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Mastocyte
Mast cell (large dark cell in the center of the field of view) surrounded by bone marrow cells, Giemsa stain, 1000x.
Details
SystemImmune system
Identifiers
Latinmastocytus
MeSHD008407
THH2.00.03.0.01010
FMA66784
Anatomical terms of microanatomy

A mast cell (also known as a mastocyte or a labrocyte[1]) is a resident cell of connective tissue that contains many granules rich in histamine and heparin. Specifically, it is a type of granulocyte derived from the myeloid stem cell that is a part of the immune and neuroimmune systems. Mast cells were discovered by Friedrich von Recklinghausen and later rediscovered by Paul Ehrlich in 1877.[2] Although best known for their role in allergy and anaphylaxis, mast cells play an important protective role as well, being intimately involved in wound healing, angiogenesis, immune tolerance, defense against pathogens, and vascular permeability in brain tumors.[3][4]

The mast cell is very similar in both appearance and function to the basophil, another type of white blood cell. Although mast cells were once thought to be tissue-resident basophils, it has been shown that the two cells develop from different hematopoietic lineages and thus cannot be the same cells.[5]

Structure

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Illustration depicting mast cell activation and anaphylaxis
Mast cell

Mast cells are very similar to basophil granulocytes (a class of white blood cells) in blood, in the sense that both are granulated cells that contain histamine and heparin, an anticoagulant. Their nuclei differ in that the basophil nucleus is lobated while the mast cell nucleus is round. The Fc region of immunoglobulin E (IgE) becomes bound to mast cells and basophils, and when IgE's paratopes bind to an antigen, it causes the cells to release histamine and other inflammatory mediators.[6] These similarities have led many to speculate that mast cells are basophils that have "homed in" on tissues. Furthermore, they share a common precursor in bone marrow expressing the CD34 molecule. Basophils leave the bone marrow already mature, whereas the mast cell circulates in an immature form, only maturing once in a tissue site. The site an immature mast cell settles in probably determines its precise characteristics.[7] The first in vitro differentiation and growth of a pure population of mouse mast cells was carried out using conditioned medium derived from concanavalin A-stimulated splenocytes.[8] Later, it was discovered that T cell-derived interleukin 3 was the component present in the conditioned media that was required for mast cell differentiation and growth.[9]

Mast cells in rodents are classically divided into two subtypes: connective tissue-type mast cells and mucosal mast cells. The activities of the latter are dependent on T-cells.[10]

Mast cells are present in most tissues characteristically surrounding blood vessels, nerves and lymphatic vessels,[11] and are especially prominent near the boundaries between the outside world and the internal milieu, such as the skin, mucosa of the lungs, and digestive tract, as well as the mouth, conjunctiva, and nose.[7]

Function

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The role of mast cells in the development of allergy.

Mast cells play a key role in the inflammatory process. When activated, a mast cell can either selectively release (piecemeal degranulation) or rapidly release (anaphylactic degranulation) "mediators", or compounds that induce inflammation, from storage granules into the local microenvironment.[3][12] Mast cells can be stimulated to degranulate by allergens through cross-linking with immunoglobulin E receptors (e.g., FcεRI), physical injury through pattern recognition receptors for damage-associated molecular patterns (DAMPs), microbial pathogens through pattern recognition receptors for pathogen-associated molecular patterns (PAMPs), and various compounds through their associated G-protein coupled receptors (e.g., morphine through opioid receptors) or ligand-gated ion channels.[3][12] Complement proteins can activate membrane receptors on mast cells to exert various functions as well.[7]

Mast cells express a high-affinity receptor (FcεRI) for the Fc region of IgE, the least-abundant member of the antibodies. This receptor is of such high affinity that binding of IgE molecules is in essence irreversible. As a result, mast cells are coated with IgE, which is produced by plasma cells (the antibody-producing cells of the immune system). IgE antibodies are typically specific to one particular antigen.

In allergic reactions, mast cells remain inactive until an allergen binds to IgE already coated upon the cell. Other membrane activation events can either prime mast cells for subsequent degranulation or act in synergy with FcεRI signal transduction.[13] In general, allergens are proteins or polysaccharides. The allergen binds to the antigen-binding sites, which are situated on the variable regions of the IgE molecules bound to the mast cell surface. It appears that binding of two or more IgE molecules (cross-linking) is required to activate the mast cell. The clustering of the intracellular domains of the cell-bound Fc receptors, which are associated with the cross-linked IgE molecules, causes a complex sequence of reactions inside the mast cell that lead to its activation. Although this reaction is most well understood in terms of allergy, it appears to have evolved as a defense system against parasites and bacteria.[14]

Mast cells (MCs) have been shown to release their nuclear DNA and subsequently form mast cell extracellular traps (MCETs) comparable to neutrophil extracellular traps, which are able to entrap and kill various microbes.[15]

Mast cell mediators

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A unique, stimulus-specific set of mast cell mediators is released through degranulation following the activation of cell surface receptors on mast cells.[12] Examples of mediators that are released into the extracellular environment during mast cell degranulation include:[7][12][16]

Structure of histamine

Histamine dilates post-capillary venules, activates the endothelium, and increases blood vessel permeability. This leads to local edema (swelling), warmth, redness, and the attraction of other inflammatory cells to the site of release. It also depolarizes nerve endings (leading to itching or pain). Cutaneous signs of histamine release are the "flare and wheal"-reaction. The bump and redness immediately following a mosquito bite are a good example of this reaction, which occurs seconds after challenge of the mast cell by an allergen.[7]

The other physiologic activities of mast cells are much less-understood. Several lines of evidence suggest that mast cells may have a fairly fundamental role in innate immunity: They are capable of elaborating a vast array of important cytokines and other inflammatory mediators such as TNF-α; they express multiple "pattern recognition receptors" thought to be involved in recognizing broad classes of pathogens; and mice without mast cells seem to be much more susceptible to a variety of infections.[citation needed]

Mast cell granules carry a variety of bioactive chemicals. These granules have been found to be transferred to adjacent cells of the immune system and neurons in a process of transgranulation via mast cell pseudopodia.[17]

In the nervous system

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Unlike other hematopoietic cells of the immune system, mast cells naturally occur in the human brain where they interact with the neuroimmune system.[4] In the brain, mast cells are located in a number of structures that mediate visceral sensory (e.g. pain) or neuroendocrine functions or that are located along the blood–cerebrospinal fluid barrier, including the pituitary stalk, pineal gland, thalamus, and hypothalamus, area postrema, choroid plexus, and in the dural layer of the meninges near meningeal nociceptors.[4] Mast cells serve the same general functions in the body and central nervous system, such as effecting or regulating allergic responses, innate and adaptive immunity, autoimmunity, and inflammation.[4][18] Across systems, mast cells serve as the main effector cell through which pathogens can affect the gut–brain axis.[19][20]

In the gut

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In the gastrointestinal tract, mucosal mast cells are located in close proximity to sensory nerve fibres, which communicate bidirectionally.[21][19][20] When these mast cells initially degranulate, they release mediators (e.g., histamine, tryptase, and serotonin) which activate, sensitize, and upregulate membrane expression of nociceptors (i.e., TRPV1) on visceral afferent neurons via their receptors (respectively, HRH1, HRH2, HRH3, PAR2, 5-HT3);[21] in turn, neurogenic inflammation, visceral hypersensitivity, and intestinal dysmotility (i.e., impaired peristalsis) result.[21] Neuronal activation induces neuropeptide (substance P and calcitonin gene-related peptide) signaling to mast cells where they bind to their associated receptors and trigger degranulation of a distinct set of mediators (β-Hexosaminidase, cytokines, chemokines, PGD2, leukotrienes, and eoxins).[21][12]

Physiology

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Structure of FcεR1 on mast cell. FcεR1 is a tetramer made of one alpha (α) chain, one beta (β) chain, and two gamma (γ) chains. IgE is binding to α chain, signal is transduced by ITAM motifs on β and γ chains.

