150,000 on the head (including the scalp); the face has about 20,000 pores, primarily associated with hair follicles and sebaceous glands, and the remainder distributed across other body parts.[19][20] Hair follicles generate keratinized hair shafts consisting of an outer cuticle, central cortex, and optional medulla, with the follicle structured into an upper infundibulum, mid-isthmus, and lower segment enclosing the proliferative hair bulb and inductive dermal papilla.[18] The inner root sheath (with Henle, Huxley, and cuticle layers) and outer root sheath encase the growing hair, enabling cyclic phases of anagen growth, catagen regression, and telogen rest; associated arrector pili muscles and sensory innervation support piloerection for thermoregulation and tactile response.[18][21] Hair primarily protects against UV radiation and mechanical injury, aids in thermoregulation and sensory perception, and serves aesthetic and social signaling functions.[18] Nails form as rigid, translucent plates from the nail matrix's germinative cells, which produce compact, anuclear onychocytes rich in hard keratin but lacking a granular layer; the matrix underlies the proximal nail plate, with the lunula visible as its distal extent and the hyponychium sealing the free edge.[18][21] Nails protect underlying distal phalanges, enhance fine motor tasks like grasping and scratching, amplify tactile sensitivity, and contribute to manual dexterity.[18] Sebaceous glands comprise alveolar lobules of lipid-laden sebocytes that undergo holocrine disintegration to release sebum via short ducts emptying into hair follicles, with secretion regulated by androgens.[18][21] Sebum lubricates skin and hair shafts, forms a hydrophobic barrier against desiccation and pathogens, and exhibits antimicrobial properties through free fatty acids and other components.[18] Sweat glands subdivide into eccrine and apocrine variants, both coiled tubular structures but differing in distribution, activation, and output. Eccrine glands predominate body-wide (except lips and glans), with a secretory coil of clear and dark cells plus myoepithelial contractions in the deep dermis or hypodermis, connected by a straight duct traversing the epidermis to surface pores; they secrete watery, hypotonic fluid containing electrolytes and proteins via merocrine mechanism.[18][21] This sweat facilitates evaporative cooling for thermoregulation, minor excretion of waste, and antimicrobial defense.[18] Apocrine glands concentrate in axillae, groin, areolae, and perianal regions, featuring wider lumens lined by cuboidal epithelium and larger secretory coils in the dermis; dormant until puberty and hormonally responsive, they discharge viscous, protein-rich secretions (potentially odorous upon bacterial breakdown) into follicular canals via apocrine or partial holocrine modes.[18][21] Apocrine output may lubricate associated hair, support bacterial flora modulation, and convey pheromonal signals, though human roles remain less defined than in other mammals.[18]Cellular and Molecular Composition
Major Cell Types
Keratinocytes constitute approximately 90% of the cells in the epidermis and are the primary structural elements responsible for forming the skin's protective barrier through keratin production and desquamation. These cells originate from the basal layer, undergo differentiation as they migrate upward, and flatten into corneocytes in the stratum corneum, which are filled with keratin filaments cross-linked by disulfide bonds for mechanical strength.[22] Melanocytes, located in the basal layer of the epidermis at a ratio of about 1 per 10 keratinocytes, synthesize melanin within melanosomes and transfer these organelles via dendrites to adjacent keratinocytes, providing photoprotection against ultraviolet radiation and determining skin pigmentation through eumelanin and pheomelanin production.[22][4] Langerhans cells, dendritic immune cells comprising 2-4% of epidermal cells, originate from bone marrow precursors and reside primarily in the stratum spinosum; they express MHC class II molecules, capture antigens via pattern recognition receptors, and migrate to lymph nodes to initiate T-cell responses, serving as sentinels against pathogens.[4][22] Merkel cells, mechanosensory cells found in the basal epidermis often associated with hair follicles and touch domes, function as slowly adapting type I mechanoreceptors; they form synaptic complexes with sensory nerve endings and express neuroendocrine markers like cytokeratin 20, contributing to fine tactile discrimination.[4] In the dermis, fibroblasts are the predominant resident cells, synthesizing and remodeling extracellular matrix components such as type I and III collagen, elastin, and proteoglycans to maintain structural integrity and facilitate wound healing through cytokine secretion and matrix metalloproteinase activity.[23] Dermal immune cells, including macrophages (histiocytes) and mast cells, support innate immunity; macrophages phagocytose debris and present antigens, while mast cells release histamine and other mediators in response to IgE-mediated triggers, influencing vascular permeability and inflammation.[23] Endothelial cells line dermal blood vessels, regulating nutrient exchange and leukocyte trafficking via adhesion molecules like ICAM-1 and VCAM-1 during inflammatory responses.[24] In the hypodermis, adipocytes predominate, storing triglycerides for energy reserves and cushioning; these cells also secrete adipokines influencing metabolism and insulation, with white adipocytes being the primary type in adult human skin.[22]Extracellular Matrix and Proteins
The extracellular matrix (ECM) of human skin, primarily located in the dermis but also forming the basement membrane at the dermal-epidermal junction, consists of a network of fibrous proteins, glycoproteins, and proteoglycans that provide mechanical strength, elasticity, hydration, and signaling cues for cellular interactions. In the dermis, ECM components constitute approximately 90% of the tissue's dry weight, with collagens forming the dominant scaffold.[25] This matrix supports fibroblast activity, regulates tissue homeostasis, and facilitates wound repair, while its composition varies slightly across skin regions and with age.[26] Collagens are the most abundant proteins in dermal ECM, accounting for 70-80% of the dry weight, with type I collagen comprising the majority (approximately 80% of total collagen) to confer tensile strength and structural integrity through fibrillar assembly. Type III collagen, present at 10-15%, interweaves with type I fibrils to enhance flexibility and resilience, particularly in reticular fibers. Minor collagens, such as types V and VI, modulate fibril diameter and associate with cellular surfaces. In the basement membrane, type IV collagen forms a non-fibrillar network essential for anchoring the epidermis, self-assembling into sheets with isoforms including α1, α2, α5, and α6 chains.[26][25][27] Elastic fibers, composed of elastin (2-4% of dermal dry weight) cross-linked with microfibrils like fibrillin, enable skin recoil and viscoelasticity, preventing permanent deformation under mechanical stress. Glycoproteins such as fibronectin organize the matrix by binding integrins and collagens, promoting cell adhesion and migration during development and repair. Laminins, particularly laminin-511 in skin, polymerize in the basement membrane to initiate network assembly and support keratinocyte adhesion via integrin receptors.[26][26] Proteoglycans and associated glycosaminoglycans (GAGs) fill interstitial spaces, binding water to maintain hydration and regulate collagen fibrillogenesis. Decorin, the most abundant dermal proteoglycan with chondroitin/dermatan sulfate chains, binds type I collagen to control fibril spacing and modulates transforming growth factor-β signaling. Other key proteoglycans include versican (chondroitin sulfate, for viscoelasticity), biglycan (dermis and basement membrane, for growth factor sequestration), lumican (keratan sulfate, for fibril organization), and perlecan (heparan/chondroitin sulfate in basement membrane, linking laminin and collagen IV networks). Non-sulfated hyaluronan, a major GAG, interacts with proteoglycans to form hydrated gels, aiding epidermal-dermal separation and cell motility.[28][25][28]Genetic Expression Patterns
