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Embryology
Embryology
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1 - morula, 2 - blastula
1 - blastula, 2 - gastrula with blastopore; orange - ectoderm, red - endoderm

Embryology (from Greek ἔμβρυον, embryon, "the unborn, embryo"; and -λογία, -logia) is the branch of animal biology that studies the prenatal development of gametes (sex cells), fertilization, and development of embryos and fetuses. Embryology includes teratology, the study of congenital disorders that occur before birth.

Early embryology was proposed by Marcello Malpighi, and known as preformationism, the theory that organisms develop from pre-existing miniature versions of themselves. Aristotle proposed the theory that is now accepted, epigenesis. Epigenesis is the idea that organisms develop from seed or egg in a sequence of steps. Modern embryology developed from the work of Karl Ernst von Baer, though accurate observations had been made in Italy by anatomists such as Aldrovandi and Leonardo da Vinci in the Renaissance.[citation needed]

Comparative embryology

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Preformationism and epigenesis

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A tiny person (a homunculus) inside a sperm, as drawn by Nicolaas Hartsoeker in 1695

As recently as the 18th century, the prevailing notion in western human embryology was preformation: the idea that a sperm cell itself contains an embryo—a preformed, miniature infant, or homunculus—which simply becomes larger as it develops.

The competing explanation of embryonic development was epigenesis, originally proposed 2,000 years earlier by Aristotle. Much early embryology came from the work of the Italian anatomists Aldrovandi, Aranzio, Leonardo da Vinci, Marcello Malpighi, Gabriele Falloppio, Girolamo Cardano, Emilio Parisano, Fortunio Liceti, Stefano Lorenzini, Spallanzani, Enrico Sertoli, and Mauro Ruscóni. According to epigenesis, the form of an animal emerges gradually from a relatively formless egg. As microscopy improved during the 19th century, biologists could see that embryos took shape in a series of progressive steps, and epigenesis displaced preformation as the favored explanation among embryologists.

Cleavage

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Cleavage is the very beginning steps of a developing embryo. Cleavage refers to the many mitotic divisions that occur after the egg is fertilized by the sperm. The ways in which the cells divide is specific to certain types of animals and may have many forms.

Holoblastic

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Holoblastic cleavage is the complete division of cells. Holoblastic cleavage can be radial (see: Radial cleavage), spiral (see: Spiral cleavage), bilateral (see: Bilateral cleavage), or rotational (see: Rotational cleavage). In holoblastic cleavage, the entire egg will divide and become the embryo, whereas in meroblastic cleavage, some cells will become the embryo and others will be the yolk sac.

Meroblastic

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Meroblastic cleavage is the incomplete division of cells. The division furrow does not protrude into the yolky region as those cells impede membrane formation and this causes the incomplete separation of cells. Meroblastic cleavage can be bilateral (see: Bilateral cleavage), discoidal (see: Discoidal cleavage), or centrolecithal (see: Centrolecithal).

Basal phyla

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Animals that belong to the basal phyla have holoblastic radial cleavage which results in radial symmetry (see: Symmetry in biology). During cleavage, there is a central axis that all divisions rotate about. The basal phyla also has only one to two embryonic cell layers, compared to the three in bilateral animals (endoderm, mesoderm, and ectoderm).

Bilaterians

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In bilateral animals, cleavage can be either holoblastic or meroblastic depending on the species. During gastrulation, the blastula develops in one of two ways that divide the whole animal kingdom into two-halves (see: Embryological origins of the mouth and anus). If in the blastula, the first pore, or blastopore, becomes the mouth of the animal, it is a protostome; if the blastopore becomes the anus, then it is a deuterostome. The protostomes include most invertebrate animals, such as insects, worms and molluscs, while the deuterostomes include a few invertebrates such as the echinoderms (starfish and relatives) and all the vertebrates. In due course, the blastula changes into a more differentiated structure called the gastrula. Soon after the gastrula is formed, three distinct layers of cells (the germ layers) from which all the bodily organs and tissues then develop.

Germ layers

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  • The innermost layer, or endoderm, give rise to the digestive organs, the gills, lungs or swim bladder if present, and kidneys or nephrites.
  • The middle layer, or mesoderm, gives rise to the muscles, skeleton if any, and blood system.
  • The outer layer of cells, or ectoderm, gives rise to the nervous system, including the brain, and skin or carapace and hair, bristles, or scales.

Drosophila melanogaster (fruit fly)

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Drosophila have been used as a developmental model for many years. The studies that have been conducted have discovered many useful aspects of development that not only apply to fruit flies but other species as well.

Outlined below is the process that leads to cell and tissue differentiation.

  1. Maternal-effect genes help to define the anterior-posterior axis using Bicoid (gene) and Nanos (gene).
  2. Gap genes establish 3 broad segments of the embryo.
  3. Pair-rule genes define 7 segments of the embryo within the confines of the second broad segment that was defined by the gap genes.
  4. Segment-polarity genes define another 7 segments by dividing each of the pre-existing 7 segments into anterior and posterior halves using a gradient of Hedgehog and Wnt.
  5. Homeotic (Hox) genes use the 14 segments as pinpoints for specific types of cell differentiation and the histological developments that correspond to each cell type.

Humans

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Humans are bilateral animals that have holoblastic rotational cleavage. Humans are also deuterostomes. In regard to humans, the term embryo refers to the ball of dividing cells from the moment the zygote implants itself in the uterus wall until the end of the eighth week after conception. Beyond the eighth week after conception (tenth week of pregnancy), the developing human is then called a fetus.

Evolutionary embryology

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Evolutionary embryology is the expansion of comparative embryology by the ideas of Charles Darwin. Similarly to Karl Ernst von Baer's principles that explained why many species often appear similar to one another in early developmental stages, Darwin argued that the relationship between groups can be determined based upon common embryonic and larval structures.

Von Baer's principles

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  1. The general features appear earlier in development than do the specialized features.
  2. More specialized characters develop from the more general ones.
  3. The embryo of a given species never resembles the adult form of a lower one.
  4. The embryo of a given species does resemble the embryonic form of a lower one.[1]

Using Darwin's theory evolutionary embryologists have since been able to distinguish between homologous and analogous structures between varying species. Homologous structures are those that the similarities between them are derived from a common ancestor, such as the human arm and bat wings. Analogous structures are those that appear to be similar but have no common ancestral derivation.[1]

Origins of modern embryology

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Until the birth of modern embryology through observation of the mammalian ovum by Karl Ernst von Baer in 1827, there was no clear scientific understanding of embryology, although later discussions in this article show that some cultures had a fairly refined understanding of some of the principles. Only in the late 1950s when ultrasound was first used for uterine scanning, was the true developmental chronology of human fetus available. Karl Ernst von Baer along with Heinz Christian Pander, also proposed the germ layer theory of development which helped to explain how the embryo developed in progressive steps. Part of this explanation explored why embryos in many species often appear similar to one another in early developmental stages using his four principles.

Modern embryology research

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Embryology is central to evolutionary developmental biology ("evo-devo"), which studies the genetic control of the development process (e.g. morphogens), its link to cell signalling, its roles in certain diseases and mutations, and its links to stem cell research. Embryology is the key to Gestational Surrogacy, which is when the sperm of the intended father and egg of intended mother are fused in a lab forming an embryo. This embryo is then put into the surrogate who carries the child to term.

Medical embryology

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Medical embryology is used widely to detect abnormalities before birth. 2-5% of babies are born with an observable abnormality and medical embryology explores the different ways and stages that these abnormalities appear in.[1] Genetically derived abnormalities are referred to as malformations. When there are multiple malformations, this is considered a syndrome. When abnormalities appear due to outside contributors, these are disruptions. The outside contributors causing disruptions are known as teratogens. Common teratogens are alcohol, retinoic acid,[2] ionizing radiation or hyperthermic stress.

Vertebrate and invertebrate embryology

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Many principles of embryology apply to invertebrates as well as to vertebrates. Therefore, the study of invertebrate embryology has advanced the study of vertebrate embryology. However, there are many differences as well. For example, numerous invertebrate species release a larva before development is complete; at the end of the larval period, an animal for the first time comes to resemble an adult similar to its parent or parents. Although invertebrate embryology is similar in some ways for different invertebrate animals, there are also countless variations. For instance, while spiders proceed directly from egg to adult form, many insects develop through at least one larval stage. For decades, a number of so-called normal staging tables were produced for the embryology of particular species, mainly focussing on external developmental characters. As variation in developmental progress makes comparison among species difficult, a character-based Standard Event System was developed, which documents these differences and allows for phylogenetic comparisons among species.[3]

Birth of developmental biology

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After the 1950s, with the DNA helical structure being unraveled and the increasing knowledge in the field of molecular biology, developmental biology emerged as a field of study which attempts to correlate the genes with morphological change, and so tries to determine which genes are responsible for each morphological change that takes place in an embryo, and how these genes are regulated.

As of today, human embryology is taught as a cornerstone subject in medical schools, as well as in biology and zoology programs at both an undergraduate and graduate level.