Structure of the high-affinity IgE receptor, FcεR1

[edit]

FcεR1 is a high affinity IgE-receptor that is expressed on the surface of the mast cell. FcεR1 is a tetramer made of one alpha (α) chain, one beta (β) chain, and two identical, disulfide-linked gamma (γ) chains. The binding site for IgE is formed by the extracellular portion of the α chain that contains two domains that are similar to Ig. One transmembrane domain contains an aspartic acid residue, and one contains a short cytoplasmic tail.[22] The β chain contains, a single immunoreceptor tyrosine-based activation motif ITAM, in the cytoplasmic region. Each γ chain has one ITAM on the cytoplasmic region. The signaling cascade from the receptor is initiated when the ITAMs of the β and γ chains are phosphorylated by a tyrosine kinase. This signal is required for the activation of mast cells.[23] Type 2 helper T cells,(Th2) and many other cell types lack the β chain, so signaling is mediated only by the γ chain. This is due to the α chain containing endoplasmic reticulum retention signals that causes the α-chains to remain degraded in the ER. The assembly of the α chain with the co-transfected β and γ chains mask the ER retention and allows the α β γ complex to be exported to the golgi apparatus to the plasma membrane in rats. In humans, only the γ complex is needed to counterbalance the α chain ER retention.[22]

Allergen process

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Allergen-mediated FcεR1 cross-linking signals are very similar to the signaling event resulting in antigen binding to lymphocytes. The Lyn tyrosine kinase is associated with the cytoplasmic end of the FcεR1 β chain. The antigen cross-links the FcεR1 molecules, and Lyn tyrosine kinase phosphorylates the ITAMs in the FcεR1 β and γ chain in the cytoplasm. Upon the phosphorylation, the Syk tyrosine kinase gets recruited to the ITAMs located on the γ chains. This causes activation of the Syk tyrosine kinase, causing it to phosphorylate.[23] Syk functions as a signal amplifying kinase activity due to the fact that it targets multiple proteins and causes their activation.[24] This antigen stimulated phosphorylation causes the activation of other proteins in the FcεR1-mediated signaling cascade.[25]

Degranulation and fusion

[edit]

An important adaptor protein activated by the Syk phosphorylation step is the linker for activation of T cells (LAT). LAT can be modified by phosphorylation to create novel binding sites.[24] Phospholipase C gamma (PLCγ) becomes phosphorylated once bound to LAT, and is then used to catalyze phosphatidylinositol bisphosphate breakdown to yield inositol trisphosphate (IP3) and diacyglycerol (DAG). IP3 elevates calcium levels, and DAG activates protein kinase C (PKC). This is not the only way that PKC is made. The tyrosine kinase FYN phosphorylates Grb2-associated-binding protein 2 (Gab2), which binds to phosphoinositide 3-kinase, which activates PKC. PKC leads to the activation of myosin light-chain phosphorylation granule movements, which disassembles the actin–myosin complexes to allow granules to come into contact with the plasma membrane.[23] The mast cell granule can now fuse with the plasma membrane. Soluble N-ethylmaleimide sensitive fusion attachment protein receptor SNARE complex mediates this process. Different SNARE proteins interact to form different complexes that catalyze fusion. Rab3 guanosine triphosphatases and Rab-associated kinases and phosphatases regulate granule membrane fusion in resting mast cells.

MRGPRX2 mast cell receptor

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Human mast-cell-specific G-protein-coupled receptor MRGPRX2 plays a key role in the recognition of pathogen associated molecular patterns (PAMPs) and initiating an antibacterial response. MRGPRX2 is able to bind to competence stimulating peptide (CSP) 1 - a quorum sensing molecule (QSM) produced by Gram-positive bacteria.[26] This leads to signal transduction to a G protein and activation of the mast cell. Mast cell activation induces the release of antibacterial mediators including ROS, TNF-α and PRGD2 which institute the recruitment of other immune cells to inhibit bacterial growth and biofilm formation.

The MRGPRX2 receptor is a possible therapeutic target and can be pharmacologically activated using the agonist compound 48/80 to control bacterial infection.[27] It is also hypothesised that other QSMs and even Gram-negative bacterial signals can activate this receptor. This might particularly be the case during Bartonella chronic infections where it appears clearly in human symptomatology that these patients all have a mast cell activation syndrome due to the presence of a not yet defined quorum sensing molecule (basal histamine itself?). Those patients are prone to food intolerance driven by another less specific path than the IgE receptor path: certainly the MRGPRX2 route. These patients also show cyclical skin pathergy and dermographism, every time the bacteria exits its hidden intracellular location.

Enzymes

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Enzyme Function
Lyn tyrosine kinase Phosphorylates the ITAMs in the FcεR1 β and γ chain in the cytoplasm. It causes Syk tyrosine kinase to get recruited to the ITAMS located on the γ chains. This causes activation of the Syk tyrosine kinase, causing it to phosphorylate
Syk tyrosine kinase Targets multiple proteins and causes their activation
Phospholipase C Catalyzes phosphatidylinositol 4,5-bisphosphate
Inositol trisphosphate Elevates calcium levels
Diacylglycerol Activates protein kinase C
FYN Phosphorylates GAB2
GAB2 Binds to phosphoinositide 3-kinase
Phosphoinositide 3-kinase Activates protein kinase C
Protein kinase C Activates myosin light-chain phosphorylation granule movements that disassemble the actin-myosin complexes
Rab-associated kinases and phosphatases Regulate cell granule membrane fusion in resting mast cells

Clinical significance

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Parasitic infections

[edit]

Mast cells are activated in response to infection by pathogenic parasites, such as certain helminths and protozoa, through IgE signaling.[28] Various species known to be affected include T.spiralis, S.ratti, and S.venezuelensis.[28] This is accomplished via Type 2 cell-mediated effector immunity, which is characterized by signaling from IL-4, IL-5, and IL-13.[28][29] It is the same immune response that is responsible for allergic inflammation more generally, and includes effectors beyond mast cells.[28][29] In this response, mast cells are known to release significant quantities of IL-4 and IL-13 along with mast cell chymase 1 (CMA1), which is considered to help expel some worms by increasing vascular permeability.[28]

Mast cell activation disorders

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Mast cell activation disorders (MCAD) are a spectrum of immune disorders that are unrelated to pathogenic infection and involve similar symptoms that arise from secreted mast cell intermediates, but differ slightly in their pathophysiology, treatment approach, and distinguishing symptoms.[30][31] The classification of mast cell activation disorders was laid out in 2010.[30][31]

Allergic disease

[edit]

Allergies are mediated through IgE signaling which triggers mast cell degranulation.[30] Recently, IgE-independent "pseudo-allergic" reactions are thought to also be mediated via the MRGPRX2 receptor activation of mast cells (e.g. drugs such as muscle relaxants, opioids, Icatibant and fluoroquinolones).[32]

Many forms of cutaneous and mucosal allergy are mediated in large part by mast cells; they play a central role in asthma, eczema, itch (from various causes), allergic rhinitis and allergic conjunctivitis. Antihistamine drugs act by blocking histamine action on nerve endings. Cromoglicate-based drugs (sodium cromoglicate, nedocromil) block a calcium channel essential for mast cell degranulation, stabilizing the cell and preventing release of histamine and related mediators. Leukotriene antagonists (such as montelukast and zafirlukast) block the action of leukotriene mediators and are being used increasingly in allergic diseases.[7]

Calcium triggers the secretion of histamine from mast cells after previous exposure to sodium fluoride. The secretory process can be divided into a fluoride-activation step and a calcium-induced secretory step. It was observed that the fluoride-activation step is accompanied by an elevation of cyclic adenosine monophosphate (cAMP) levels within the cells. The attained high levels of cAMP persist during histamine release. It was further found that catecholamines do not markedly alter the fluoride-induced histamine release. It was also confirmed that the second, but not the first, step in sodium fluoride-induced histamine secretion is inhibited by theophylline.[33] Vasodilation and increased permeability of capillaries are a result of both H1 and H2 receptor types.[34]