The human skin transcriptome encompasses expression of 14,224 proteins, representing 71% of the total human proteome, with 602 genes exhibiting elevated expression relative to other tissues.[29] Genome-wide transcriptomic profiling of skin biopsies has identified 417 genes with enriched expression in skin, including 106 genes upregulated at least five-fold compared to non-skin tissues, many of which encode proteins critical for barrier formation and structural integrity.[30] These patterns arise from the stratified architecture of skin, where gene expression differentiates sharply between the epidermis, dermis, and hypodermis to support specialized functions such as mechanical resilience and lipid storage.[31] In the epidermis, keratinocytes dominate gene expression, with high levels of keratin genes like KRT5 and KRT14 in the basal layer transitioning to KRT1 and KRT10 in suprabasal layers, facilitating cytoskeletal support and differentiation.[32] Barrier-related genes such as FLG (filaggrin), LOR (loricrin), and desmosomal components (DSG1, DSC1) peak in the stratum corneum, enabling cornification and waterproofing.[30] Single-cell RNA sequencing reveals four spatially distinct basal stem cell populations in the interfollicular epidermis, each with unique expression signatures involving proliferation markers (MKI67) and adhesion molecules.[32] Dermal fibroblasts display layer-specific heterogeneity, with papillary fibroblasts expressing genes like APCDD1, AXIN2, COLEC12, PTGDS, and COL18A1 for provisional matrix support, while reticular fibroblasts upregulate structural extracellular matrix components such as COL1A1, COL3A1, and ELN (elastin) for tensile strength.[33] Transcriptomic analyses confirm diurnal oscillations in both epidermal and dermal layers, with rhythms in clock genes (PER1, CLOCK) and metabolic pathways influencing up to 10% of expressed genes in healthy adults.[34] Hypodermal adipocytes contribute genes involved in lipid biosynthesis and insulation, such as FABP4 and PPARG, which modulate overlying dermal expression through paracrine signaling.[31] Cell-type-specific patterns further delineate skin function: melanocytes highly express melanin synthesis genes (MLANA, DCT, TYR), while Langerhans cells and resident T cells show immune surveillance markers like CD1A and CD69.[29] Recent single-cell atlases across anatomical sites highlight regional Hox gene gradients (HOXC13 in scalp, HOXD13 in distal limbs) driving site-specific expression, underscoring developmental origins of these patterns.[35] Such profiles, validated via immunohistochemistry and RNA sequencing, reveal minimal inter-subject variability in core patterns but sensitivity to aging and environmental factors.[30][33]Physiological Functions
Physical Barrier and Protection
The stratum corneum functions as the skin's principal physical barrier, comprising 15-20 layers of anucleate corneocytes filled with keratin filaments and surrounded by intercellular lipids including ceramides, cholesterol, and free fatty acids organized into lamellar sheets.[36] This structure, often described as a "bricks and mortar" model where corneocytes act as bricks and lipids as mortar, restricts transepidermal water loss to approximately 5-10 g/m²/h under normal conditions, preventing dehydration while blocking the ingress of hydrophilic and lipophilic xenobiotics, allergens, and microorganisms.[37] [38] Tight junctions in the stratum granulosum layer of the viable epidermis provide a complementary paracellular seal, composed of proteins such as claudins, occludins, and zonula occludens, which limit diffusion of ions, water, and solutes, thereby reinforcing the barrier against environmental insults.[39] Desmosomal attachments between corneocytes further enhance mechanical cohesion, distributing shear forces and resisting abrasion from physical trauma.[40] The barrier also confers protection against ultraviolet radiation through scattering and absorption by corneocyte keratin and, to a lesser extent, by melanin pigments transferred from melanocytes to keratinocytes, reducing penetration of UVB (280-320 nm) wavelengths that cause DNA damage.[41] The skin's surface acidity, maintained at pH 4.5-5.5 by dissociated fatty acids and other metabolites, creates an "acid mantle" that inhibits proliferation of pathogenic bacteria such as Staphylococcus aureus while favoring commensal flora.[42] In addition to passive physical exclusion, the barrier integrates active defenses; disruption of the stratum corneum, as occurs in conditions like atopic dermatitis, correlates with increased permeability and susceptibility to infections, underscoring its role in innate immunity.[43] Keratinocytes within the epidermis produce antimicrobial peptides, including cathelicidin LL-37 and human β-defensins, which are secreted into the intercellular space to lyse microbes that compromise the physical integrity.[44][39]Thermoregulation and Sensation
The skin maintains core body temperature through integrated mechanisms involving vascular control, sweat production, and insulation. During heat stress, cutaneous vasodilation mediated by sympathetic nerves increases skin blood flow up to 8 liters per minute, enabling radiative and convective heat loss equivalent to several times the resting metabolic rate.[45] Simultaneously, eccrine sweat glands, numbering approximately 2-4 million across the body surface, secrete hypotonic fluid at rates exceeding 2 liters per hour under maximal stimulation; its evaporation absorbs 2430 kJ per liter of heat from the skin.[46] In cold conditions, arteriolar vasoconstriction reduces peripheral blood flow by over 90%, conserving heat, while subcutaneous adipose tissue provides thermal insulation with conductivity as low as 0.2 W/m·K.[46] Basal insensible perspiration contributes 600-700 mL of water loss daily, supporting ongoing evaporative cooling even without overt sweating.[46] Skin sensation arises from specialized free nerve endings and encapsulated receptors distributed across epidermal and dermal layers, transducing environmental stimuli into neural signals via primary afferents. Mechanoreceptors predominate for tactile discrimination: Meissner corpuscles in dermal papillae detect transient light touch and low-frequency vibrations (2-50 Hz); Merkel cell-neurite complexes sustain fine spatial resolution for texture and pressure; Pacinian corpuscles sense deep pressure and high-frequency vibrations (>100 Hz); and Ruffini endings register skin stretch and sustained indentation.