History

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Ancient Egypt

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Knowledge of the placenta goes back at least to ancient Egypt, where it was viewed as the seat of the soul. There was an Egyptian official with the title Opener of the Kings Placenta. An Egyptian text from the time of Akhenaten said that a human originates from the egg that grows in women.[4]

Ancient Asia

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Various interpretations of embryology have existed in Asia throughout history.[5] Included in the ancient Indian tradition of Ayurveda is garbhasharir or the study of embryology, which refers to conceptions of embryology from antiquity.[6][7] Descriptions of the amniotic sac appear in the Bhagavad Gita, Bhagavata Purana,[8] and the Sushruta Samhita. One of the Upanishads known as the Garbhopanisaḍ states that the embryo is "like water in the first night, in seven nights it is like a bubble, at the end of half a month it becomes a ball. At the end of a month it is hardened, in two months the head is formed".[9] In Indian literature, the start of consciousness in an embryo is not clearly defined. Some scriptures state that it is active at conception, while others suggest that consciousness begins in the seventh to ninth month of fetal development. Many South Asian traditions, including some Tibetan traditions, believe that the fetus has conscious experiences towards the end of its development.[10]

The development of the human embryo is mentioned in the ancient Buddhist text of Garbhāvakrāntisūtra (1st-4th century CE). It mentions the human gestation period of 38 days. The text describes embryonic development in first three weeks as a liquid part of yogurt and the differentiation of body parts such as arms, leg, feet and head in the third month.[11][9]

Ancient Greece

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Pre-Socratic philosophers

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Many pre-Socratic philosophers are recorded as having opinions on different aspects of embryology, although there is some bias in the description of their views in later authors such as Aristotle. According to Empedocles (whose views are described by Plutarch in the 1st century AD), who lived in the 5th century BC, the embryo derives and receives its blood from four vessels in all; two arteries and two veins. He also held sinews as originating from equal mixtures of earth and air. He further said men begin to form within the first month and are finished within fifty days. Asclepiades agreed that men are formed within fifty days, but he believed that women took a full two months to be fully knit. One observation, variously attributed to either Anaxagoras of Clazomenae or Alcmaeon of Croton, says that the milk produced by mammals is analogous to the white of fowl egg. Diogenes of Apollonia said that a mass of flesh forms first, only then followed by the development of bone and nerves. Diogenes recognized that the placenta was a nutritional source for the growing fetus. He also said that the development of males took four months, but that the development of females took five months. He did not think the embryo was alive. Alcmaeon also made some contributions, and he is the first person reported to have practiced dissection. One idea, first stated by Parmenides, was that there was a connection between the right side of the body and the male embryo, and between the left side of the body and the female embryo. According to Democritus and Epicurus, the fetus is nourished at the mouth inside the mother and there are comparable teats that supply this nourishment within the mother's body to the fetus.[12] Discussion on various views regarding how long it takes for specific parts of the embryo to form appear in an anonymous document known as the Nutriment.

Ancient Greeks discussed whether only the male had a seed which developed into the embryo within the female womb, or both the male and the female each had a seed that made a contribution to the developing embryo. The difficulty that one-seed theorists confronted was to explain the maternal resemblance of the progeny. One issue that two-seed theorists confronted was why the female seed was needed if the male already had a seed. One common solution to this problem was to assert that the female seed was either inferior or inactive. Another question was the origin of the seed. The encephalomyelogenic theory stated that the seed originated from the brain or and/or bone marrow. Later came pangenesis, which asserted the seed was drawn from the whole body in order to explain the general resemblance in the body of the offspring. Later on hematogenous theory developed which asserted that the seed was drawn from the blood. A third question was how or in what form the progeny existed in the seed prior to developing into an embryo and a fetus. According to preformationists, the body of the progeny already existed in a pre-existing but undeveloped form in the seed. Three variants of preformationism were homoiomerous preformationism, anhomoiomerous preformationism, and homuncular preformationism. According to the first, the homoiomerous parts of the body (e.g. humors, bone) already exist pre-formed in the seed. The second held that it was the anhomoiomerous parts that were pre-formed. Finally, the third view held that the whole was already a unified organic thing. Preformationism was not the only view. According to epigenesists, parts of the embryo successively form after conception takes place.[13]

Hippocrates

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Some of the most well-known early ideas on embryology come from Hippocrates and the Hippocratic Corpus, where discussion on the embryo is usually given in the context of discussing obstetrics (pregnancy and childbirth). Some of the most relevant Hippocratic texts on embryology include the Regimen on Acute Diseases, On Semen, and On the Development of the Child. Hippocrates claimed that the development of the embryo is put into motion by fire and that nourishment comes from food and breath introduced into the mother. An outer layer of the embryo solidifies, and the fire within consumes humidity which makes way for development of bone and nerve. The fire in the innermost part becomes the belly and air channels are developed in order to route nourishment to it. The enclosed fire also helps form veins and allows for circulation. In this description, Hippocrates aims at describing the causes of development rather than describing what develops. Hippocrates also develops views similar to preformationism, where he claims that all parts of the embryo simultaneously develop. Hippocrates also believed that maternal blood nourishes the embryo. This blood flows and coagulates to help form the flesh of the fetus. This idea was derived from the observation that menstrual blood ceases during pregnancy, which Hippocrates took to imply that it was being redirected to fetal development. Hippocrates also claimed that the flesh differentiates into different organs of the body, and Hippocrates saw as analogous an experiment where a mixture of substances placed into water will differentiate into different layers. Comparing the seed to the embryo, Hippocrates further compared the stalk to the umbilical cord.[14]

Aristotle

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Some embryological discussion appears in the writings of Aristotle's predecessor Plato, especially in his Timaeus. One of his views were that the bone marrow acted as the seedbed, and that the soul itself was the seed out of which the embryo developed, though he did not explain how this development proceeded. Scholars also continue to debate the views he held on various other aspects of embryology.[13] However, a much more voluminous discussion on the subject comes from the writings of Aristotle, especially as appears in his On the Generation of Animals.[15] Some ideas related to embryology also appear in his History of Animals, On the Parts of Animals, On Respiration, and On the Motion of Animals. Means by which we know Aristotle studied embryology, and most likely his predecessors as well, was through studying developing embryos taken out from animals as well as aborted and miscarried human embryos. Aristotle believed that the female supplied the matter for the development of the embryo, formed from the menstrual blood whereas the semen that comes from the male shapes that matter. Aristotle's belief that both the male and female made a contribution to the actual fetus goes against some prior beliefs. According to Aeschylus and some Egyptian traditions, the fetus solely develops from the male contribution and that the female womb simply nourishes this growing fetus. On the other hand, the Melanesians held that the fetus is solely a product of the female contribution. Aristotle did not believe there were any external influences on the development of the embryo. Against Hippocrates, Aristotle believed that new parts of the body developed over time rather than all forming immediately and developing from then on. He also considered whether each new part derives from a previously formed part or develops independently of any previously formed part. On the basis that different parts of the body do not resemble each other, he decided in favor of the latter view. He also described development of fetal parts in terms of mechanical and automatic processes. In terms of the development of the embryo, he says it begins in a liquid-like state as the material secreted by the female combines with the semen of the male, and then the surface begins to solidify as it interacts with processes of heating and cooling. The first part of the body to differentiate is the heart, which Aristotle and many of his contemporaries believed was the location of reason and thinking. Aristotle claimed that vessels join to the uterus in order to supply nourishment to the developing fetus. Some of the most solid parts of the fetus cool and, as they lose moisture to heat, turn into nails, horns, hoofs, beaks, etc. Internal heat dries away moisture and forms sinews and bones and the skin results from drying of the flesh. Aristotle also describes the development of birds in eggs at length. He further described embryonic development in dolphins, some sharks, and many other animals. Aristotle singularly wrote more on embryology than any other pre-modern author, and his influence on the subsequent discussion on the subject for many centuries was immense, introducing into the subject forms of classification, a comparative method from various animals, discussion of the development of sexual characteristics, compared the development of the embryo to mechanistic processes, and so forth.[16]

Later Greek embryology

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Reportedly, some Stoics claimed that most parts of the body formed at once during embryological development. Some Epicureans claimed that the fetus is nourished by either the amniotic fluid or the blood, and that both male and female supply material to the development of the fetus. According to the writings of Tertullian, Herophilus in the 5th century BC described the ovaries and fallopian tubes (but not past what was already described by Aristotle) and also dissected some embryos. One advance Herophilus made, against the conceptions of other individuals such as Aristotle, was that the brain was the center of intellect rather than the heart. Though not a part of Greek tradition, in Job 10, the formation of the embryo is likened to the curdling of milk into cheese, as described by Aristotle. Whereas Needham sees this statement in Job as part of the Aristotelian tradition, others see it as evidence that the milk analogy predates the Aristotelian Greek tradition and originates in Jewish circles.[17] In addition, the Wisdom of Solomon (7:2) also has the embryo formed from menstrual blood. Soranus of Ephesus also wrote texts on embryology which went into use for a long time. Some rabbinic texts discuss the embryology of a female Greek writer named Cleopatra, a contemporary of Galen and Soranus, who was said to have claimed that the male fetus is complete in 41 days whereas the female fetus is complete in 81 days. Various other texts of less importance also appear and describe various aspects of embryology, though without making much progress from Aristotle. Plutarch has a chapter in one of his works titled "Whether was before, the hen or egg?" Discussion on embryological tradition also appears in many Neoplatonic traditions.[18]