Stimulation of histamine activates a histamine (H2)-sensitive adenylate cyclase of oxyntic cells, and there is a rapid increase in cellular [cAMP] that is involved in activation of H+ transport and other associated changes of oxyntic cells.[35]

Anaphylaxis

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In anaphylaxis (a severe systemic reaction to allergens, such as nuts, bee stings, or drugs), the body-wide degranulation of mast cells leads to vasodilation and, if severe, symptoms of life-threatening shock.[36][37] Products released from these granules include histamine, serotonin, heparin, chondroitin sulphate, tryptase, chymase, carboxypeptidase, and TNF-α.[36] These can vary in their quantities and proportions between individuals, which may explain some of the differences in symptoms seen across patients.[36]

Histamine is a vasodilatory substance released during anaphylaxis.[34]

Autoimmunity

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Mast cells may be implicated in the pathology associated with autoimmune, inflammatory disorders of the joints. They have been shown to be involved in the recruitment of inflammatory cells to the joints (e.g., rheumatoid arthritis) and skin (e.g., bullous pemphigoid), and this activity is dependent on antibodies and complement components.[38]

Mastocytosis and clonal disorders

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Mastocytosis is a rare clonal mast cell disorder involving the presence of too many mast cells (mastocytes) and CD34+ mast cell precursors.[39] Mutations in c-Kit are associated with mastocytosis.[30] More specifically, the majority (>80%) of patients with mastocytosis have a mutation at codon 816 in the kinase domain of KIT, known as the KIT D816V mutation.[40][41] This mutation, as well as expression of either CD2 or CD25 (confirmed by immunostaining or flow cytometry), are characteristic of primary clonal/monoclonal mast cell activation syndrome (CMCAS/MMAS).[41] The most commonly affected organs in mastocytosis are the skin and bone marrow.[42]

Monoclonal disorders

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Neoplastic disorders

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Mastocytomas, or mast cell tumors, can secrete excessive quantities of degranulation products.[30][31] They are often seen in dogs and cats.[43] Other neoplastic disorders associated with mast cells include mast cell sarcoma and mast cell leukemia.

Mast cell activation syndrome

[edit]

Mast cell activation syndrome (MCAS) is an idiopathic immune disorder that involves recurrent and excessive mast cell degranulation and which produces symptoms that are similar to other mast cell activation disorders.[30][31] The syndrome is diagnosed based upon four sets of criteria involving treatment response, symptoms, a differential diagnosis, and biomarkers of mast cell degranulation.[30][31]

History

[edit]

Mast cells were first described by Paul Ehrlich in his 1878 doctoral thesis on the basis of their unique staining characteristics and large granules. These granules also led him to the incorrect belief that they existed to nourish the surrounding tissue, so he named them Mastzellen (from German Mast 'fattening', as of animals).[44][45] They are now considered to be part of the immune system.

Research

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Autism

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Research into an immunological contribution to autism suggests that autism spectrum disorder (ASD) children may present with "allergic-like" problems in the absence of elevated serum IgE and chronic urticaria, suggesting non-allergic mast cell activation in response to environmental and stress triggers. This mast cell activation could contribute to brain inflammation and neurodevelopmental problems.[46]

Histological staining

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Toluidine blue: one of the most common stains for acid mucopolysaccharides and glycoaminoglycans, components of mast cells granules.[47]

Bismarck brown: stains mast cell granules brown.[48]

Surface markers: cell surface markers of mast cells were discussed in detail by Heneberg,[49] claiming that mast cells may be inadvertently included in the stem or progenitor cell isolates, since part of them is positive for the CD34 antigen. The classical mast cell markers include the high-affinity IgE receptor, CD117 (c-Kit), and CD203c (for most of the mast cell populations). Expression of some molecules may change in course of the mast cell activation.[50]

Heterogeneity

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Mast cell heterogeneity significantly impacts the efficacy of mast cell stabilizing drugs disodium cromoglycate and ketotifen in preventing mediator release. In experiments, ketotifen inhibits mast cells from lung and tonsillar tissues when stimulated via an IgE-dependent histamine release mechanism, while disodium cromoglycate is less effective but still inhibited these mast cells. However, both agents fail to inhibit mediator release from skin mast cells, indicating that these cells are unresponsive to these stabilizers. Such differences in mast cell activation suggests the existence of different mast cell types across various tissues—a topic of ongoing research.[51][52]

Other organisms

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Mast cells and enterochromaffin cells are the source of most serotonin in the stomach in rodents.[53]

See also

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References

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[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Mast cell

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from Grokipedia
Mast cells are long-lived, tissue-resident immune cells of hematopoietic origin, derived from myeloid progenitors in the , and are distinguished by their abundant cytoplasmic granules containing preformed mediators such as , , , and chymase. They mature and reside primarily at host-environment interfaces, including the skin, mucosa of the respiratory and gastrointestinal tracts, and near blood vessels and nerves, positioning them to respond rapidly to external threats. Upon activation through receptors like FcεRI (for IgE-mediated responses) or other receptors, mast cells undergo , selectively releasing granule contents along with newly synthesized mediators such as cytokines, , and leukotrienes, which orchestrate immediate reactions and . These cells play pivotal roles in innate immunity by defending against parasites, bacteria, and venoms, while also modulating adaptive immune responses, , , and tissue remodeling. In addition to protective functions, mast cells contribute to immunoregulation, potentially suppressing excessive or promoting tolerance in certain contexts, though their dysregulation is implicated in allergic disorders like and , autoimmune diseases, and malignancies such as mast cell tumors. Two major subtypes exist based on content: -positive mucosal mast cells (MC_T), predominant in mucosal tissues, and chymase-, -, and carboxypeptidase A-positive mast cells (MC_TC), found in connective tissues.

Structure and Morphology

Cellular Composition

Mast cells are long-lived, tissue-resident granulocytes that originate from committed progenitors in the , which migrate to peripheral tissues and mature locally under the influence of microenvironmental factors. These cells play a central role in immune responses, distinguished by their granular and capacity for rapid mediator release. At the ultrastructural level, mast cells feature a prominent irregular or folded nucleus, often eccentric, surrounded by abundant filled with large, electron-dense secretory granules that dominate the cellular architecture. These granules, numbering from hundreds to thousands per cell, contain preformed mediators such as (a ), (a ), and (a ), which are packaged within a complex matrix visible under electron microscopy. An extensive Golgi apparatus is evident, facilitating the synthesis, modification, and packaging of granule contents, including lysosomal enzymes and cytokines, into these specialized organelles. Mast cells express key surface markers that define their identity and function, including the tyrosine kinase receptor c-Kit (also known as CD117), which is essential for their survival and differentiation, and the high-affinity IgE receptor FcεRI, which confers sensitivity to IgE-mediated activation. These receptors are constitutively expressed on the cell surface, enabling interactions with (for c-Kit) and allergen-bound IgE (for FcεRI). Morphologically, mature mast cells are typically round or spindle-shaped, measuring 10–20 μm in diameter, with variations depending on tissue location and activation state. Their granules exhibit metachromatic staining properties when treated with basic dyes like , appearing purple or red due to the polyanionic nature of and other components, which shifts the dye's color from blue—a hallmark for histological identification.