[47] Thermoreceptors, primarily unmyelinated C-fibers and thinly myelinated Aδ-fibers, include cold-sensitive spots peaking at 25°C and warm-sensitive at 40°C, with receptive fields spanning millimeters to centimeters.[48] Nociceptors, comprising polymodal C-fibers (responding to heat >43°C, cold <5°C, mechanical pinch, and irritants) and Aδ high-threshold mechanothermal fibers, initiate protective withdrawal reflexes and pain perception upon tissue-threatening stimuli.[49] Receptor density varies regionally—fingertips host over 100 mechanoreceptors per cm² versus <10 on the back—enabling adaptive sensitivity, with glabrous skin emphasizing precision touch and hairy skin integrating itch via pruriceptors.[47] These somatosensory inputs integrate in the spinal cord and thalamus, contributing to conscious perception and autonomic thermoregulatory adjustments.[46]Metabolic and Immune Roles
The human skin performs key metabolic functions, including the synthesis of vitamin D3, where ultraviolet B radiation (290–315 nm) converts 7-dehydrocholesterol in epidermal keratinocytes to previtamin D3, which thermally isomerizes to vitamin D3 (cholecalciferol) before release into circulation.[50] This process accounts for approximately 80–100% of endogenous vitamin D production in sun-exposed individuals, varying by factors such as skin pigmentation, latitude, and age, with darker skin requiring longer exposure due to higher melanin content absorbing UVB.[51] Skin also contributes to lipid metabolism by producing ceramides, cholesterol, and free fatty acids in keratinocytes via enzymes like elongases and desaturases, forming the stratum corneum's permeability barrier that prevents transepidermal water loss and supports antimicrobial defense.[52] Additionally, epidermal cells metabolize amino acids for protein synthesis in structural components such as keratin and filaggrin, with mitochondria in keratinocytes and fibroblasts driving ATP production essential for cellular maintenance and repair.[53][54] In immune roles, the skin acts as a frontline barrier through constitutive and inducible production of antimicrobial peptides (AMPs) by keratinocytes, including human β-defensins (hBD-1 to hBD-4) and cathelicidin (LL-37), which disrupt microbial membranes and recruit immune cells via chemokine activity.[55] These AMPs are upregulated in response to pathogens or injury through pathways like Toll-like receptors, providing rapid chemical defense independent of adaptive immunity.[56] Langerhans cells, dendritic cells comprising 3–5% of epidermal nucleated cells, serve as antigen-presenting sentinels, capturing antigens via dendrites extending through tight junctions and migrating to lymph nodes to initiate T-cell responses or promote tolerance in steady-state conditions.[57][58] Keratinocytes further coordinate immunity by secreting cytokines (e.g., IL-1, TNF-α) and expressing MHC class II molecules during inflammation, bridging innate and adaptive responses while dermal immune cells like mast cells and macrophages amplify clearance of invaders.[59] This integrated system maintains homeostasis, with disruptions linked to conditions like atopic dermatitis from reduced AMP expression.[55]Microbiome Interactions
The human skin microbiome comprises a diverse community dominated by bacteria from the phyla Actinobacteria (e.g., Cutibacterium acnes), Firmicutes (e.g., Staphylococcus epidermidis), and Proteobacteria (e.g., Corynebacterium spp.), with compositions varying by skin niche: sebaceous areas favor Cutibacterium, moist sites like the axilla favor Corynebacterium, and dry sites like the forearm exhibit higher diversity.[60] These commensals interact symbiotically with host cells, providing colonization resistance via resource competition, biofilm disruption, and antimicrobial production; for instance, S. epidermidis secretes serine protease Esp to dismantle S. aureus biofilms and bacteriocins like epidermin, pep5, and epilancin K7 to inhibit pathogens including MRSA.[61] Similarly, C. acnes produces propionic acid and cutimycin, suppressing S. aureus growth through short-chain fatty acid-mediated acidification and direct antimicrobial activity.[61] Microbe-host crosstalk modulates innate immunity, with commensals stimulating keratinocytes via Toll-like receptor 2 (TLR2) to upregulate antimicrobial peptides such as β-defensins and cathelicidins, enhancing barrier defense without excessive inflammation.[60] S. epidermidis lipoteichoic acid activates TLR2 to recruit and mature mast cells, while also dampening TLR3-driven proinflammatory responses post-injury, thereby preserving homeostasis.[62] These interactions extend to adaptive immunity, where early-life microbiota induce commensal-specific regulatory T cells via CD301+ dendritic cells for tolerance, and present microbial metabolites (e.g., glycolipids via CD1d or riboflavin via MR1) to foster innate-like T cells like NKT and MAIT cells.[62] In physiological contexts, such dynamics support wound healing by activating keratinocyte aryl hydrocarbon receptor (AhR) pathways for barrier repair and limit pathogen invasion; diverse communities reduce S. aureus colonization in mouse models by boosting innate defenses.[62][61] Host factors like sebum lipids and pH further stabilize these equilibria, with S. epidermidis phenol-soluble modulins selectively targeting pathogens while sparing host tissues.[60] Disruptions, though beyond core homeostasis, underscore the microbiome's role in sustaining immune vigilance and epidermal integrity.[60]Developmental Biology
Embryonic Formation
The embryonic formation of human skin originates from the ectoderm and mesoderm germ layers established during gastrulation in the third week of development. The epidermis derives from the surface ectoderm, while the dermis arises from mesenchymal cells of the mesoderm, including contributions from the lateral plate mesoderm and somitic dermatomes.[63][64] The hypodermis, or subcutaneous layer, forms later from mesodermal mesenchyme, providing insulation and fat storage as the embryo matures.[4] By the end of the fourth week, the surface ectoderm separates from the neural tube, forming a single-layered epithelium that constitutes the primitive epidermis.[63] This layer initially consists of cuboidal cells expressing keratins K5 and K14, marking commitment to epidermal lineage.[65] Mesenchymal cells migrate beneath the ectoderm around the same period, condensing to form the early dermis and initiating production of extracellular matrix components such as collagen types I and III.[66] Stratification of the epidermis begins around the eighth week, with the formation of a transient periderm layer overlying the basal keratinocytes to protect against amniotic fluid.[63] Intermediate layers emerge by the tenth to twelfth weeks, driven by signals like BMP and Wnt pathways that promote progenitor proliferation and differentiation into spinous and granular layers.[65] Concurrently, the dermis develops papillary and reticular subdivisions by the third month, with fibroblasts synthesizing fibronectin and laminin to anchor the epidermis via a basement membrane.[67] Appendage primordia, such as hair follicles and glands, initiate from epidermal placodes interacting with dermal condensates starting in the ninth week, regulated by epithelial-mesenchymal signaling involving FGF and Shh pathways.[65] By the end of the first trimester, the skin achieves a multilayered structure resembling the adult form, though cornification and barrier function mature postnatally.[64] These processes ensure the skin's role as a protective interface from early organogenesis.[68]Postnatal Maturation