Next to Aristotle, the most impactful and important Greek writer on biology was Galen of Pergamum, and his works were transmitted throughout the Middle Ages. Galen discusses his understanding of embryology in two of his texts, those being his On the Natural Faculties and his On the Formation of the Foetus.[19] There is an additional text spuriously attributed to Galen known as On the Question of whether the Embryo is an Animal. Galen described embryological development in four stages. In the first stage, the semen predominates. In the second stage, the embryo is filled with blood. In the third stage, the main outlines of the organs have developed but various other parts remain undeveloped. In the fourth stage, formation is complete and has reached a stage where we can call it a child. Galen described processes that played a role in furthering development of the embryo such as warming, drying, cooling, and combinations thereof. As this development plays out, the form of life of the embryo also moves from that like a plant to that of an animal (where the analogy between the root and umbilical cord is made). Galen claimed that the embryo forms from menstrual blood, by which his experimental analogy was that when you cut the vein of an animal and allow blood to flow out and into some mildly heated water, a sort of coagulation can be observed. He gave detailed descriptions of the position of the umbilical cord relative to other veins.[20]

Patristics

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The question of embryology is discussed among a number of early Christian writers, largely in terms of theological questions such as whether the fetus has value and/or when it begins to have value. (Although a number of Christian authors continued the classical discussions on the description of the development of the embryo, such as Jacob of Serugh.[21] Passing reference to the embryo also appears in the eighth hymn of Ephrem the Syrian's Paradise Hymns.[22]) Many patristic treatments of embryology continued in the stream of Greek tradition.[23] The earlier Greek and Roman view that it was not was reversed and all pre-natal infanticide was condemned. Tertullian held that the soul was present from the moment of conception. The Quinisext Council concluded that "we pay no attention to the subtle division as to whether the foetus is formed or unformed". In this time, then, the Roman practice of child exposure came to an end, where unwanted yet birthed children, usually females, were discarded by the parents to die.[24] Other more liberal traditions followed Augustine, who instead viewed that the animation of life began on the 40th day in males and the 80th day in females but not prior. Before the 40th day for men and 80th day for women, the embryo was referred to as the embryo informatus, and after this period was reached, it was referred to as the embryo formatus. The notion originating from the Greeks that the male embryo developed faster remained in various authors until it was experimentally disproven by Andreas Ottomar Goelicke in 1723.[25]

Various patristic literature from backgrounds ranging from Nestorian, Miaphysite and Chalcedonian discuss and choose between three different conceptions on the relation between the soul and the embryo. According to one view, the soul pre-exists and enters the embryo at the moment of conception (prohyparxis). According to a second view, the soul enters into existence at the moment of conception (synhyparxis). In a third view, the soul enters into the body after it has been formed (methyparxis). The first option was proposed by Origen, but was increasingly rejected after the fourth century. On the other hand, the other two options were equally accepted after this point. The second position appears to have been proposed as a response to Origen's notion of a pre-existing soul. After the sixth century, the second position was also increasingly seen as Origenist and so rejected on those grounds. The writings of Origen were condemned during the Second Origenist Crises in 553. Those defending prohyparxis usually appealed to the Platonic notion of an eternally moving soul. Those defending the second position also appealed to Plato but rejected his notion on the eternality of the soul. Finally, those appealing to the third position appealed both to Aristotle and scripture. Aristotelian notions included the progression of the development of the soul, from an initial plant-like soul, to a sensitive soul found in animals and allows for movement and perception, and finally the formation of a rational soul which can only be found in the fully-formed human. Furthermore, some scriptural texts were seen as implying the formation of the soul temporally after the formation of the body (namely Genesis 2:7; Exodus 21:22-23; Zachariah 12:1). In the De hominis opificio of Gregory of Nyssa, Aristotle's triparitate notion of the soul was accepted. Gregory also held that the rational soul was present at conception. Theodoret argued based on Genesis 2:7 and Exodus 21:22 that the embryo is only ensouled after the body is fully formed. Based on Exodus 21:22 and Zachariah 12:1, Philoxenus of Mabbug claimed that the soul was created in the body forty days after conception. In his De opificio mundi, the Christian philosopher John Philoponus claimed that the soul is formed after the body. Later still, the author Leontius held that the body and soul were created simultaneously, though it is also possible he held that the soul pre-existed the body.[26]

Some Miaphysites and Chalcedonians seemed to have been compelled into accepting synhyparxis in the case of Jesus because of their view that the incarnation of Christ resulted in both one hypostasis and one nature, whereas some Nestorians claimed that Christ, like us, must have had his soul formed after the formation of his body because, per Hebrews 4:15, Christ was like us in all ways but sin. (On the other hand, Leontinus dismissed the relevance of Hebrews 4:15 on the basis that Christ differed from us not only in sinfulness but also conception without semen, making synhyparxis another of Christ's supernatural feats.) They felt comfortable holding this view, under their belief that the human nature of Jesus was separate from the divine hypostasis. Some Nestorians still wondered, however, if the body united with the soul in the moment the soul was created or whether it came with it only later. The Syriac author Babai argued for the former on the basis that the latter was hardly better than adoptionism. Maximus the Confessor ridiculed the Aristotelian notion of the development of the soul on the basis that it would make humans parents of both plants and animals. He held to synhyparxis and regarded the other two positions both as incorrect extremes. After the 7th century, Chalcedonian discussion on embryology is slight and the few works that touch on the topic support synhyparxis. But debate among other groups remains lively, still divided on similar sectarian grounds. The patriarch Timothy I argued that the Word first united with the body, and only later with the soul. He cited John 1:1, claiming on its basis that the Word became flesh first, not a human being first. Then, Jacob of Edessa rejected prohyparxis because Origen had defended it and methyparxis because he believed that it made the soul ontologically inferior and as only being made for the body. Then, Moses Bar Kepha claimed, for Christological reasons as a Miaphysite, that only synhyparxis was acceptable. He claimed that Genesis 2:7 has no temporal sequence and that Exodus 21:22 regards the formation of the body and not the soul and so is not relevant. To argue against methyparxis, he reasoned that body and soul are both present at death and, because what is at the end must correspond to what is also at the beginning, conception must also have body and soul together.[26]

Embryology in Jewish tradition

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Many Jewish authors also discussed notions of embryology, especially as they appear in the Talmud. Much of the embryological data in the Talmud is part of discussions related to the impurity of the mother after childbirth. The embryo was described as the peri habbetten (fruit of the body) and it developed through various stages: (1) golem (formless and rolled-up) (2) shefir meruqqam (embroidered foetus) (3) ubbar (something carried) (4) walad (child) (5) walad shel qayama (viable child) (6) ben she-kallu khadashaw (child whose months have been completed).

Some mystical notions regarding embryology appear in the Sefer Yetzirah. The text in the Book of Job relating to the fetus forming by analogy to the curdling of milk into cheese was cited in the Babylonian Talmud and in even greater detail in the Midrash: "When the womb of the woman is full of retained blood which then comes forth to the area of her menstruation, by the will of the Lord comes a drop of white-matter which falls into it: at once the embryo is created. [This can be] compared to milk being put in a vessel: if you add to it some lab-ferment [drug or herb], it coagulates and stands still; if not, the milk remains liquid."[17] The Talmud sages held that there were two seeds that participated in the formation of the embryo, one from the male and one from the female, and that their relative proportions determine whether that develops into a male or a female.

In the Tractate Nidda, the mother was said to provide a "red-seed" which allows for the development of skin, flesh, hair, and the black part of the eye (pupil), whereas the father provides the "white-seed" which forms the bones, nerves, brain, and the white part of the eye. And finally, God himself was thought to provide the spirit and soul, facial expressions, capacity for hearing and vision, movement, comprehension, and intelligence. Not all strands of Jewish tradition accepted that both the male and female contributed parts to the formation of the fetus.