Tissue Distribution and Heterogeneity

Mast cells are distributed throughout the body, with a particular abundance in connective tissues and at mucosal surfaces exposed to the external environment, such as the skin, , , and lungs. They are also commonly found in close proximity to blood vessels and , reflecting their strategic positioning for rapid response to environmental stimuli. This widespread localization underscores their role as sentinel cells in various tissues, where their density can vary significantly depending on the organ and physiological state. In , mast cells display pronounced phenotypic heterogeneity, primarily classified into two subtypes based on their tissue residency: mast cells (CTMCs) and mucosal mast cells (MMCs). CTMCs predominate in subcutaneous tissues, , and other connective tissue-rich areas, while MMCs are enriched in the mucosal linings of the intestine and airways. These subtypes differ in morphology, with CTMCs being larger and more granular, and in their biochemical composition, particularly the proteoglycans within their secretory granules—CTMCs contain predominantly , whereas MMCs are characterized by higher levels of . This granule diversity correlates closely with their respective tissue environments and influences their storage and release capabilities. Mast cell heterogeneity arises largely from adaptations to the local microenvironment, which shapes their maturation, survival, and functional properties post-differentiation from progenitors. Key factors include tissue-specific cytokines and growth factors; for instance, (SCF), produced by fibroblasts and other stromal cells, is essential for mast cell survival, proliferation, and in diverse niches. Variations in SCF availability and other local signals contribute to the observed diversity in mediator content and responsiveness across tissues. Unlike the clear CTMC/MMC dichotomy in , human mast cells exhibit a more nuanced heterogeneity without a strict equivalent classification, instead showing tissue-dependent variations primarily in expression. Human mast cells are categorized as -only (MCT), chymase-only (MCC), or those expressing both and chymase (MCTC), with MCT cells more prevalent in and intestinal mucosa, while MCTC predominate in and other connective tissues. This profile reflects site-specific adaptations, as chymase expression is notably lower in pulmonary and gastrointestinal mast cells compared to those in the , highlighting interspecies differences in phenotypic organization.

Function and Activation

Mediator Release Mechanisms

Mast cells release preformed and newly synthesized mediators through distinct processes, primarily triggered by receptor cross-linking such as that of the high-affinity IgE receptor FcεRI. Anaphylactic is a rapid, IgE-mediated event characterized by compound , where multiple secretory granules fuse with each other and the plasma membrane to release , proteases, and other preformed mediators within seconds to minutes. This process involves sequential stages: initial receptor cross-linking activates signaling cascades leading to intracellular calcium influx from stores and extracellular sources, which then promotes complex formation (including syntaxin, SNAP-23, and VAMP) to mediate granule docking and fusion with the plasma membrane. In contrast, piecemeal represents a slower, selective mechanism where individual granules progressively lose contents via small vesicular transport to the plasma , allowing sustained release of mediators without full granule ; this mode is often observed in chronic inflammation and involves tubulovesicular structures for cargo packaging and delivery. Transgranulation occurs when mast cells transfer intact granule contents directly to adjacent cells through fusion or capture of granule remnants, facilitating intercellular exchange, as demonstrated in interactions with neurons or fibroblasts. Newly synthesized mediators are generated post-activation and released over minutes to hours. Lipid-derived mediators include prostaglandins such as PGD2, produced via the pathway from , and leukotrienes like LTC4 and LTB4, synthesized through the 5-lipoxygenase (5-LOX) pathway following activation. Cytokines, including IL-4 and TNF-α, are transcribed and secreted following activation of transcription factors like and AP-1, contributing to prolonged inflammatory signaling. Mast cells also employ non-degranulation pathways for mediator release, particularly for cytokines, involving vesicular independent of classical granule ; for instance, stimuli like IL-1 or TSLP induce IL-6 or other cytokines via distinct intracellular trafficking routes without triggering release or calcium-dependent fusion. Mast cells exhibit clock-dependent circadian rhythms in activity, with histamine release showing rhythmic patterns regulated by the intrinsic molecular clock. Recent studies as of 2025 have further elucidated functional heterogeneity in these activation pathways, with tissue-specific differences in mediator responses.

Physiological Roles in Immunity

Mast cells contribute to innate immunity by providing early defense against bacterial and through the release of stored in their granules. These include cathelicidins such as LL-37 in humans and in mice, which exhibit activity by disrupting microbial membranes and inhibiting growth. For instance, skin mast cells protect against by activating the receptor S1PR2, leading to and peptide release that limits . Additionally, mast cell-derived proteases like and chymase enhance antimicrobial effects by cleaving bacterial components and promoting by other immune cells. In bridging innate and adaptive immunity, mast cells facilitate the enhancement of IgE-mediated responses and the recruitment of key effector cells. Upon activation by pathogens or allergens, mast cells produce chemokines such as TNF-α and IL-8, which attract and neutrophils to sites, amplifying the inflammatory response. They also present antigens via molecules, promoting Th2 cell differentiation and subsequent B-cell production of IgE antibodies, thereby linking immediate innate defenses to long-term . This immunomodulatory role positions mast cells as sentinels that orchestrate coordinated immune activation without relying solely on IgE pathways. Mast cells promote and by secreting growth factors and mediators that support tissue repair. released from mast cell granules increases , allowing plasma proteins and immune cells to extravasate into the site, which facilitates clot formation and debris clearance. Furthermore, mast cells produce (VEGF), which stimulates endothelial and new blood vessel formation essential for delivering oxygen and nutrients during healing. Proteases like also activate matrix metalloproteinases, aiding in remodeling and fibroblast migration. In homeostatic functions, mast cells regulate vascular tone and maintain epithelial barrier integrity. Through release of and other vasoactive mediators, they modulate endothelial cell contractility, ensuring appropriate blood flow and preventing excessive permeability under normal conditions. Mast cells also support epithelial barriers by producing TGF-β, which promotes formation and differentiation, thereby preserving tissue integrity against environmental challenges. This balanced activity underscores their role in physiological maintenance beyond acute responses.

Role in Specific Systems

Involvement in Nervous System

Mast cells are predominantly localized in the perivascular spaces and of the , where they reside on the abluminal side of blood vessels, allowing close interactions with neurons, , , and the . In these strategic positions, approximately 97% of brain mast cells are situated to communicate directly with neural and glial components without crossing the blood-brain barrier. This perivascular and meningeal distribution facilitates their role in neuro-immune surveillance and response to local stimuli. In neuroinflammatory processes, mast cells contribute by releasing mediators such as and serotonin, which modulate sensory perceptions including and through activation of peripheral endings and central neural pathways. Recent studies as of 2025 have highlighted the mast cell-neuron axis as a key mechanism in chronic pruritus, orchestrating bidirectional neuroimmune crosstalk that amplifies itch signaling. from degranulated mast cells enhances sensitivity and promotes pruritus via on sensory neurons, while serotonin similarly influences signaling and vascular responses. Additionally, these mediators increase blood-brain barrier permeability by inducing endothelial changes and activity, thereby allowing immune cell infiltration during . Mast cells engage in bidirectional signaling with the , where neuropeptides like , released from terminals, directly activate mast cells via receptors such as MRGPRX2, triggering and mediator release. This activation amplifies neurogenic inflammation, characterized by , plasma extravasation, and recruitment of additional immune cells, creating a feedback loop that sustains neural-immune crosstalk. Mast cells have been implicated in neurological conditions such as migraines, where meningeal mast cells release inflammatory mediators that contribute to pain pathways and vascular changes, and , through their role in promoting and demyelination processes in the .