The human skin at birth transitions from an aqueous intrauterine environment to air exposure, initiating rapid postnatal adaptations primarily in barrier function and hydration. In term infants, the stratum corneum consists of 10-15 cell layers, providing a competent initial barrier coated by vernix caseosa, which sheds within hours to days post-delivery, exposing the skin to environmental stressors and prompting keratinocyte differentiation.[69] Preterm infants born before 34 weeks gestation exhibit immature epidermis with only 2-3 stratum corneum layers, resulting in elevated transepidermal water loss (TEWL) rates—often exceeding 50 g/m²/h compared to adult levels of 5-10 g/m²/h—and heightened vulnerability to dehydration and infection.[69] [70] Postnatally, TEWL in preterm neonates decreases exponentially, approximating term infant levels within 2-3 weeks through accelerated corneocyte extrusion and lipid matrix compaction.[69] Dermal maturation involves reorganization of the extracellular matrix, with preterm neonates displaying edematous papillary dermis, sparse and immature collagen fibrils (diameter ~40 nm versus ~100 nm in adults), and underdeveloped anchoring fibrils at the dermo-epidermal junction.[69] Over the first months, collagen deposition increases, fibril diameter enlarges, and elastic fibers elongate, enhancing tensile strength and elasticity; by 6-12 months, dermal thickness approaches adult proportions in term infants.[69] Epidermal thickness, initially 30-50% thinner in infants than adults, thickens progressively via keratinocyte proliferation, reaching adult-like values (~100 μm) by approximately 6 years.[71] Skin surface pH, alkaline at birth (6.34-7.5) due to amniotic fluid residues, acidifies within the first postnatal week to 5.5-6.0 in term infants, driven by free fatty acids from vernix hydrolysis and microbial colonization, establishing the antimicrobial acid mantle.[69] This shift lags in preterm skin, correlating with delayed barrier integrity. Sebaceous gland activity peaks neonatally from maternal androgen influence, yielding sebum levels up to 10-fold higher than in older children, before regressing sharply by 6 months and remaining low until puberty.[69] Eccrine sweat glands, structurally present from mid-gestation, function immaturely at birth; thermoregulatory sweating emerges by 2 weeks in term infants, while full emotional and gustatory responses develop over the first 1-2 years.[69] Stratum corneum properties refine beyond infancy: corneocyte size, smaller in neonates (~600 μm² versus ~1000 μm² in adults), enlarges by age 6 years, coinciding with reduced TEWL and increased lipid compactness for sustained barrier efficacy.[71] Hydration levels transiently exceed adult norms between 3-12 months due to elevated natural moisturizing factors, then stabilize.[69] By 6-10 years, most structural and functional metrics—epidermal renewal rate, dermal vascular density, and sebum composition—align with adult skin, though microbiome integration and immune effector density continue evolving into adolescence.[71] These changes underpin reduced permeability and enhanced resilience, with deviations in preterm cohorts often mitigated by environmental humidity and emollient support.[72]Pigmentation Development
Melanocytes, the pigment-producing cells responsible for skin coloration, originate from neural crest-derived melanoblasts during early embryogenesis. Neural crest cells form around the third week of gestation, with melanoblast specification occurring progressively as pluripotent precursors commit to the melanogenic lineage under the influence of transcription factors such as MITF (microphthalmia-associated transcription factor).[73] [74] These melanoblasts migrate dorsolaterally through the developing embryo, reaching the epidermal basal layer by approximately 8 to 10 weeks of gestation in humans, where they differentiate into mature melanocytes.[75] This migration is guided by signaling pathways including KIT ligand and endothelin-3, ensuring proper distribution to the epidermis, hair follicles, and other sites.[76] Upon reaching the skin, melanocytes begin synthesizing melanin within melanosomes, organelles that mature through four stages: formation, enzymatic activation of tyrosinase, melanin deposition, and transfer to keratinocytes.[77] Eumelanin (brown-black) and pheomelanin (red-yellow) production ratios determine baseline pigmentation, with genetic variants in genes like MC1R influencing the balance from fetal stages.[78] By the second trimester, functional melanocytes are evident in fetal skin, though melanin content remains low until postnatal activation.[79] Premature infants exhibit even lighter pigmentation due to incomplete maturation, highlighting the role of gestational age in establishing initial melanin levels.[80] Postnatally, skin pigmentation undergoes maturation as constitutive melanin production increases, typically reaching adult levels by 2 to 3 years of age, with infants born relatively hypopigmented compared to their genetic potential.[81] This development involves enhanced melanocyte proliferation, melanosome transfer efficiency, and responsiveness to ultraviolet radiation, which stimulates tyrosinase activity via p53-mediated pathways.[82] Hormonal factors, such as androgens during puberty, further modulate pigmentation density, while evolutionary adaptations link darker baseline tones to higher UV exposure histories through selection on genes like SLC24A5.[83] Disruptions in this process, as seen in conditions like piebaldism from KIT mutations, underscore the sequential dependence on embryonic migration and postnatal regulation for uniform pigmentation.Biological Variations
Sex-Based Differences