The 13th century medieval commentator Nachmanides, for example, rejected the female contribution. In Tractate Hullin in the Talmud, whether the organs of the child resemble more closely those of the mother or father is said to depend on which one contribute more matter to the embryo depending on the child. Rabbi Ishmael and other sages are said to have disagreed on one matter: they agreed that the male embryo developed on the 41st day, but disagreed on whether this was the case for the female embryo. Some believed that the female embryo was complete later, whereas others held that they were finished at the same time. The only ancient Jewish authors who associated abortion with homicide were Josephus and Philo of Alexandria in the 1st century. In the Talmud, a child is granted humanness at birth, while other rabbinical texts place it at the 13th postnatal day.[27]

Some Talmudic texts discuss magical influences on the development of the embryo, such as one text which claims that if one sleeps on a bed that is pointed to the north–south will have a male child. According to Nachmanides, a child born of a cold drop of semen will be foolish, one born from a warm drop of semen will be passionate and irascible, and one born from a semen drop of medium temperature will be clever and level-headed. Some Talmudic discussions follow from Hippocratic claims that a child born on the eighth month could not survive, whereas others follow Aristotle in claiming that they sometimes could survive. One text even says that survival is possible on the seventh month, but not the eighth. Talmudic embryology, in various aspects, follows Greek discourses especially from Hippocrates and Aristotle, but in other areas, makes novel statements on the subject.[17]

Judaism allows assisted reproduction, such as IVF embryo transfer and maternal surrogacy, when the spermatozoon and oocyte originate from the respective husband and wife.[28]

Embryology in the Islamic tradition

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Passing reference to embryological notions also appear in the Qur'an (22:5), where the development of the embryo proceeds in four stages from drop, to a clinging clot, to a partially developed stage, to a fully developed child.[29] The notion of clay turning into flesh is seen by some as analogous to a text by Theodoret that describes the same process.[30] The four stages of development in the Qur'an are similar to the four stages of embryological development as described by Galen. In the early 6th century, Sergius of Reshaina devoted himself to the translation of Greek medical texts into Syriac and became the most important figure in this process. Included in his translations were the relevant embryological texts of Galen. Anurshirvan founded a medical school in the southern Mesopotamian city of Gundeshapur, known as the Academy of Gondishapur, which also acted as a medium for the transmission, reception, and development of notions from Greek medicine. These factors helped the transmission of Greek notions on embryology, such as found in Galen, to enter into the Arabian milieu.[31] Very similar embryonic descriptions also appear in the Syriac Jacob of Serugh's letter to the Archdeacon Mar Julian.[21]

Embryological discussions also appear in the Islamic legal tradition.[32]

See also

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References

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Further reading

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Embryology is the branch of that studies the formation, growth, and development of the from fertilization through the establishment of major organ systems. It encompasses the development of embryos in humans and other organisms, providing insights into both medical and . In humans, this encompasses the prenatal period from the stage immediately after fertilization to about eight weeks post-fertilization (the end of the tenth week of ), when the embryo transitions to the fetal stage, marked by rapid , differentiation, and driven by genetic and environmental factors. The process begins with fertilization, where a penetrates the in the of the , forming a diploid that undergoes cleavage divisions to produce a multicellular morula and then a by day 5 post-fertilization. Implantation into the uterine wall occurs around days 6–10 post-fertilization (week 2). begins during week 3, where the three primary germ layers—, , and —form, laying the foundation for all tissues and organs. Subsequent weeks involve , including for the and somitogenesis for the musculoskeletal system, with critical cellular signaling pathways like Wnt, BMP, and FGF regulating these events. Embryology's insights extend to medical and evolutionary contexts, informing congenital anomaly prevention, assisted reproductive technologies such as in vitro fertilization (IVF), and understanding developmental disorders like arising from disrupted closure. Historically, the field advanced in the late with Wilhelm His's detailed reconstructions of embryos and Franklin Mall's establishment of the Carnegie Collection in 1887, which standardized staging via 23 still used today; modern progress includes the 1978 birth of the first IVF baby and genomic tools revealing gene regulatory networks in development.

Fundamentals

Definition and Scope

Embryology is the branch of biology that studies the prenatal development of organisms, focusing on the formation, growth, and differentiation of embryos from fertilization through key stages such as cleavage, gastrulation, and organogenesis. This field encompasses the molecular, cellular, and structural processes that transform a fertilized egg into a multicellular entity capable of independent life, applicable to both animals and humans. The term originates from the Greek words em bryon, meaning "young one in the womb," combined with -logia for "study of," reflecting its initial emphasis on mammalian development but later expanding to include non-mammalian species. The scope of embryology is limited to prenatal stages, beginning with formation and fertilization to produce a , progressing through embryonic and fetal development up to birth or hatching, while excluding postnatal growth and maturation. It integrates descriptive approaches, which document observable changes in form and structure, with experimental methods that investigate underlying mechanisms, such as and tissue interactions. Unlike broader , which includes postnatal processes like regeneration and , embryology prioritizes the initial establishment of body plans and organ systems. Embryology differs from morphology, which examines the static form and structure of organisms, by emphasizing dynamic developmental sequences rather than fixed anatomical features. Similarly, it contrasts with , the study of organismal functions and mechanisms in mature states, as embryology centers on the progressive differentiation and integration of cells into tissues and organs during early life stages. At its core, embryogenesis represents a coordinated series of cellular divisions, migrations, and transformations that generate the foundational architecture of the body, including the formation of germ layers that give rise to all major tissues.

Key Developmental Stages

Embryonic development begins with fertilization, the union of gametes to form a diploid . This process involves the penetrating the egg's outer layers, triggering the completion of in the oocyte and the fusion of haploid nuclei in syngamy, which restores the diploid number of chromosomes and activates the egg for development. Fertilization also initiates metabolic changes, such as the resumption of through the activation of mitosis-promoting factor (MPF), ensuring the zygote's readiness for subsequent divisions. Following fertilization, cleavage occurs as a series of rapid mitotic divisions that partition the zygote's into smaller cells called blastomeres, without a significant increase in overall mass. This stage eliminates the growth phases (G1 and G2) of the , relying initially on maternal mRNAs and proteins from the . Cleavage patterns vary: holoblastic cleavage, which is complete and divides the entire , is typical in amphibians and many , while meroblastic cleavage is partial, occurring only in the peripheral and seen in birds and reptiles due to their large reserves. By the end of cleavage, the forms a multicellular structure, such as the morula in mammals. Blastulation follows cleavage, resulting in the formation of the , a hollow sphere of blastomeres surrounding a fluid-filled cavity called the . In most animals, the blastula consists of undifferentiated cells that provide the foundation for further reorganization, while in mammals, the includes an that will give rise to the proper. This stage establishes the basic architecture for cell movements in later development. Gastrulation represents a pivotal reorganization where cells of the blastula migrate and rearrange to form the three primary germ layers: (outer layer), (middle layer), and (inner layer). These layers arise through processes like , involution, and , establishing the embryonic gut () and the primary body axes. The germ layers serve as precursors to all major tissues and organs, with contributing to the and , to muscles and circulatory structures, and to digestive and respiratory linings. Neurulation succeeds , primarily in chordates, where the thickens into a that folds to form the , the precursor to the including the and . This process is induced by signals from the underlying and involves somitogenesis, the segmentation of into somites that will form vertebrae, muscles, and . Concurrently, cells migrate to contribute to peripheral nerves, craniofacial structures, and pigment cells. Organogenesis then ensues as the germ layers differentiate into functional organ systems through inductive interactions and patterned cell proliferation. Major developments include the formation of the heart from mesoderm, limb buds from lateral plate mesoderm, and sensory organs from ectoderm. In vertebrates, this stage involves the elaboration of the circulatory, digestive, and urogenital systems, marking the transition from a simple embryo to one with recognizable body parts. Timeline variations in these stages reflect species-specific adaptations; for instance, in humans, the embryonic period encompassing cleavage through lasts approximately 8 weeks, with in week 3, completing by week 4, and major organ systems established by week 8, contrasting with shorter cycles in like fruit flies, where cleavage and occur within hours post-fertilization. In contrast, avian embryos exhibit extended due to dependency, spanning days before .

Historical Foundations

Ancient and Classical Contributions

In , medical papyri such as the , dating to approximately 1550 BCE, included descriptions related to , such as remedies for labor assistance and male production, reflecting early observational of pregnancy-related practices. These texts, alongside the from around 1825 BCE, documented gynecological conditions, , contraception, and practices, emphasizing the womb's central role in reproduction through medical treatments like pessaries and fumigations. In ancient Asian traditions, Chinese medical literature like the , compiled around 200 BCE, described fetal nourishment as dependent on the mother's and blood circulation, with the drawing sustenance from these vital energies for growth and development. Similarly, Indian Ayurvedic texts, particularly the (circa 600 BCE), outlined month-by-month embryonic development in the Garbha Vyakarana chapter, detailing how the transitions from a kalala (semisolid mass) in the first month to organ formation by the third, with full achieved by the seventh month through the integration of doshas. Pre-Socratic philosophers contributed conceptual frameworks to embryology, with (c. 490–430 BCE) proposing that the embryo arises from the mixture of four elemental roots—earth, water, air, and fire—governed by the forces of Love (attraction) and Strife (separation), analogous to cosmic embryogenesis where uniform blends form living tissues. (c. 460–370 BCE), in works attributed to the such as On the Nature of the Child, advanced the theory of , asserting that semen originates from all parts of the male body, carrying "seeds" or contributions from each organ to form the offspring, thus explaining inherited traits and congenital anomalies through parental bodily influences. Aristotle (384–322 BCE) laid foundational empirical groundwork through dissections of chick embryos at various incubation stages, as detailed in his Generation of Animals, observing the sequential appearance of the heart, blood vessels, and membranes from an initial bloody point, interpreting development as the teleological actualization of form from potential matter guided by the —material, formal, efficient, and final. This epigenesis-like view, where organs emerge progressively rather than preformed, contrasted with later theories and emphasized the embryo's purposive growth toward perfection. In the , anatomists Herophilus and (3rd century BCE) in extended these observations through human dissections, describing the 's vascular network—including connections from ovarian and uterine arteries—that supplies nourishment to the , while Herophilus noted the hollow structure of the and its ligaments, demystifying its role in . (c. 129–216 CE) advanced embryological understanding through extensive dissections of animal embryos, particularly chicks, describing developmental stages and systems, which influenced medieval and thought on generation.