Involvement in Gastrointestinal Tract

Mast cells are densely distributed throughout the , residing primarily in the mucosal and layers, where they serve as sentinels for immune surveillance. Their abundance is notably higher in the of the small and large intestines, with elevated densities reported in the and colon compared to other segments such as the or . In the ileocecal , for instance, mast cell counts can reach up to 110 per square millimeter in the , underscoring their strategic positioning to monitor luminal contents and maintain barrier integrity. This distribution reflects their adaptation to the unique immunological demands of the gut environment, including exposure to dietary antigens and commensal microbes. In gut immunity, mast cells play critical roles in preventing food allergies and facilitating expulsion through targeted mediator release. Upon activation, they secrete , which modulates intestinal to enhance the expulsion of helminth parasites, thereby contributing to host defense against infections. Additionally, mast cells promote epithelial repair by producing transforming growth factor-β (TGF-β), a that stimulates activity and extracellular matrix deposition to restore mucosal integrity following injury or . These functions help avert excessive immune responses to harmless food antigens, supporting the balance between tolerance and protection in the intestinal mucosa. Recent research as of has further elucidated their involvement in digestive system tumors, where mast cells influence tumor progression and responses. Mast cells also interact dynamically with the gut microbiota, sensing microbial patterns via Toll-like receptors (TLRs) expressed on their surface, such as TLR2, TLR4, and TLR5. This sensing enables them to modulate inflammatory responses; for example, commensal can suppress mast cell through TLR-dependent pathways, preventing unwarranted activation. In states of , however, hyperactivated mast cells release pro-inflammatory mediators like and cytokines, exacerbating gut and contributing to conditions such as . These interactions highlight mast cells' role in maintaining microbial and mitigating dysbiosis-related pathology. Furthermore, mast cells contribute to oral tolerance induction by secreting regulatory cytokines, including TGF-β and interleukin-10 (IL-10), which foster an milieu conducive to immune hyporesponsiveness toward dietary antigens. Desensitized mast cells, in particular, enhance function during oral , promoting long-term tolerance through increased production of these suppressive factors. This mechanism supports the gut's ability to distinguish benign food components from threats, preventing allergic while preserving protective immunity. Advances in intestinal as of 2025 underscore mast cells' integration with neural signals in pathogenesis.

Molecular Mechanisms

High-Affinity IgE Receptor (FcεRI)

The high-affinity (IgE) receptor, FcεRI, is a tetrameric transmembrane complex consisting of one α subunit, one β subunit, and two disulfide-linked γ subunits (αβγ₂). The α chain, which spans the plasma membrane once, contains two extracellular immunoglobulin-like domains responsible for binding the Fc portion of IgE with an affinity constant in the range of 10⁹ to 10¹⁰ M⁻¹. The β and γ chains are multi-spanning membrane proteins that lack extracellular domains but possess intracellular immunoreceptor tyrosine-based activation motifs (ITAMs) essential for . This structure enables FcεRI to function as the primary receptor for IgE-mediated activation on mast cells. FcεRI is predominantly expressed on the surface of mast cells and , where it exists at high density—up to 300,000 receptors per cell on mature mast cells—facilitating rapid responses to allergens. Expression levels are dynamically regulated; binding of IgE to the α chain stabilizes the receptor complex, preventing its internalization and degradation, thereby increasing surface expression by up to 3- to 5-fold in proportion to serum IgE concentrations. This stabilization is particularly pronounced in mast cells, enhancing their sensitivity to environmental antigens without altering the receptor's intrinsic signaling capacity. Upon antigen-induced cross-linking of IgE-bound FcεRI, receptor aggregation triggers rapid of the ITAMs on the β and γ chains by the Lyn, which is pre-associated with the receptor's intracellular domain. Phosphorylated ITAMs serve as docking sites for the tandem SH2 domains of the Syk , leading to its through autophosphorylation and recruitment of proteins. Activated Syk then phosphorylates and activates Cγ (PLCγ), which cleaves (PIP₂) into inositol 1,4,5-trisphosphate (IP₃) and diacylglycerol (DAG); IP₃ subsequently binds to receptors on the , mobilizing intracellular calcium stores and initiating a sustained calcium influx essential for downstream mast cell responses. This cascade, initiated within seconds of cross-linking, exemplifies the receptor's role as a finely tuned for immune challenges. Structural studies from the late 1990s and early 2000s have provided atomic-level insights into FcεRI's interactions. The of the extracellular portion of the α chain, determined at 2.4 resolution in , revealed a bent conformation with two C2-type immunoglobulin domains, where the membrane-proximal domain features a unique loop that contributes to IgE specificity. A landmark 2000 study at 3.8 resolution captured the complex of the α chain with the Fc fragment of IgE (Fcε3-4), demonstrating a 1:1 with the receptor's D1 domain engaging the IgE Cε3 domain through hydrophobic and electrostatic interactions, burying over 1,400 ² of solvent-accessible surface area and distorting the IgE structure to prevent simultaneous binding to low-affinity receptors like CD23. These findings, derived from of recombinant proteins, underscore the receptor's evolutionary adaptation for high-affinity, stable IgE capture on mast cell surfaces.

Degranulation and Fusion Processes

Degranulation in mast cells involves the regulated of secretory granules, a process driven by the fusion of intracellular vesicles with the plasma membrane. This is orchestrated by a complex molecular machinery that ensures rapid and controlled release of preformed mediators upon cellular activation. The core of this machinery consists of SNARE proteins, which form a trans-SNARE complex to bridge and fuse granule and plasma membranes. Specifically, the t-SNAREs syntaxin-4 and SNAP-23 on the plasma membrane pair with the v-SNARE VAMP-7 on the granule membrane to mediate fusion during . Rab GTPases, such as Rab37 and Rab44, play crucial roles in granule trafficking and docking prior to fusion, facilitating the movement of granules to the cell periphery and their priming for . The fusion process is highly dependent on calcium ions, which act as a key trigger for . Upon mast cell activation, typically via cross-linking of IgE-bound FcεRI receptors, store-operated calcium entry occurs through CRAC channels, primarily composed of Orai1 and regulated by STIM1, leading to a sustained rise in cytosolic calcium levels. This calcium influx recruits and activates synaptotagmin isoforms, such as synaptotagmin-2, which serve as calcium sensors that bind to the SNARE complex in a calcium-dependent manner, promoting fusion. Kinetically, proceeds rapidly, with granule fusion initiating within seconds of calcium elevation, enabling swift mediator discharge. Mast cells exhibit two primary modes of : partial exocytosis, where individual granules fuse directly with the plasma membrane, and compound exocytosis, involving sequential fusion of granules with one another before plasma membrane integration, which amplifies release efficiency. Regulation of includes inhibitory mechanisms to prevent excessive . Siglec-8 engagement recruits phosphatases that dampen proximal signaling, thereby suppressing fusion events. Similarly, dysregulation of LAT can inhibit downstream events leading to , as LAT serves as a critical adaptor in the signaling cascade that culminates in granule release.

MRGPRX2 Receptor and Non-IgE Activation

The MRGPRX2 receptor, a member of the mas-related (MRGPR) family, is a seven-transmembrane (GPCR) primarily expressed on the surface of human mast cells, with notable abundance in and tissues. This expression pattern positions it as a key mediator of localized immune responses in barrier tissues. Unlike classical GPCRs, MRGPRX2 exhibits promiscuous ligand binding, responding to diverse cationic molecules that lack structural homology, which enables rapid and direct activation of mast cells independent of (IgE). Upon ligand binding, MRGPRX2 triggers intracellular signaling through dissociation, leading to the activation of (PLC) and subsequent production of (IP3), which mobilizes intracellular calcium stores to initiate and mediator release. A of this pathway is the recruitment of β-arrestin, which not only desensitizes the receptor but also facilitates additional downstream effects like cytoskeletal rearrangements, contrasting with the ITAM-dependent signaling in IgE-mediated activation via FcεRI. This β-arrestin-mediated mechanism allows for sustained signaling in some contexts, amplifying mast cell responses without requiring co-receptors. Diverse ligands activate MRGPRX2, including neuropeptides such as substance P, antimicrobial peptides like LL-37, host defense peptides from venoms (e.g., mastoparan), and synthetic compounds like certain antibiotics (e.g., ciprofloxacin) and neuromuscular blocking agents. These interactions often occur at subnanomolar to micromolar concentrations, underscoring the receptor's high sensitivity to environmental and pharmacological triggers. In physiological contexts, MRGPRX2 activation contributes to pseudo-allergic reactions, where mast cell degranulation mimics allergic responses but bypasses adaptive immunity, facilitating immediate defense against pathogens or irritants at mucosal surfaces. Species-specific differences are prominent, as MRGPRX2 is uniquely and absent in ; its functional ortholog, Mrgprb2, is expressed on mast cells but responds selectively to a subset of ligands, such as compound 48/80, limiting direct translational models for studies. This divergence complicates preclinical research but highlights MRGPRX2's specialized role in pseudo-allergic hypersensitivity, where it drives rapid mast cell responses to drugs and toxins without prior sensitization.