Male skin is generally thicker than female skin, with the epidermis and dermis exhibiting greater dimensions in males due to higher collagen density and dermal extracellular matrix content.[84] This thickness difference, averaging 20-25% greater in men, persists across body sites and correlates with androgen influence, as testosterone promotes epidermal proliferation and fibroblast activity in the dermis.[85] [86] Female skin, influenced by estrogen, maintains relatively thinner strata but shows accelerated thinning post-menopause due to estrogen decline, which reduces collagen synthesis by up to 30% within five years.[87] Sebaceous gland activity differs markedly, with males producing higher sebum levels—often 2-3 times that of females—driven by dihydrotestosterone stimulating lipid secretion, leading to oilier skin and larger pores.[84] [85] Sweat glands also exhibit sexual dimorphism; males have higher sweat rates and eccrine gland density, facilitating greater thermoregulatory efficiency, while apocrine glands in areas like axillae are more active in males under hormonal stimulation.[85] Surface pH is lower in males (more acidic, around 4.5-5.0) compared to females (5.5-6.0), potentially influencing microbial colonization and barrier integrity.[84] Hair follicle distribution and growth cycles vary, with males displaying denser terminal hair on the face, chest, and back due to androgen sensitivity, whereas females predominate in scalp hair density but experience earlier androgenetic alopecia influenced by relative estrogen protection.[85] Pigmentation levels are higher in males, manifesting as darker constitutive skin color across populations, attributed to greater melanin production in melanocytes under sex hormone modulation, though this dimorphism is more pronounced in medium-pigmented groups than extremes.[84] [88] These differences extend to aging trajectories: male skin retains collagen longer but develops deeper wrinkles from repeated UV exposure and muscle activity, while female skin undergoes rapid post-menopausal atrophy, with estrogen loss impairing hyaluronic acid and elastin maintenance, resulting in finer but more numerous wrinkles.[89] [87] Hormonal axes underpin these traits; androgens sustain dermal robustness in males, whereas cyclic estrogen fluctuations in females support hydration and elasticity until menopause, after which interventions like selective estrogen receptor modulators may mitigate declines.[90] [91]Racial and Ethnic Variations
Human skin exhibits variations in pigmentation, structure, and appendage density attributable to genetic ancestry and evolutionary adaptations to environmental pressures such as ultraviolet radiation exposure. Populations with ancestry from equatorial regions, such as sub-Saharan Africans, typically possess higher epidermal melanin content, primarily eumelanin, which provides enhanced protection against UV-induced DNA damage.[92] In contrast, individuals of European descent often have lower melanin levels and a higher proportion of pheomelanin, facilitating greater vitamin D synthesis in low-UV environments.[93] These pigmentation differences correlate with melanosome size and distribution: larger, more dispersed melanosomes in darker skin enhance photoprotection, while smaller, clustered melanosomes predominate in lighter skin.[94] Structural variations in the epidermis include differences in stratum corneum layering and barrier function. Black skin generally features a greater number of corneocyte layers (up to 20-25 compared to 15-20 in White skin), contributing to a more compact barrier despite higher transepidermal water loss (TEWL), with studies reporting TEWL rates 20-30% elevated in Black versus White skin under basal conditions.[95] [96] Asian skin, meanwhile, shows reduced barrier strength and lower ceramide levels in the intercellular lipids, potentially increasing permeability to irritants.[97] Dermal thickness varies minimally across groups in youth, but Black skin often displays denser collagen bundles and more active fibroblasts, leading to slower photoaging manifestations compared to White skin.[98] Appendageal differences further distinguish ethnic skin types. Eccrine sweat gland density is higher in Caucasian populations (approximately 100-200 glands/cm² on the trunk) than in Black or East Asian groups (50-150 glands/cm²), influencing thermoregulatory efficiency and basal perspiration rates.[99] Hair follicle morphology varies markedly: Asian follicles are typically round, yielding straight, thick shafts with low density (about 80-120 follicles/cm² on the scalp); African follicles are elliptical or flat, producing tightly coiled, finer fibers at similar densities; Caucasian follicles exhibit intermediate shapes, resulting in wavy or straight hair with higher ellipticity variability.[100] [101] These traits reflect genetic polymorphisms in genes like EDAR (prevalent in East Asians) and KRT (keratin) families, shaping follicle curvature and sebum production.[102]| Ethnic Group | Stratum Corneum Layers (approx.) | TEWL (relative to White skin) | Sweat Gland Density (trunk, glands/cm²) | Scalp Hair Follicle Shape |
|---|---|---|---|---|
| Black | 20-25 | Higher (1.2-1.3x) | 50-150 | Elliptical/flat (coiled) |
| White | 15-20 | Baseline | 100-200 | Variable (wavy/straight) |
| East Asian | 15-20 | Similar or slightly lower | 50-150 | Round (straight) |
Age-Related Changes
As humans age, the skin undergoes progressive structural and functional alterations primarily driven by intrinsic factors such as reduced cellular proliferation and extracellular matrix degradation, compounded by extrinsic influences like cumulative UV exposure. These changes manifest as epidermal thinning, dermal atrophy, loss of elasticity, and impaired barrier function, contributing to increased susceptibility to injury and slower wound healing. Histological studies reveal that chronologically aged skin exhibits a 10-20% reduction in epidermal thickness by the seventh decade, with flattening of the dermo-epidermal junction reducing surface area for nutrient exchange by up to 40%.[104][105][106] In the epidermis, keratinocyte turnover slows due to diminished mitotic activity in the basal layer, leading to a thinner stratum corneum and compromised barrier integrity despite unchanged cell layer counts. Melanocyte density decreases by approximately 10-20% per decade after age 30, though surviving cells enlarge and form irregular clusters, resulting in lentigines (age spots) on sun-exposed areas; senescent melanocytes further exacerbate aging by secreting paracrine factors that impair keratinocyte function and promote inflammation.[104][107][108] The dermis experiences the most pronounced atrophy, with collagen content declining by about 1% annually after age 20—cumulatively up to 30% by age 60—due to reduced fibroblast synthesis and increased matrix metalloproteinase activity. Elastin fibers fragment and accumulate as abnormal elastotic material, diminishing tensile strength and causing fine wrinkles and sagging; fibroblast senescence accumulates with age, reducing extracellular matrix production and contributing to chronic low-grade inflammation via the senescence-associated secretory phenotype. Vascular networks thin and become tortuous, impairing perfusion and nutrient delivery.[109][110][111] Subcutaneous fat in the hypodermis diminishes, particularly on the face and hands, leading to contour changes and increased fragility; eccrine and sebaceous gland function declines, reducing sweat production by 50% or more and sebum secretion, which manifests as xerosis (dryness) and roughness. These alterations collectively heighten risks of bruising, tearing, and infection, with healing rates slowing due to impaired angiogenesis and fibroblast recruitment.[104][112][113]Permeability and Environmental Interactions
Molecular Permeability Mechanisms