Preformationism versus Epigenesis

The debate between preformationism and epigenesis dominated embryological thought from the 17th to the 19th century, representing a fundamental shift from viewing development as the unfolding of a pre-existing miniature organism to the gradual emergence of form from unorganized material. Preformationism posited that the embryo existed fully formed in miniature—termed a homunculus—within either the egg or sperm, awaiting only growth to maturity, while epigenesis argued for progressive differentiation and organization during development. This controversy arose amid advances in microscopy and philosophy, challenging earlier Aristotelian notions of development from a uniform material influenced by the environment. Preformationism gained prominence in the late 17th century through the work of Dutch microscopist Jan Swammerdam, who in his 1669 treatise Miraculum Naturae sive Utinam described insect metamorphosis as evidence of preformed structures unfolding without true novelty, suggesting a similar process in higher organisms. Philosopher Nicolas Malebranche extended this in the 1670s by proposing emboîtement, or encasement, where each embryo contains successively smaller embryos nested infinitely, resolving the origin of species through a single divine act of creation. This theory was bolstered by Antonie van Leeuwenhoek's 1677 microscopic observations of spermatozoa in human semen, which he interpreted as containing tiny, wriggling animalcules that carried the preformed offspring, thus supporting the idea of a complete organism within the male gamete. The doctrine split into ovism, championed by Regnier de Graaf, who in 1672 identified ovarian follicles as containing preformed embryos in the egg based on his studies of rabbit reproduction, and animalculism, advocated by Leeuwenhoek and others, which located the homunculus in the sperm as the active agent of generation. These views fueled heated disputes, with ovists emphasizing maternal contributions and animalculists paternal ones, yet both aligned with mechanistic philosophies that avoided unexplained creative forces in development. In contrast, epigenesis received philosophical backing from as early as 1637 in his correspondence and later works like La Description du Corps Humain (1648), where he described embryonic formation as a sequential process driven by mechanical motions of particles, without pre-existing forms, laying groundwork for a non-teleological view of generation. Empirical support came in 1759 from Caspar Friedrich Wolff's doctoral dissertation Theoria Generationis, which detailed observations of chick development, showing organs arising gradually through folding and differentiation of initially uniform tissues, such as the intestines forming from flat epithelial sheets into tubular structures, thus providing against preformation. The debate culminated in the early 19th century with von Baer's 1828 publication Über Entwickelungsgeschichte der Thiere, where meticulous comparative studies of mammalian and other vertebrate demonstrated progressive complexity from a simple blastoderm, empirically vindicating epigenesis and discrediting the nested homunculi of . Preformationism's appeal lay in its compatibility with theological doctrines of immutable , as the infinite encasement implied all organisms were created at once by , precluding transformation or and reinforcing fixed hierarchies in . Epigenesis, by positing development as an emergent process, facilitated evolutionary ideas by allowing for variability and through environmental influences on forming structures, paving the way for later theories of descent with modification.

Comparative Embryology

Cleavage and Early Division Patterns

Cleavage represents the initial series of mitotic divisions following fertilization, transforming the into a multicellular structure without significant growth in overall size. These divisions partition the egg's into progressively smaller blastomeres, establishing the foundation for subsequent embryonic development. The pattern and completeness of cleavage are primarily determined by the amount and distribution of within the egg, which influences mechanics and . Yolk, a nutrient-rich substance, inhibits and slows division rates in regions of high concentration, leading to distinct cleavage types based on . Isolecithal eggs, with sparse and uniformly distributed , undergo complete holoblastic cleavage, as seen in sea urchins and mammals. In contrast, telolecithal eggs feature concentrated at the vegetal pole, resulting in unequal or partial divisions, while centrolecithal eggs have centrally located that restricts cleavage to the periphery. Mesolecithal eggs, with moderate biased toward one pole, exhibit holoblastic but unequal cleavage, such as in amphibians. Holoblastic cleavage involves the complete division of the entire and is characteristic of eggs with little to moderate . It produces equal-sized blastomeres in isolecithal eggs, fostering symmetric arrangements. Radial holoblastic cleavage, observed in echinoderms like sea urchins, features blastomeres stacked in radial tiers around the animal-vegetal axis, culminating in a hollow blastula after approximately 128 cells. Spiral holoblastic cleavage, common in annelids and mollusks, twists blastomeres in a clockwise or counterclockwise spiral, with micromeres forming at the animal pole. In mammals, cleavage is rotational and holoblastic, with the first two divisions occurring in orthogonal planes, leading to a compacted morula stage. Amphibian eggs, being mesolecithal and telolecithal, display holoblastic cleavage that is unequal due to yolk-rich at the vegetal pole, where divisions proceed more slowly and produce larger blastomeres compared to the animal pole. This results in a multilayered blastula with a fluid-filled cavity forming between tiers of cells. Meroblastic cleavage, occurring in eggs with substantial , is incomplete and confined to the yolk-poor regions. Discoidal meroblastic cleavage in telolecithal eggs of birds and reptiles limits divisions to a disc-shaped area at the animal pole, forming a blastoderm atop the uncleaved yolk mass without penetrating the yolk. Superficial meroblastic cleavage in centrolecithal eggs of involves syncytial divisions at the egg's periphery, surrounding the central , which later cellularize to form a blastoderm. The culmination of cleavage often yields a blastula stage, a fluid-filled of cells. In mammals, the morula—a solid ball of 16 to 32 blastomeres—undergoes to form the , featuring an (future embryo) and surrounding layer enclosing the . This transition highlights the adaptive variations in early division patterns across taxa, driven by constraints.

Germ Layers and Gastrulation

Gastrulation represents a critical phase in embryonic development, transforming the blastula—a hollow of cells resulting from cleavage—into a multilayered gastrula that establishes the foundational . This process involves coordinated cellular movements that reorganize the embryo into three primary germ layers: , , and . These layers arise through morphogenetic processes such as , where cells fold inward to form an internal cavity; involution, in which cells roll over the edge of an opening like the blastopore; epiboly, the thinning and spreading of the outer cell sheet; and the formation of the , a primitive gut tube lined by that serves as the precursor to the digestive tract. The forms the outermost layer, destined to give rise to the and its appendages, as well as the , including the and derivatives. emerges as the middle layer between and , contributing to muscles, bones, connective tissues, and the , including the heart and blood vessels. The constitutes the innermost layer, originating the epithelial lining of the gut and associated glands such as the liver and . These fates are established during as cells ingress or migrate to specific positions, with the formation marking the internalization of precursors. Comparatively, gastrulation exhibits variations linked to developmental modes: deuterostomes typically display regulative development, where early embryonic cells remain totipotent and can compensate for perturbations, allowing flexible formation; in contrast, protostomes often follow mosaic development, with cell fates predetermined early, resulting in more rigid patterning during . play a high-level role in this context by providing positional cues that pattern structures within the germ layers along the anterior-posterior axis, ensuring organized differentiation across , , and .