Key Enzymes and Mediators

Mast cells store several preformed mediators in their granules, which are released rapidly upon activation through . , a key , is synthesized from L-histidine via the enzyme and stored in high concentrations within mast cell granules. Among the proteases, is the most abundant in human mast cells, comprising up to 50% of the total protein content in secretory granules. Chymase, another , is predominantly found in mast cells and constitutes about 20-30% of granule protein. Carboxypeptidase A3 (CPA3), a metalloexopeptidase, is also pre-stored and specific to mast cells, aiding in the processing of other mediators. These proteases exert enzymatic effects beyond mere release. activates (PAR-2) by cleaving its N-terminal exodomain, initiating signaling cascades in target cells. Chymase cleaves I to generate II, contributing to local vasoactive responses independent of the classical renin- system. Upon activation, mast cells also synthesize lipid mediators de novo from . (PGD2) is primarily produced via cyclooxygenase-1 (COX-1) in the immediate phase of activation, with COX-2 contributing to sustained production in certain contexts. C4 (LTC4), a potent cysteinyl , is generated through the 5-lipoxygenase pathway, where 5-lipoxygenase-activating protein (FLAP) facilitates A4 synthesis, followed by conjugation with by LTC4 synthase. Mast cells produce a range of cytokines, with distinct storage and synthesis patterns. Tumor necrosis factor-alpha (TNF-α) is pre-stored in granules for rapid release, enabling immediate proinflammatory effects. In contrast, interleukin-6 (IL-6) and interleukin-13 (IL-13) are synthesized de novo following activation, supporting Th2-type immune responses over extended periods.

Clinical Significance

Role in Parasitic Infections and Allergies

Mast cells play a crucial role in the immune defense against parasitic infections, particularly helminths, through IgE-mediated mechanisms that facilitate worm expulsion. Upon recognition of parasite antigens, IgE antibodies bind to the high-affinity IgE receptor (FcεRI) on mast cell surfaces, triggering and release of mediators such as and leukotrienes. These mediators induce intestinal and mucus hypersecretion, which are essential for expelling gastrointestinal nematodes like Nippostrongylus brasiliensis. In experimental models, mast cell-deficient mice exhibit delayed worm clearance, underscoring the cells' protective function in this process. In allergic responses, mast cells contribute to Th2-skewed immune reactions that evolved partly as an adaptation to multicellular parasites. The activation of mast cells amplifies recruitment via the secretion of like CCL11 (eotaxin), promoting a coordinated environment that enhances parasite clearance but can become maladaptive in non-infectious contexts. This Th2 polarization is evident in conditions where exposure mimics parasitic antigens, leading to mast cell and sustained . Mast cells are central to reactions, initiating immediate allergic responses through rapid mediator release upon cross-linking of IgE-FcεRI complexes. The late-phase response involves further recruitment of inflammatory cells, including and T cells, which can cross-talk with Type IV delayed pathways via production like IL-4 and TNF-α. From an evolutionary standpoint, mast cells are considered ancient sentinels adapted to combat multicellular parasites, with homologs present in non-mammalian vertebrates that similarly mediate IgE-like responses against helminths. This conserved role highlights their dual-edged function: protective against infections yet prone to in modern environments lacking such threats.

Mast Cell Activation Disorders

Mast cell activation disorders encompass a range of non-clonal conditions characterized by inappropriate or excessive mast cell , leading to the release of mediators such as , leukotrienes, and cytokines that drive multisystem symptoms. These disorders arise from dysregulated activation pathways, often IgE-dependent in allergic contexts or triggered by non-immunologic stimuli, resulting in acute or chronic inflammation without underlying mast cell proliferation. Unlike neoplastic conditions, they involve functional hyperactivity of normal mast cell numbers, contributing to a spectrum of reactions. In allergic diseases, mast cells play a central role through chronic activation mechanisms, particularly in responses. In , allergen exposure cross-links IgE on mast cell surfaces via FcεRI, prompting and mediator release that cause , hypersecretion, and airway remodeling over time; persistent Th2-driven sustains this cycle. Similarly, in allergic rhinitis, nasal mast cells respond to aeroallergens like , releasing and to induce sneezing, itching, and , with chronic exposure leading to epithelial damage and recruitment. Atopic dermatitis involves skin-resident mast cells activated by environmental triggers or scratching-induced pseudoallergens, promoting itch-scratch cycles via protease-activated receptor-2 (PAR-2) signaling and chronic barrier disruption. Anaphylaxis represents a severe, systemic form of mast cell activation, involving rapid that affects multiple organs including the skin, respiratory, cardiovascular, and gastrointestinal systems. Common triggers include foods such as , tree nuts, and , which elicit IgE-mediated responses, as well as drugs like beta-lactam antibiotics and nonsteroidal anti-inflammatory drugs (NSAIDs) that can provoke either IgE-dependent or direct activation via MRGPRX2 receptors. Biphasic reactions occur in up to 20% of cases, with a second wave of symptoms emerging 4 to 12 hours after the initial episode due to prolonged mediator effects or late-phase recruitment of additional inflammatory cells. First-line treatment is intramuscular epinephrine, which reverses and by stimulating α- and β-adrenergic receptors to counteract mast cell mediator actions. Mast cells contribute to autoimmune diseases by amplifying and autoantigen presentation through activity. In , synovial mast cells degranulate in response to immune complexes, releasing and chymase that cleave components into neoantigens, thereby enhancing T-cell activation and joint destruction. In systemic lupus erythematosus, mast cells infiltrate affected tissues and produce that process self-proteins, such as histones, into immunogenic fragments that promote production and immune complex deposition. Idiopathic anaphylaxis manifests as recurrent episodes of without identifiable triggers, classified as a form of mast cell activation syndrome (MCAS) where episodic mediator release causes symptoms like and urticaria in the absence of clonal mast cell abnormalities. Hereditary alpha-tryptasemia, an autosomal dominant trait affecting 4-6% of populations, involves multiple copies of the TPSAB1 gene leading to elevated baseline serum levels (often >8 ng/mL), which predisposes individuals to heightened mast cell reactivity and MCAS-like symptoms including flushing, , and anaphylactoid reactions. Mastocytosis encompasses a group of clonal mast cell proliferative disorders characterized by abnormal accumulation and activation of mast cells in various tissues, leading to diverse clinical manifestations ranging from benign skin lesions to life-threatening systemic involvement. These conditions arise from neoplastic transformation of mast cell precursors, often driven by somatic mutations in the KIT gene, which encodes the c-Kit receptor tyrosine kinase essential for mast cell development and survival. In its 2022 fifth edition, the World Health Organization (WHO) classifies mastocytosis into distinct variants based on clinical behavior, organ involvement, and histopathological features, emphasizing the need for precise diagnosis to guide management. Cutaneous mastocytosis (CM) is confined to the skin and typically presents in children with lesions such as , where mast cells infiltrate the without systemic spread. In contrast, systemic mastocytosis (SM) involves extracutaneous organs, most commonly the bone marrow, , liver, and , and predominates in adults. SM is further subdivided into indolent systemic mastocytosis (ISM), the most frequent subtype accounting for about two-thirds of cases, which is often or mildly symptomatic without organ dysfunction; smoldering SM (SSM), marked by higher mast cell burden and elevated markers but still indolent; and aggressive forms including aggressive systemic mastocytosis (ASM), systemic mastocytosis with an associated hematologic neoplasm (SM-AHN), and mast cell leukemia (MCL). Aggressive variants like ASM and MCL are rare but progressive, featuring organ damage such as cytopenias, , or osteolysis due to extensive mast cell infiltration. The genetic hallmark of mastocytosis is the activating point mutation in exon 17 of the KIT gene, resulting in the aspartate-to-valine substitution at codon 816 (KIT D816V), which confers ligand-independent receptor dimerization and constitutive signaling, promoting uncontrolled mast cell proliferation. This mutation is detected in 80-90% of adult SM cases and up to 95% of advanced subtypes, though it is less common in pediatric CM (around 25-75% in skin lesions). Other KIT mutations or variants may occur but are rarer, highlighting KIT D816V's central role in disease pathogenesis. Diagnosis relies on the WHO criteria, requiring either the major criterion of multifocal dense infiltrates of at least 15 mast cells in bone marrow or other extracutaneous tissues, plus one minor criterion such as atypical mast cell morphology (>20% spindle-shaped or immature forms), expression of aberrant markers like CD25 or CD2, presence of KIT D816V or other activating KIT mutations, or persistently elevated serum total tryptase levels exceeding 20 ng/mL. Bone marrow biopsy is essential for confirming SM, revealing characteristic infiltrates and aiding subtyping, while serum tryptase serves as a sensitive, non-invasive marker correlating with mast cell burden—levels above 20 ng/mL strongly support the diagnosis and predict poorer prognosis in aggressive forms. Molecular testing for KIT D816V in bone marrow or peripheral blood enhances diagnostic accuracy, particularly in indolent cases. Beyond core mastocytosis variants, related neoplastic conditions include mast cell leukemia, a leukemic phase of SM defined by ≥20% circulating mast cells or absolute count >1 × 10^9/L, often with rapid progression and poor survival, and mast cell sarcoma, an exceedingly rare, highly aggressive tumor of solid mast cell masses lacking systemic involvement. These entities frequently harbor KIT D816V and may associate with other hematologic malignancies in SM-AHN, such as myelodysplastic syndromes or . Treatment strategies vary by subtype and risk; indolent forms like and CM often require only symptom management with antihistamines or cytoreductive agents like interferon-alpha, whereas aggressive SM, MCL, and sarcomas demand targeted therapies. Midostaurin, a multi-tyrosine inhibitor approved by the FDA in 2017 for advanced SM including ASM, SM-AHN, and MCL, potently inhibits KIT D816V-driven signaling, achieving major responses in 50-75% of patients by reducing mast cell burden and improving organ function, though it does not eradicate the . , a more selective KIT D816V inhibitor approved by the FDA in 2021 for advanced systemic mastocytosis and in 2023 for indolent systemic mastocytosis, has emerged as an alternative for non-responders, demonstrating high response rates in relapsed cases. Allogeneic transplantation remains an option for eligible patients with high-risk disease.