The stratum corneum, the outermost layer of the epidermis, serves as the primary permeability barrier of human skin, consisting of flattened corneocytes embedded in a multilamellar lipid matrix composed mainly of ceramides, cholesterol, and free fatty acids arranged in orthogonal arrays that mimic a lipid bilayer.[114] This structure restricts the passive diffusion of most molecules, with permeability governed primarily by the intercellular lipid domains rather than the corneocytes themselves.[115] Molecular permeation occurs via three main pathways: intercellular, transcellular, and transappendageal. The intercellular route, predominant for lipophilic compounds, involves diffusion through the tortuous lipid bilayers between corneocytes, facilitated by partitioning into the non-polar lipid environment.[116] Transcellular permeation, less efficient due to the hydrophilic keratin-filled corneocytes, requires molecules to cross both lipid and aqueous phases sequentially, suiting polar or charged substances but hindered by energy barriers.[117] The transappendageal pathway traverses appendages such as hair follicles, sebaceous glands, and sweat ducts, accounting for approximately 0.1% of skin surface area but enabling entry of larger hydrophilic or ionized molecules that poorly penetrate the stratum corneum.[118] Key physicochemical factors influencing permeability include molecular size, lipophilicity, and ionization state. Molecules with molecular weights below 500 Da exhibit higher flux, as larger sizes increase diffusional resistance through the compact stratum corneum lattice.[119] Optimal lipophilicity, often measured by log P values between 1 and 3, balances partitioning into lipids and subsequent release into the underlying aqueous viable epidermis, with excessively hydrophilic (log P < 0) or hydrophobic (log P > 4) compounds showing reduced absorption.[120] Ionized forms predominate at physiological pH for weak acids or bases, further limiting permeation unless via appendageal routes, while non-ionized lipophilic neutrals permeate most readily through intercellular lipids.[121] These mechanisms underscore the skin's selective barrier function, evolved to prevent dehydration and xenobiotic entry while allowing limited transepidermal water loss of about 5-10 g/m²/h under normal conditions.[37]UV Protection and Damage
Human skin protects against ultraviolet (UV) radiation through multiple mechanisms in the epidermis, primarily the absorption and dissipation of UV photons by chromophores such as melanin, DNA, and proteins, converting harmful energy into heat without chemical alteration.[82] Melanin, synthesized by melanocytes in the basal layer, serves as the principal photoprotectant; eumelanin granules absorb UVB (280-315 nm) and UVA (315-400 nm) rays, reducing penetration by up to 50-85% depending on concentration, and scavenge free radicals generated by UV exposure.[122] [78] The stratum corneum further contributes by scattering shorter UVB wavelengths, while post-exposure responses like epidermal hyperplasia increase the skin's optical density, limiting subsequent UV transmission.[82] UV radiation nonetheless inflicts direct and indirect damage, with UVB primarily absorbed in the epidermis—penetrating only 10-20% of its energy beyond the stratum corneum—inducing DNA lesions such as cyclobutane pyrimidine dimers (CPDs) and 6-4 photoproducts, which distort DNA helices and, if unrepaired, cause signature C>T mutations at dipyrimidine sites.[123] [124] UVA, comprising 95% of solar UV reaching Earth, penetrates deeper (up to 1 mm into the dermis), generating reactive oxygen species (ROS) via photosensitization of endogenous molecules, leading to oxidative base damage, lipid peroxidation, and degradation of extracellular matrix components like collagen and elastin.[125] [126] Acute UV overexposure triggers erythema (sunburn) within 4-6 hours via prostaglandin-mediated inflammation, peaking at 24-48 hours, while chronic exposure accelerates intrinsic aging through matrix metalloproteinase activation and telomere shortening in fibroblasts.[127] [128] These processes elevate carcinogenesis risk; UV-induced immunosuppression via cytokine release and antigen-presenting cell depletion further impairs tumor surveillance, contributing to non-melanoma skin cancers (basal and squamous cell) and melanoma, with global incidence rates exceeding 1.5 million cases annually as of 2020 data.[129] [130] Susceptibility varies by skin phototype per the Fitzpatrick scale (I-VI), where types I-II (low melanin, fair skin) exhibit minimal tanning and high burning propensity after 10-20 minutes of unprotected midday sun exposure, correlating with 2-3 fold higher melanoma risk versus types V-VI; however, darker phototypes remain vulnerable to UVA-driven damage despite lower acute erythema.[131] [132] Melanin content inversely predicts DNA damage post-UV dose; for instance, after 1 minimal erythema dose (MED), fair skin shows 10-fold more CPDs than darkly pigmented skin.[133] Tanning, a delayed response peaking 7-10 days post-exposure, redistributes preexisting melanin and upregulates synthesis via p53-mediated tyrosinase activation, conferring modest protection equivalent to SPF 2-4.[134] [127]Absorption of Substances
The stratum corneum, the outermost layer of the epidermis, acts as the principal barrier to percutaneous absorption of substances, consisting of flattened corneocytes embedded in a lipid matrix that restricts diffusion of hydrophilic and large molecules.[40] This barrier function is attributed to the orthogonal arrangement of keratin filaments within corneocytes and the intercellular lipids, including ceramides, cholesterol, and free fatty acids, which form a tortuous path for penetrants.[38] Intact human skin exhibits low permeability, with absorption rates typically below 10% for most topically applied drugs over 24 hours, though this varies by substance properties.[135] Substances cross the skin primarily through passive diffusion following Fick's laws, governed by concentration gradients and partition coefficients between the vehicle and skin lipids.[136] The main route is intercellular, via lipid bilayers, while transcellular penetration through corneocytes is limited due to their hydrophilic keratin content, and transappendageal pathways through hair follicles and sweat glands account for less than 0.1% of total absorption in normal skin.[137] Lipophilic compounds with molecular weights under 500 Da and octanol-water partition coefficients (log P) around 1-3 penetrate most efficiently, as seen in transdermal delivery of nicotine (MW 162 Da, log P 1.2) achieving steady-state plasma levels via patches.[138] Skin condition profoundly influences absorption; compromised barriers from abrasion, hydration, or solvents like dimethyl sulfoxide increase permeability by disrupting lipid organization, potentially elevating uptake by orders of magnitude.[139] [140] Hydration swells corneocytes, widening intercellular spaces, while occlusion enhances it by preventing evaporation.[141] Biological variables include application site (e.g., scrotal skin absorbs 40 times more than forearm due to thinner SC), age (neonatal skin more permeable, elderly variably impaired), and ethnicity (darker skin may have denser SC).[141] For volatile organic compounds in water, dermal absorption can exceed ingestion in some scenarios, as skin uptake of chloroform reaches 50-80% of applied dose.[142] Formulations exploit these mechanisms; enhancers like alcohols disrupt lipids transiently, while microneedles bypass the SC entirely for macromolecules.[143] However, washing contaminated skin can induce a "wash-in" effect, mobilizing residues deeper into follicles and increasing systemic exposure by up to 10-fold in mass casualty contexts.[144] Empirical data from in vitro human skin models confirm that polar substances like water-soluble vitamins absorb minimally (<1%), underscoring the skin's efficacy as a selective barrier evolved for protection against xenobiotics.[116]Repair and Regeneration