Embryonic Development in Basal Phyla

Basal phyla, including Porifera, , , and , represent early-diverging metazoan lineages, with Porifera positioned as the earliest branch according to recent phylogenomic analyses, followed by , , and ; these groups exhibit structural simplicity, radial or biradial symmetry, and the absence of a distinct layer. These patterns highlight primitive mechanisms, such as holoblastic cleavage and straightforward , that form diploblastic or less organized body plans without the triploblastic complexity seen in more derived groups. In Porifera (sponges), embryonic development occurs internally within the mesohyl, leading to free-swimming larvae adapted for dispersal. Calcinean sponges produce the amphiblastula larva, a hollow sphere comprising anterior flagellated micromeres that will become choanocytes and posterior non-ciliated macromeres destined for pinacocytes, with additional cruciform cells and maternal remnants inside. This larva lacks true tissues, reflecting the asconoid or syconoid body plan of adults, and undergoes direct metamorphosis upon settlement, where micromeres differentiate internally to form the osculum without organogenesis. Gene expression patterns, such as posterior Wnt and TGF-β signaling, establish basic polarity but no complex axes. Cnidarians exhibit holoblastic, often synchronous cleavage that forms a coeloblastula, followed by primarily through to yield a with rudimentary and layers. In like , early cleavages are equal and unilateral, creating a by the 8- to 16-cell stage; involves apical constriction of bottle cells at the oral pole, deepening the via and blastopore involution, ultimately forming a ciliated, sausage-shaped competent for settlement. This diploblastic swims aborally and metamorphoses into a polyp, with compartmentalization aiding gut formation, though no develops. Variations include in some anthozoans, but predominates, underscoring the phylum's radial symmetry and simplicity. Ctenophores (comb jellies) undergo stereotypic holoblastic cleavage regulated by a cleavage clock, with divisions every 15-20 minutes establishing the oral-aboral axis by the first cleavage. Early divisions produce end (E) and middle (M) blastomeres; by the fourth cleavage, micromeres and macromeres differentiate, where E-lineage micromeres autonomously form comb plate cilia by 9 hours post-fertilization, while M-lineage micromeres require inductive signals for similar fates, and macromeres contribute to oral structures or photocytes. proceeds via around 3-4 hours, yielding a biradially symmetric without . Although previously proposed as the to all other animals in some molecular analyses, recent 2025 phylogenomic studies position after Porifera as an early-diverging lineage. Placozoans display the simplest metazoan development, with total, equal cleavage up to 128 cells or more, occurring within a maternal brood chamber formed by epithelial lifting. involves straightforward , establishing a two-layered of upper and lower epithelia surrounding a fiber cell , without distinct organs, nerves, or axes beyond basic polarity. Embryos are released after maternal degeneration under high-density, warm conditions (≥23°C), developing into dorsoventrally organized adults via asexual fission or rare sexual means, reflecting their early-diverging eumetazoan status post-Porifera and divergence. This minimalism, with only four cell types and rudimentary germ layers, underscores placozoans' primitive developmental toolkit.

Embryonic Development in Bilaterians

Bilaterian animals, characterized by their bilateral , exhibit sophisticated embryonic development that builds upon simpler patterns seen in basal phyla, such as cnidarians, by incorporating advanced features like true and segmentation. This development typically involves cleavage, , and , leading to the formation of a triploblastic with , , and germ layers. Unlike radial or irregular cleavage in non-bilaterians, bilaterian embryos often display determinate or indeterminate cleavage patterns that reflect their or lineages. Protostomes, including annelids and mollusks, undergo spiral cleavage, where early cell divisions produce a spiral of blastomeres, resulting in a determinate fate for each cell. This is followed by , a formation process in which the arises from splitting of the mesodermal mass during . For example, in annelids, embryonic development culminates in a , a free-swimming stage featuring a ciliated band for locomotion and feeding, which later metamorphoses into segmented juveniles. In contrast, deuterostomes, such as echinoderms and chordates, display radial indeterminate cleavage, allowing early blastomeres to retain totipotency and enabling regulative development. Their forms via enterocoely, where mesodermal pouches evaginate from the during . embryos, for instance, develop into a dipleurula-like with bilateral that undergoes dramatic reorganization to achieve radial adult , highlighting deuterostome developmental plasticity. Arthropods, as protostomes, feature superficial cleavage in their large, yolk-rich eggs, where divisions occur in a syncytial blastoderm without complete cell separation. Segmentation emerges through the periodic expression of genes like engrailed along the anterior-posterior axis, establishing parasegments that define body regions. This high-level patterning mechanism underscores the evolutionary conservation of segmentation in bilaterians. Chordates, a clade, develop characteristic embryonic structures including the , a mesodermal rod that provides axial support and induces formation, and pharyngeal slits, transient endodermal outpocketings that contribute to gill or development. These features are evident across embryos, from lancelets to vertebrates, reflecting shared developmental ancestry. Common to all bilaterians are the formation of a true coelom as a fluid-filled body cavity lined by mesoderm, which facilitates organ independence and movement, and the dorsal positioning of the neural tube, derived from ectodermal thickening and invagination during neurulation. These traits distinguish bilaterian embryology from basal forms and enable complex body plans.

Evolutionary Perspectives

Von Baer's Laws of Development

Karl Ernst von Baer, a Baltic German biologist, formulated his laws of development in 1828 while working at the University of Königsberg, based on extensive microscopic observations of embryos from various species, including the discovery of the mammalian ovum in dogs and detailed studies of chick development. These observations revealed that embryonic development proceeds through progressive differentiation rather than preformed structures, providing an empirical foundation for epigenesis over preformationism. Von Baer's work in Über Entwickelungsgeschichte der Thiere critiqued preformationist ideas, which posited that organisms develop from miniature pre-existing forms, by demonstrating that embryos arise from unorganized material and gradually acquire complexity through layered formation, such as the ectoderm and endoderm in early chick stages. Von Baer's states that the more general characters of a large group of animals appear earlier in the than the more special characters, meaning embryos initially exhibit broad features shared across taxa before species-specific traits emerge. The second law elaborates that from the most general forms, the less general are developed, and so on, until finally the most special arise, illustrating a hierarchical progression from shared ancestral-like forms to unique adult morphologies, as seen in the early similarity of and chick embryos diverging into distinct structures. The third law asserts that every embryo of a given animal form, instead of passing through the other forms, rather becomes separated from them, emphasizing branching divergence rather than linear progression through ancestral adult stages. Finally, the fourth law clarifies that fundamentally, the of a higher form never resembles any other form, but only its embryo, underscoring that similarities are confined to embryonic stages across related groups, not to adult forms of lower taxa. These laws provided a descriptive framework for comparative embryology, directly challenging preformationism by showing that development unfolds epigenetically from a generalized starting point, as evidenced by von Baer's findings that early mammalian embryos lack preformed organ rudiments and instead form them sequentially. In modern contexts, von Baer's principles are validated by the conserved early embryonic stages in s, such as the pharyngula stage where diverse species exhibit similar body plans before divergence, aligning with the hourglass model of development where early and late stages vary more than the mid-embryonic bottleneck. This conservation supports the idea that general features precede specialization across taxa, as observed in comparative studies of , , and mammalian embryos.

Evolutionary Developmental Biology

Evolutionary developmental biology, or evo-devo, integrates principles of embryology and to elucidate how changes in developmental processes generate morphological diversity across species. It examines the genetic and cellular mechanisms underlying formation, emphasizing that often acts by modifying conserved developmental pathways rather than inventing entirely new ones. Von Baer's laws of development, which describe the progressive divergence of embryos from a general to a specific form, served as early precursors by highlighting shared embryonic stages among related taxa. The field traces its origins to the , when proposed the biogenetic law in 1866, positing that recapitulates phylogeny, meaning embryos pass through stages resembling ancestral adult forms. This idea of was further developed by , who applied it to vertebrate evolution, suggesting that developmental sequences reflect phylogenetic history and that accelerations or delays in growth could drive morphological innovation. Although the strict was later critiqued for oversimplification, it laid foundational concepts for linking development to evolution. Evo-devo experienced a modern revival in the 1980s with the discovery of homeobox genes, particularly Hox clusters, which are conserved regulatory genes that specify segmental identity along the anterior-posterior axis in diverse animals, from insects to vertebrates. Central to evo-devo are concepts like and heterotopy, which describe evolutionary shifts in developmental timing and spatial patterning, respectively. Heterochrony involves changes in the onset, rate, or duration of developmental events, such as paedomorphosis where juvenile traits are retained into adulthood, leading to novel adult morphologies. Heterotopy refers to alterations in the position or orientation of structures during development, enabling innovations like the repositioning of limbs relative to the body axis. clusters exemplify these mechanisms by controlling organization through spatially restricted expression; for instance, collinear Hox activation patterns dictate regional identities in embryos. Illustrative examples include the evolution of vertebrate limbs from fish fins, where modifications in Sonic hedgehog (Shh) signaling expanded the zone of mesenchymal proliferation, promoting digit-like structures and autopodal elaboration. In arthropods, segmentation variations arise from divergent deployment of pair-rule and segment polarity genes, such as engrailed and wingless, resulting in diverse tagmosis patterns across taxa like and crustaceans. These cases demonstrate how subtle regulatory tweaks in shared genetic toolkits generate phylum-specific diversity. Developmental pathways impose constraints on evolution through canalization, the buffering of phenotypes against genetic and environmental perturbations, which stabilizes conserved body plans at levels while limiting radical innovations. For example, the modular architecture of Hox-regulated segments canalizes axial organization, explaining the persistence of bilaterian blueprints despite millions of years of divergence. Recent advances, including /Cas9 editing, have enabled precise testing of these constraints; post-2020 studies have used to disrupt evo-devo genes like Hox or Shh homologs, revealing how developmental robustness influences adaptive potential under environmental stress. In eco-evo-devo contexts, such experiments highlight roles in climate adaptation, where heterochronic shifts in , driven by temperature-sensitive regulatory networks, facilitate resilience in changing habitats.