History and Discovery

Early Observations

Mast cells, termed "Mastzellen" by , were first identified in 1878 during his doctoral thesis at , where he described these granulated cells in connective tissues surrounding blood vessels based on their distinctive staining properties with basic s. Ehrlich noted the cells' large, metachromatic granules, which shifted from the dye's original blue color to purple, suggesting they contained a substance capable of altering dye spectra, and he proposed they functioned in nutrient storage, appearing "fattened" or well-nourished hence the name. Early characterizations viewed mast cells primarily as secretory elements involved in local tissue or , with little recognition of their potential immune roles, as histological studies in the late 19th and early 20th centuries focused on their abundance in connective tissues without linking them to defensive functions. For granule visualization, initial techniques relied on aniline-based stains like , but by the early 1900s, metachromatic dyes such as toluidine blue—introduced by Ehrlich in 1878—and , developed in 1904, became key for highlighting the purple-violet granules, enabling clearer identification in fixed tissues. In the and extending into the , research on reactions began to emerge, notably with Paul Portier and Charles Richet's 1902 description of in dogs sensitized to toxin, a phenomenon they termed to denote its oppositional nature to prophylaxis, earning them the 1913 in Physiology or Medicine. Although early studies on emphasized humoral factors like serum antibodies, these observations laid groundwork for later connections to cellular mediators, including mast cells, as investigations into shock mechanisms progressed.

Key Milestones in Research

In the 1960s, Kimishige and Teruko Ishizaka discovered (IgE), identifying it as the fifth class of immunoglobulins responsible for reaginic activity in allergic reactions. Their seminal work demonstrated that IgE binds to specific receptors on and , triggering and mediator release upon exposure. This breakthrough, detailed in a series of publications, established IgE as the key mediator of and laid the foundation for understanding mast cell involvement in allergies. Building on this, the Ishizakas characterized the high-affinity IgE receptor (FcεRI) in the early 1970s, confirming its expression on mast cells as the primary binding site for IgE and its role in initiating allergic responses. During the and , further molecular advances included the cloning of the KIT proto-oncogene in 1987, which encodes the essential for mast cell survival, proliferation, and differentiation in response to . Concurrently, was recognized as a highly specific enzymatic marker for mast cells, with studies showing its exclusive storage and release from mast cell granules, enabling precise identification and quantification in tissues and serum. In the 2000s, the identification of the Mas-related X2 (MRGPRX2) in 2006 marked a major step in elucidating non-IgE-mediated mast cell activation pathways. This receptor, selectively expressed on mast cells, responds to diverse ligands such as neuropeptides and drugs, leading to independent of FcεRI. Subsequent research highlighted MRGPRX2's role in drug-induced pseudo-allergic reactions, explaining to agents like neuromuscular blockers and opioids through direct mast cell stimulation. Advancing into the 2010s, single-cell sequencing technologies unveiled substantial heterogeneity in mast cell populations across tissues and states, revealing distinct transcriptional profiles and functional subtypes that influence their roles in immunity and . This approach demonstrated variations in related to production and receptor usage, challenging prior views of mast cells as uniform effectors. Therapeutically, the 2017 FDA approval of midostaurin, a multi-kinase inhibitor targeting mutant KIT, provided the first systemic treatment for advanced , significantly improving outcomes in patients with KIT D816V mutations by inhibiting aberrant mast cell proliferation.

Current Research Directions

Heterogeneity and Subtypes

Mast cells exhibit significant heterogeneity, with recent single-cell sequencing (scRNA-seq) studies revealing distinct transcriptional profiles that define varying numbers of subtypes (typically 2 to 5) in different tissues and diseases, primarily differentiated by tissue location and functional specialization. For instance, in the healthy colon, scRNA-seq has identified five transcriptionally distinct mast cell subsets (MC1-5), each showing layer-specific distribution across mucosal, submucosal, and muscular layers, with variations in expression of genes related to proliferation, , and immune modulation. These subtypes reflect adaptations to local microenvironments, such as enhanced activity in connective tissue-like mast cells versus higher production in mucosal variants. Mast cell plasticity allows these cells to undergo environmental , altering their in response to local signals. Exposure to IL-4 and IL-13, key type 2 cytokines, shifts mast cells toward a pro-allergic by upregulating genes for IgE-mediated responses, production (e.g., , CCL13), and tissue remodeling factors, while suppressing pro-inflammatory pathways. This plasticity is evident in allergic contexts, where cytokine-rich environments enhance and release, contributing to chronic . Recent 2020s research highlights the role of mast cell progenitors (MCp) in establishing this heterogeneity through tissue imprinting during maturation. of human + hematopoietic progenitors has identified MCp populations expressing specific cytokine receptors (e.g., KIT, IL-3R), which guide their migration and differentiation into tissue-adapted mast cells upon entering sites like the or gut. This imprinting process imprints location-specific transcriptional signatures, such as increased IL-4 responsiveness in mucosal tissues, enabling functional specialization. The recognition of mast cell heterogeneity has profound implications for in allergies and . In allergic diseases, subtype-specific responses to triggers inform targeted therapies, such as IL-4/IL-13 inhibitors (e.g., ) for pro-allergic phenotypes, allowing tailored interventions based on tissue profiling. For , clonal mast cell variations drive diverse symptoms, with precision approaches like KIT inhibitor selected via mutation and heterogeneity analysis to address individual organ involvement and risk. These strategies underscore the potential for biomarker-driven diagnostics to optimize outcomes in heterogeneous mast cell disorders.