Wound Healing Processes
Wound healing in human skin is a highly coordinated, overlapping sequence of biological events aimed at restoring barrier function and structural integrity following injury. The process typically unfolds in four phases—hemostasis, inflammation, proliferation, and remodeling—driven by cellular interactions, cytokine signaling, and extracellular matrix (ECM) deposition.[145] [146] These phases are influenced by the wound's depth, size, and location; superficial epidermal wounds regenerate with minimal scarring, while full-thickness dermal injuries result in fibrotic repair due to limited regenerative capacity in adult skin.[147] Healing generally completes in 4-6 weeks for acute wounds under optimal conditions, though remodeling persists for up to a year or more.[145] Hemostasis initiates immediately upon injury, lasting minutes to hours, to prevent blood loss and provide a provisional matrix. Vasoconstriction reduces initial bleeding, followed by platelet activation and aggregation triggered by exposure to subendothelial collagen and von Willebrand factor.[145] Platelets release alpha granules containing clotting factors, fibrinogen converts to fibrin forming a clot, and thrombin activates the coagulation cascade, stabilizing the hemostatic plug.[146] This phase transitions seamlessly into inflammation, as the clot serves as a reservoir for growth factors like platelet-derived growth factor (PDGF) and transforming growth factor-beta (TGF-β), which recruit inflammatory cells.[148] The inflammatory phase, spanning 1-4 days, clears debris and pathogens while modulating the repair environment. Neutrophils arrive first via chemotaxis, peaking within 24-48 hours to phagocytose bacteria and release reactive oxygen species and proteases.[145] Monocytes differentiate into macrophages, which dominate by day 2-3, orchestrating debris removal, angiogenesis initiation, and cytokine production (e.g., interleukin-1, tumor necrosis factor-alpha).[147] Excessive or prolonged inflammation, as in chronic wounds, impairs progression due to persistent protease activity degrading growth factors.[149] Proliferation, from days 4-21, rebuilds tissue architecture through granulation tissue formation. Fibroblasts migrate into the wound bed, synthesizing ECM components like collagen III under TGF-β stimulation, while endothelial cells form new vessels via vascular endothelial growth factor (VEGF) signaling.[146] Keratinocytes at the wound edges proliferate and migrate to re-epithelialize the surface, restoring the epidermal barrier within 48-72 hours for partial-thickness wounds.[145] Myofibroblasts contract the wound, reducing its size, though dysregulated contraction can lead to hypertrophic scars.[148] Remodeling, beginning around week 3 and extending 6-12 months or longer, refines the scar tissue for tensile strength. Collagen III is replaced by stronger collagen I fibrils through matrix metalloproteinase (MMP) activity and lysyl oxidase cross-linking, increasing strength to 70-80% of uninjured skin.[145] [147] Apoptosis reduces cellularity, and ECM reorganization minimizes fibrosis, though full regeneration without scarring is rare in adult humans due to evolutionary trade-offs favoring rapid repair over perfect fidelity.[146] Disruptions, such as diabetes-induced hypoxia or infection, prolong this phase and elevate chronic wound risk.[149]Stem Cell Roles
Stem cells in human skin are primarily resident in the basal layer of the interfollicular epidermis (IFE) and the bulge region of hair follicles, where they sustain tissue homeostasis through self-renewal and differentiation into keratinocytes.[150] These epidermal stem cells generate transit-amplifying progenitors that proliferate rapidly before terminally differentiating into the stratified layers of the epidermis, including spinous, granular, and cornified cells, thereby replacing the approximately 0.5–1 gram of dead keratinocytes shed daily from the skin surface.[151] In steady-state conditions, IFE stem cells exhibit slow cycling, often identified as label-retaining cells that divide asymmetrically every 2–4 weeks to balance proliferation with differentiation, preventing epidermal thinning or hyperproliferation.[152] Hair follicle stem cells (HFSCs), located in the bulge and associated hair germ compartments, orchestrate the periodic regeneration of hair follicles through distinct phases: anagen (growth), catagen (regression), and telogen (resting), with cycles repeating every 3–7 years in humans depending on scalp versus body hair.[153] During anagen, HFSCs activate via signaling pathways such as Wnt/β-catenin and BMP inhibition, proliferating to form the transient amplifying matrix cells that produce the hair shaft and inner root sheath.[154] These cells also contribute to sebaceous gland renewal, as bulge stem cells can give rise to sebocytes, maintaining lipid production essential for skin barrier function.30814-6) In response to injury, both IFE and HFSC populations mobilize to facilitate wound repair, with HFSCs playing a prominent role in re-epithelialization by migrating out of the follicle niche, proliferating, and differentiating into epidermal progenitors to restore barrier integrity within days of superficial wounding.[155] Studies in mouse models demonstrate that ablation of HFSCs delays epidermal closure by up to 30%, underscoring their non-redundant contribution to acute repair, particularly in full-thickness wounds where IFE stem cells alone suffice for smaller defects but require follicular support for larger ones.[154] Additionally, melanocyte stem cells in the hair follicle bulge replenish pigment-producing melanocytes during hair cycling and can aid in repigmentation post-injury, though their role diminishes with age due to niche remodeling.[156] Dermal components, including perivascular and adipose-derived stem-like cells, provide supportive roles in extracellular matrix remodeling but do not directly regenerate the epidermis.[157]Regenerative Therapies