Modern Advances

Molecular and Cellular Mechanisms

In modern embryology, molecular and cellular mechanisms orchestrate the precise patterning and differentiation of embryonic structures through intricate genetic and biochemical interactions. These processes begin with the establishment of body axes and progress to cell fate specification, involving regulatory networks, signaling cascades, adhesion molecules, , and epigenetic modifications. Such mechanisms ensure the transition from a totipotent to organized tissues, with germ layers serving as primary sites where these molecular actions unfold to generate , , and derivatives. Gene regulatory networks (GRNs) form the foundational framework for embryonic patterning, where genes deposited in the initiate axis formation. In , the bicoid gene exemplifies this, as its mRNA localizes to the anterior pole, producing a protein that specifies anterior structures along the anterior-posterior axis by activating downstream gap genes like hunchback in a concentration-dependent manner. This model, first elucidated through genetic screens, demonstrates how threshold-dependent transcription factors interpret positional information to drive segmental identity. Similar networks operate in vertebrates, where maternal factors such as VegT in establish dorsoventral polarity by regulating nodal signaling. Signaling pathways, including Wnt, BMP, and FGF, mediate inductive interactions critical for axis formation and tissue specification. Wnt signaling promotes anterior-posterior patterning in vertebrates by stabilizing β-catenin to activate target genes like brachyury in the , while its inhibition dorsally specifies the Spemann organizer. BMP gradients ventralize the embryo by repressing neural fate in , countered by antagonists like chordin from the organizer to induce dorsal structures. FGF pathways, often integrated with BMP and Wnt, drive mesoderm induction and movements, as seen in where FGF signaling maintains primitive streak progenitors. These pathways exhibit evolutionary conservation and functional redundancy, ensuring robust axis establishment across species. Cell adhesion and migration are governed by , which facilitate the dynamic rearrangements during . E-cadherin and N-cadherin mediate calcium-dependent homophilic interactions that maintain tissue integrity while allowing convergent extension movements, where cells intercalate to elongate the body axis in amphibians and . In , regulated cadherin expression enables bottle cells to ingress and mesendoderm to migrate, with downregulation of C-cadherin promoting epithelial-to-mesenchymal transition. These adhesion dynamics ensure proper without disrupting cellular cohesion. Apoptosis plays a pivotal role in sculpting embryonic structures by eliminating superfluous cells, particularly in digit formation where cell death separates digits in limbs. in the , triggered around embryonic day 12 in mice, involves activation and is essential for free digit separation, with defects leading to . BMP signaling directly induces this by upregulating pro-apoptotic genes like Msx2 in the zones, while FGF maintains chondrogenic survival in digit rays. This spatially restricted cell death highlights as a key mechanism for tissue morphogenesis. Epigenetic modifications, such as and histone modifications, maintain pluripotency by repressing differentiation genes in embryonic stem cells. Bivalent domains marked by (active) and (repressive) poise pluripotency factors like Oct4 for activation, while global DNA hypomethylation in the facilitates totipotency. acetyltransferases like p300 promote open at pluripotency loci, and disruptions in these marks, such as aberrant H3K9 methylation, impair self-renewal. These mechanisms ensure stable cell fate during early lineage commitment. Recent advances using single-cell sequencing (scRNA-seq) have refined our understanding of zygotic (ZGA), revealing its timing and heterogeneity. In humans, scRNA-seq demonstrates ZGA at the one-cell stage with minor waves, contrasting earlier views of major at the eight-cell stage, and highlights paternal contributions in androgenetic embryos. In , EU-labeled nascent sequencing post-2020 identified ZGA bursts at 2.5 and 4 hours post-fertilization, with maternal-zygotic transitions varying by cell type. These insights underscore ZGA as a dynamic, multi-phasic process critical for embryonic viability.

Techniques in Embryological Research

Classical techniques in embryological research laid the foundation for understanding embryonic induction and . Vital , pioneered by Walter Vogt in the 1920s, involved applying non-toxic dyes to specific regions of embryos to trace cell lineages and migration patterns during , enabling the creation of early fate maps without disrupting development. Transplantation experiments, notably those by and Hilde Mangold in 1924, demonstrated the inductive capacity of the dorsal blastopore lip—termed the "organizer"—when grafted into a host embryo, inducing a secondary axis and revealing mechanisms of embryonic patterning. These methods, combining for visualization and surgical manipulation, established key principles of embryonic and influenced subsequent studies on developmental signaling. Advancements in have enabled real-time observation of dynamic embryonic processes. , developed in the 1980s and refined for biological imaging, uses to produce high-resolution optical sections, minimizing out-of-focus light and allowing three-dimensional reconstruction of structures like formation in living embryos. Live-cell imaging techniques, often integrated with systems, facilitate tracking of cellular movements and over time, such as during , by incorporating fluorescent reporters that highlight specific proteins or organelles without . These approaches have transformed embryology by providing quantitative data on spatiotemporal dynamics, surpassing the limitations of fixed-sample . Molecular tools have revolutionized the study of gene function in embryos. (ISH), introduced in the 1980s for detecting transcripts, localizes patterns spatially within intact embryos, such as mapping during vertebrate segmentation, offering insights into regulatory networks. The CRISPR-Cas9 system, adapted from bacterial defense mechanisms and first demonstrated for in 2012, enables precise knockouts and modifications in embryonic cells, for instance, disrupting developmental genes like those involved in limb formation to elucidate causal roles. Applications since 2013 have included multiplex editing to study gene interactions, accelerating the identification of pathways in early development. Culture systems now permit ex vivo recapitulation of embryonic morphogenesis. Organoids, three-dimensional structures derived from stem cells, self-organize to mimic organ development, as seen in intestinal organoids that replicate villus formation and signaling gradients observed . Ex vivo embryo models, such as blastoids generated from pluripotent stem cells since 2018, simulate pre-implantation stages including and trophectoderm differentiation, providing platforms for studying implantation without relying on natural embryos. These systems enhance experimental control and scalability for high-throughput analysis of developmental perturbations. Omics approaches integrate high-throughput data to profile embryonic changes. Transcriptomics, via RNA sequencing, captures genome-wide expression dynamics, revealing temporal waves of activation during zebrafish somitogenesis that coordinate segmentation clocks. complements this by quantifying protein abundance and modifications, identifying post-translational regulators of timing in embryos, where discrepancies between mRNA and protein levels highlight regulatory layers. Multi-omics integration since the 2010s has mapped developmental trajectories, such as in pre-implantation stages, underscoring the role of epigenetic modifiers in lineage commitment. Ethical considerations have driven a toward human induced pluripotent stem cells (iPSCs) in embryological research. Following Shinya Yamanaka's 2006 demonstration of reprogramming adult fibroblasts into pluripotent cells using four transcription factors, iPSCs emerged as an alternative to embryonic stem cells, bypassing the destruction of embryos and enabling patient-specific models for developmental studies. This transition, recognized by Yamanaka's 2012 , has reduced reliance on animal models and addressed moral concerns over embryo use, fostering ethical progress in investigating -specific processes like . Recent updates, including the International Society for Stem Cell Research (ISSCR) guidelines revised in 2025, extend oversight to stem cell-based embryo models (SCBEMs), recommending enhanced review processes and prohibiting their use to initiate pregnancies to balance scientific advancement with ethical safeguards.