Emerging Therapeutic Targets

Recent advances in mast cell-targeted therapies have focused on inhibiting key activation pathways to address disorders such as chronic urticaria and . (BTK) inhibitors like fenebrutinib and remibrutinib block FcεRI signaling downstream, preventing release and production from human mast cells and in patients with refractory to antihistamines; both received FDA approval in 2025 for . Spleen tyrosine kinase (Syk) inhibitors target early signaling events in mast cell activation, offering complementary suppression of in activation disorders. For non-IgE-mediated pseudo-allergic reactions, antagonists of the mas-related X2 (MRGPRX2) represent a promising class of therapeutics. MRGPRX2, expressed on skin mast cells, triggers in response to certain drugs and neuropeptides, contributing to adverse reactions like perioperative anaphylaxis. Small-molecule MRGPRX2 antagonists have been shown to inhibit agonist-induced calcium mobilization and β-hexosaminidase release from human mast cells in an IgE-independent manner, with subnanomolar potency in recent screens. These compounds hold therapeutic potential for conditions involving pseudo-allergies, such as chronic urticaria and inflammatory skin diseases, where MRGPRX2 drives mast cell hyperactivity. Research models have advanced the development of these therapies through improved preclinical platforms. Humanized mouse models, engrafted with human CD34+ hematopoietic stem cells, support the differentiation and tissue-specific engraftment of functional mast cells expressing MRGPRX2 and FcεRI, enabling studies of allergic responses and drug testing. (iPSC)-derived mast cells provide a renewable, patient-specific source for , recapitulating disease phenotypes like KIT-mutated mastocytosis and responding to allergens with degranulation and mediator release. In the 2020s, CRISPR/Cas9 editing has been employed to introduce or correct KIT D816V mutations in mast cell lines and iPSC models, facilitating precise investigation of neoplastic mast cell disorders and evaluation of targeted inhibitors. Emerging insights into the microbiome-mast cell axis underscore its therapeutic relevance in modulating mast cell function. Gut has been linked to heightened mast cell activation in systemic , with altered microbial profiles correlating to increased and symptom severity. Therapeutic strategies targeting this axis, such as or fecal transplantation, show promise in restoring microbial balance to suppress mast cell and production in preclinical models of allergic and inflammatory diseases.

Mast Cells in Other Organisms

Comparative Biology in Vertebrates

Mast cells are a conserved feature across all classes, from cyclostomes to mammals, where they function as key effectors in innate immunity and tissue homeostasis. These cells are characterized by metachromatic granules containing bioactive mediators, including , which is stored and released upon activation in most evolutionarily advanced and all higher vertebrates. The stem cell factor receptor KIT (CD117) is expressed on mast cells in , birds, and mammals, facilitating their development and survival through interactions with its ligand. In contrast, the high-affinity IgE receptor FcεRI, central to allergic responses in mammals, appears to be a later evolutionary acquisition, with FcεRI-like receptors identified in mast cells but lacking the IgE specificity due to the absence of IgE in non-mammalian vertebrates. Notable differences in mast cell biology emerge across lineages, particularly in granule composition and pathways. In , mast cells exhibit phenotypic heterogeneity with two primary subtypes: mast cells (CTMCs), which reside in submucosal and perivascular locations and contain large granules rich in , carboxypeptidase A, and chymase; and mucosal mast cells (MMCs), found in the gastrointestinal and respiratory mucosae, featuring smaller granules with tryptase-like proteases and increased responsiveness to T-cell-derived cytokines during parasitic infections. Fish mast cells, while sharing ultrastructural similarities such as electron-dense granules and the capacity for , lack IgE-dependent mechanisms but store and serotonin in their granules, enabling rapid inflammatory responses akin to those in higher s. These variations highlight adaptations to diverse environmental pressures, with subtypes reflecting specialized roles in mucosal versus defenses. Evolutionary studies reveal that mast cell orthologs in teleost fish, such as those expressing KIT-like receptors, contribute significantly to parasite defense by degranulating in response to helminth infections in the gut and gills, releasing mediators that recruit eosinophils and promote expulsion of invaders. This conserved role in antiparasitic immunity underscores the ancient origins of mast cells, likely emerging over 500 million years ago in early chordates to support vascular and inflammatory responses. In birds, mast cells similarly express KIT and release during inflammatory challenges, bridging piscine and mammalian functions. In , mast cell neoplasia holds particular relevance in companion animals, where tumors are the most common cutaneous in dogs, comprising 16-21% of skin neoplasms and often linked to KIT mutations that drive aggressive proliferation. In cats, mast cell tumors frequently affect the as the primary site and represent the second most common skin tumor, with variable influenced by histological grade and c-KIT alterations. These conditions parallel neoplastic disorders in other vertebrates but emphasize the clinical importance of mast cells in canine and feline , informing targeted therapies like inhibitors.

Presence in Invertebrates

Mast cell-like cells, characterized by their granular content and ability to degranulate in response to stimuli, have been identified in various invertebrate phyla, predating the evolution of adaptive immunity in vertebrates. These cells contribute to innate immune defenses through rapid release of mediators, including vasoactive amines such as histamine, facilitating responses to injury, pathogens, and parasites. Their presence underscores an ancient origin for such effector mechanisms, linked to primitive degranulation processes that enhance survival in diverse environments. In , such as , granular hemocytes serve as analogs to mast cells, exhibiting phagocytic activity and to release vasoactive substances. These hemocytes, abundant in circulation, contain cytoplasmic granules that discharge contents during immune challenges, contributing to and wound repair. For instance, in , hemocytes participate in and hemostatic functions akin to mast cell actions. Annelids, including earthworms like , possess coelomocytes that function in responses through granular and . These macrophage-like cells, originating from the coelomic lining, rapidly accumulate at injury sites, releasing vasoactive amines such as to promote clotting and tissue repair. has been detected in nervous systems and extracts, supporting its role in modulating inflammatory cascades during . Additionally, inflammatory responses involve potential mast cell analogs that participate in vasoactive substance-mediated feedback, though distinct from . In nematodes, coelomocytes exhibit mast cell-like functions, particularly in parasite encapsulation and innate defense. These variable-shaped cells, ranging from ovoid to stellate, engulf and encapsulate foreign invaders, forming multilayered barriers to isolate pathogens. In species like , coelomocytes perform and to contain bacterial or parasitic threats through engulfment and degradation, supporting innate immunity. This process is crucial for survival against intra-coelomic invaders, highlighting a conserved innate mechanism. Molecular parallels between and systems include G protein-coupled receptors (GPCRs) for sensing, akin to Mas-related GPCRs (MRGPRs) in mast cells. In C. elegans, over 150 -activated GPCRs, part of the rhodopsin family like MRGPRs, detect peptides to trigger cellular responses, including immune modulation. These receptors deorphanize signaling pathways that regulate aggregation, aerotaxis, and pathogen avoidance, suggesting evolutionary conservation of peptide-sensing for innate . The evolutionary origins of these mast cell-like cells trace back to non-vertebrate chordates, such as (e.g., Styela plicata and Botrylloides leachii), where granular immunocytes localize at body surfaces and release mediators upon environmental threats. Dating to approximately 500–680 million years ago, these cells likely represent precursors to mast cells, emphasizing innate as a pre-adaptive immune strategy.

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