Regenerative therapies for human skin aim to restore functional tissue architecture following injury, leveraging cellular, biomaterial, and molecular interventions to overcome limitations of natural healing, such as scarring and incomplete regeneration.[158] Stem cell-based approaches, including mesenchymal stem cells (MSCs) derived from bone marrow or umbilical cord, promote wound closure and reduce fibrosis by secreting growth factors like vascular endothelial growth factor (VEGF) and modulating inflammation.[159] In a randomized clinical trial involving cesarean section scars, intradermal injection of umbilical cord MSCs improved scar appearance and elasticity, with histological evidence of increased collagen remodeling after 6 months, though long-term efficacy requires further validation.[160] Tissue-engineered skin substitutes, such as dermal scaffolds mimicking the extracellular matrix with collagen or hyaluronic acid, integrate host cells to facilitate vascularization and epithelialization in full-thickness wounds.[161] A 2024 review of bioengineered constructs highlighted their use in chronic ulcers, where scaffolds seeded with fibroblasts and keratinocytes accelerated healing rates by 30-50% compared to standard dressings in phase II trials, attributed to enhanced angiogenesis.[159] However, challenges include immune rejection and scalability, with only select products like Apligraf (a bilayered living skin equivalent) FDA-approved for diabetic foot ulcers since 1998, demonstrating sustained epithelial coverage in 60-70% of cases.[162] Cell-free alternatives, such as platelet-rich plasma (PRP) and exosomes from MSCs, offer paracrine signaling without transplantation risks. PRP, concentrated from autologous blood, delivers growth factors to stimulate fibroblast proliferation; meta-analyses of randomized trials report 20-40% faster wound closure in burns and pressure ulcers, though variability in preparation methods limits reproducibility.[159] Exosome therapies, isolated extracellular vesicles carrying miRNAs and proteins, enhanced re-epithelialization in preclinical models by 2-fold via Wnt signaling activation, with early-phase human trials for keloid scars showing reduced hypertrophy scores at 3 months post-injection.[163][164] Ongoing clinical trials emphasize combination strategies, such as stem cells with scaffolds for extensive burns. A phase III trial (NCT04219657) comparing skin grafts alone versus grafts plus MSCs reported superior tensile strength and reduced contraction in treated wounds, with no increased adverse events over 12 months.[165] Despite promise, regulatory hurdles persist; as of 2025, FDA approvals remain limited to specific indications, with many therapies in investigational stages due to concerns over tumorigenicity and inconsistent outcomes across patient cohorts.[166] Rigorous, large-scale trials are essential to establish causal efficacy beyond anecdotal or small-sample data.[158]Pathophysiology and Disorders
Inflammatory Conditions
Inflammatory skin conditions are disorders characterized by dysregulated immune responses leading to localized inflammation, often presenting with erythema, pruritus, edema, and scaling. These conditions stem from complex interactions between genetic factors, environmental triggers, and immune dysregulation, with inflammation driven by cytokines, immune cells such as T lymphocytes and mast cells, and resident skin cells like keratinocytes.[167] Key pathophysiological mechanisms include barrier dysfunction, Th2/Th17 polarization, and mast cell degranulation, varying by disease.[168] Atopic dermatitis (AD), the most prevalent chronic inflammatory skin disease, affects over 30 million individuals in the United States alone, with global pediatric prevalence reaching 15-20%. It arises from filaggrin gene mutations impairing the epidermal barrier, allowing allergen penetration that triggers a Th2-dominant immune response, elevated IgE, and eosinophil infiltration, perpetuating a cycle of inflammation and itch-scratch damage.[169] [170] Psoriasis manifests as erythematous plaques due to autoimmune hyperproliferation of keratinocytes, mediated by IL-17 and IL-23 driven Th17 cells, with genetic associations like HLA-Cw6 contributing to susceptibility; it affects 2-3% of the population in Western countries.[167] Allergic contact dermatitis involves type IV hypersensitivity where haptens sensitize T cells, leading to cytokine release (e.g., IFN-γ) upon re-exposure, causing acute vesicular eruptions localized to contact sites.[171] Urticaria, or hives, results from mast cell and basophil degranulation releasing histamine, often via IgE-mediated or autoimmune mechanisms, producing transient wheals; chronic spontaneous urticaria persists beyond six weeks in 0.5-1% of the population.[172] These conditions highlight immune endotypes—such as type 2a eczematous in AD or type 3 psoriasiform in psoriasis—guiding targeted therapies, though environmental factors like pollutants exacerbate inflammation across types.[173]Neoplastic Diseases
Neoplastic diseases of the skin include a spectrum of tumors ranging from benign proliferations to malignant cancers originating in keratinocytes, melanocytes, or adnexal structures. The World Health Organization's 5th edition classification (2023) categorizes skin tumors by behavior: benign (non-invasive, non-metastasizing), locally aggressive intermediate (invasive but rarely metastatic), rarely metastasizing intermediate, and malignant (invasive with metastatic potential). Keratinocytic tumors dominate non-melanoma cases, while melanocytic tumors include both benign nevi and malignant melanoma.[174][175] Malignant skin neoplasms, particularly non-melanoma skin cancers (NMSC) such as basal cell carcinoma (BCC) and squamous cell carcinoma (SCC), represent the most common human cancers globally, driven primarily by ultraviolet (UV) radiation-induced DNA damage from solar exposure. In the United States, an estimated 5.4 million BCC and SCC cases are diagnosed annually, affecting approximately 3.3 million people, with BCC comprising the majority (about 80%). SCC incidence has risen up to 200% in recent decades, with roughly 1.8 million cases yearly, and age-standardized rates reaching 497 per 100,000 in men and 296 per 100,000 in women as of 2015 data trends continuing into the 2020s. Melanoma, though less common, is more lethal, with 104,960 projected new U.S. cases in 2024 (60,550 in men, 44,410 in women) and 8,430 deaths, yielding an age-adjusted incidence of 21.9 per 100,000 overall.[176][177][178] BCC arises from basal keratinocytes in the epidermis and is characterized by slow-growing, locally destructive lesions, rarely metastasizing (<0.1% of cases). Risk factors include cumulative UV exposure, fair skin phototypes (I-III), advancing age (incidence doubles from 40 to 70 years), and prior radiation therapy; indoor tanning further elevates risk via artificial UV. SCC originates from squamous keratinocytes, exhibits greater metastatic potential (2-5%), and is associated with chronic UV damage, immunosuppression, and precursor actinic keratoses. Melanoma develops from malignant transformation of melanocytes, often linked to intermittent intense UV exposure and genetic factors like fair skin or family history, with global incidence trends showing stabilization in high-income countries but persistent rises elsewhere.[179][180][181] Benign skin neoplasms, such as seborrheic keratoses or dermatofibromas, are common incidental findings but rarely require intervention unless symptomatic; they lack invasive or metastatic behavior per WHO criteria. Malignant cases demand histopathological confirmation via biopsy, with UV causation supported by epidemiological correlations: lifetime sun exposure directly correlates with mutation rates in tumor suppressor genes like TP53 in SCC and BCC, and BRAF in melanoma. Prognosis for NMSC exceeds 95% cure with early excision, contrasting melanoma's 5-year survival dropping below 30% for distant metastases.[182][183]| Type | Annual U.S. Cases (approx.) | Metastatic Risk | Primary Risk Factor |
|---|---|---|---|
| Basal Cell Carcinoma | ~4.3 million (est. from NMSC total) | <0.1% | Cumulative UV exposure[176][179] |
| Squamous Cell Carcinoma | 1.8 million | 2-5% | Chronic UV, immunosuppression[177][184] |
| Melanoma | 104,960 (2024 est.) | Up to 20% (advanced) | Intermittent UV, genetics[185][181] |