Model Organisms in Study

Model organisms play a crucial role in embryological research by providing experimentally tractable systems to elucidate conserved developmental mechanisms across species. These organisms are selected for attributes such as short generation times, genetic accessibility, and transparency, enabling detailed observation of embryonic processes. Seminal studies using these models have uncovered key principles of , , and , informing broader evolutionary and medical insights. Drosophila melanogaster, the fruit fly, is a foundational model in due to its short generation time of about 10 days and sophisticated genetic tools, including for mapping mutations. Its embryo develops externally and synchronously in large cohorts, facilitating of developmental mutants. A landmark contribution came from systematic screens identifying genes controlling segmentation, such as the maternal effect genes and gap genes that establish anterior-posterior polarity and segment number through hierarchical cascades. This work revealed the segmentation cascade, where maternal gradients initiate zygotic leading to periodic body segments, earning Christiane Nüsslein-Volhard and Eric Wieschaus the 1995 in or . Caenorhabditis elegans, a worm, offers unparalleled advantages for studying and owing to its transparent body, invariant developmental pattern, and complete mapping of its 959 somatic cells from to adult. Embryogenesis occurs rapidly over 12-14 hours at 20°C, allowing real-time imaging of every and migration. John Sulston's tracing of the embryonic demonstrated that development follows a fixed stereotypic path, with () eliminating 131 cells to sculpt tissues, providing the first full description of metazoan pathways. This invariant lineage has enabled precise genetic dissection of cell fate decisions, including the roles of Wnt signaling in asymmetry. The (Danio rerio) serves as a premier model for embryology, benefiting from , transparent embryos, and rapid completing major organ formation in 48-72 hours. Its large clutch sizes (hundreds per female) support genetic and chemical screens, while optical clarity permits live imaging of cellular dynamics. Key contributions include insights into fin regeneration, where blastema formation mirrors embryonic limb development, involving and progenitor proliferation regulated by FGF and Wnt pathways; this has established as a leader in studying regeneration mechanisms. Xenopus laevis, the , is valued for its large, pigmented eggs amenable to and microsurgery, facilitating studies of early development and nuclear reprogramming. Embryos develop externally over 2-3 days, allowing easy access for and transplantation. John Gurdon's 1962 experiments demonstrated that differentiated intestinal cell nuclei could be reprogrammed by enucleated eggs to support full development into fertile adults, proving genomic equivalence and paving the way for cloning technologies like . These findings underscored the egg's cytoplasmic factors in resetting epigenetic states during embryogenesis. The (Mus musculus) is the primary mammalian model for embryology, sharing 85-90% genetic homology with humans and enabling targeted manipulations to mimic states. Its 19-21 day allows timed studies of implantation to birth, with embryonic stem (ES) cell for precise interventions. Seminal work by , , and developed in ES cells to create knockout mice, disrupting specific to reveal their roles in development; for instance, knockouts have dissected vertebral patterning, while Shh knockouts illustrate defects, directly linking mutations to congenital anomalies. This approach, recognized by the 2007 , has generated over 10,000 knockout lines for . Emerging models are expanding embryological toolkits beyond traditional species. Organoids, three-dimensional stem cell-derived structures, recapitulate organ-specific development and interactions, such as gastrulation-like processes in blastoids or organoids modeling implantation post-2020. These systems bridge gaps in studying embryogenesis ethically, revealing gradients and tissue without animal use. Recent 2025 advances include programmable embryoids engineered from stem cells using methods to mimic the first days of embryonic development, enabling precise control over spatial architecture and lineage specification in models. The axolotl (Ambystoma mexicanum), a , has gained traction for regeneration studies due to its neotenic traits and ability to regrow limbs, , and organs throughout life, with embryos accessible for genetic tools like post-2020. Its large eggs and slow development ( at 2-3 weeks) enable detailed formation analysis, highlighting blastemal progenitors akin to embryonic .

Applications and Implications

Medical Embryology and Congenital Anomalies

Medical embryology examines the application of principles to prenatal growth, emphasizing how disruptions during embryogenesis lead to congenital anomalies, which affect approximately 6% of newborns worldwide. These anomalies arise from errors in , migration, or tissue interaction, often traceable to the three primary germ layers—ectoderm, , and —that give rise to all major organ systems, where defects in any layer can manifest as specific malformations. Understanding these processes is crucial for identifying risk factors and improving clinical outcomes in pediatric care. The human embryonic period spans the first eight weeks post-fertilization, during which major organ formation, or , occurs rapidly. In weeks 1-2, the fertilized ovum implants and forms the bilaminar disc, establishing foundational structures like the amniotic cavity and . By weeks 3-5, produces the trilaminar disc, and key systems emerge: the begins forming from , the heart tube loops and starts beating around day 22, and limb buds appear by week 4. Weeks 6-8 involve further differentiation, with organ rudiments maturing—eyes, ears, and digits becoming evident—while the reaches about 3 cm in length. Following this, the fetal period from week 9 to birth focuses on growth, refinement, and functional maturation of these organs, with less risk of major structural anomalies but potential for functional deficits. Teratology, the study of abnormal development, classifies congenital anomalies by etiology: genetic (e.g., single-gene mutations or chromosomal aberrations), environmental (teratogen exposure), or multifactorial (interactions between genetic susceptibility and environmental triggers). Genetic causes account for about 10-20% of cases, often involving disruptions in signaling pathways like those in the Sonic hedgehog or Wnt families. Environmental teratogens, such as infections or chemicals, disrupt during sensitive windows, while multifactorial anomalies, which comprise the majority (approximately 50-80%) of defects, result from polygenic inheritance combined with exposures like maternal or . A seminal example is the tragedy of the late 1950s to early 1960s, where the sedative, prescribed for , caused and other limb reductions in over 10,000 infants by interfering with and limb bud outgrowth during weeks 4-6 of gestation. This event prompted stricter drug regulations and highlighted the placenta's role in teratogen transmission. Among common anomalies, neural tube defects (NTDs) like arise from failed primary , where the neural folds fail to fuse by week 4, leading to incomplete closure of the and . This results in myelomeningocele, exposing neural tissue and causing , bladder dysfunction, and in affected individuals, with as a key modifiable risk. Congenital heart malformations, the most frequent birth defects (affecting 1% of live births), often stem from septation errors during weeks 4-7, such as incomplete partitioning of the atria or ventricles by the and muscular septa. For instance, ventricular septal defects occur when the membranous septum fails to form, allowing oxygenated and deoxygenated blood to mix, potentially requiring surgical correction. Prenatal diagnostics enable early detection of these anomalies through non-invasive and invasive methods. , performed routinely from week 8 onward, visualizes structural issues like NTDs (via the "lemon" sign of cranial defects) or heart septation flaws, with high sensitivity for major anomalies by the second trimester. For chromosomal anomalies such as (trisomy 21), which increases risks for heart and gastrointestinal defects, between weeks 15-20 samples for karyotyping, confirming the extra in nearly 100% of cases. This procedure, guided by , carries a low risk (0.1-0.3%) but provides definitive diagnosis, guiding parental decisions. Critical periods represent windows of heightened vulnerability to teratogens, when specific structures are forming. During the embryonic phase, particularly weeks 3-8, exposures can cause irreversible damage; for example, alcohol consumption in the first trimester disrupts migration and facial development, leading to fetal alcohol syndrome (FAS) with characteristic craniofacial dysmorphology, growth retardation, and neurobehavioral impairments. FAS affects up to 1-3 per 1,000 births in high-risk populations, underscoring the need for abstinence recommendations. These periods align with , where even brief exposures can yield lifelong consequences, emphasizing preconception and prenatal counseling.

Regenerative Medicine and Stem Cell Research

Embryonic stem cells (ESCs) are derived from the inner cell mass of the blastocyst, exhibiting pluripotency that allows them to differentiate into all three germ layers and potentially any cell type in the body. In 1998, James Thomson's team first isolated human ESCs from surplus IVF embryos, marking a pivotal advancement in regenerative potential but sparking intense ethical debates over embryo destruction and the moral status of early human life. These concerns led to federal funding restrictions in the U.S. until 2009, though research progressed internationally, highlighting the tension between therapeutic promise and bioethical principles. To circumvent ethical issues with ESCs, and colleagues developed induced pluripotent stem cells (iPSCs) in 2006 by reprogramming mouse somatic cells using four transcription factors: Oct4, , , and c-Myc. This process reactivates endogenous pluripotency networks, enabling adult cells like fibroblasts to revert to an embryonic-like state capable of self-renewal and multilineage differentiation, without requiring embryos. Human iPSCs followed in 2007, expanding accessibility for while reducing ethical barriers, as the method relies on patient-derived cells. Stem cell technologies have transformed through applications like models, which are three-dimensional, self-organizing structures grown from ESCs or iPSCs that mimic organ architecture and function for studying diseases such as and Alzheimer's. These s provide insights into developmental pathologies and drug responses in a human-relevant context, surpassing traditional 2D cultures by recapitulating tissue complexity and microenvironmental cues. In therapeutic contexts, iPSC-derived (RPE) cells have been transplanted subretinally to treat age-related ; a 2017 Japanese phase I trial demonstrated safety and partial vision restoration in a with wet AMD, with no tumor formation observed over two years. Insights from regeneration, particularly the —a mass of dedifferentiated cells formed after limb in salamanders—offer blueprints for enhancing mammalian repair by identifying key signaling pathways like Wnt and FGF that promote epimorphic regeneration. Unlike mammals, which scar rather than regenerate, amphibians rebuild complex structures through blastema-mediated proliferation, informing strategies to activate similar processes in humans for and tissue replacement. Recent 2020s clinical trials underscore progress in cardiac repair using iPSC-derived cardiomyocytes (iPSC-CMs), which integrate into host tissue to improve contractility post-myocardial . A 2023 phase I in transplanted autologous iPSC-CM sheets into patients with severe ischemic , showing improved left ventricular and no arrhythmias after one year. Ongoing international efforts, including U.S. and , focus on allogeneic iPSC-CMs with immune evasion modifications to scale therapy for , addressing scalability challenges through production. As of 2025, integrations of gene editing technologies like with iPSCs have advanced regenerative therapies, enabling precise corrections of genetic defects in stem cell-derived tissues for conditions such as and inherited cardiomyopathies. Future directions in regenerative medicine emphasize bioengineering embryonic-like environments to induce limb regrowth, combining scaffolds, growth factors, and stem cells to recreate formation in mammals. Advances in bioprinting and bioactive hydrogels aim to guide iPSC differentiation toward limb progenitors, with preclinical models in frogs demonstrating functional regrowth using wearable bioreactors that deliver timed bioactive cues, paving the way for applications by 2030.

References

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