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Human embryogenesis is the process of cell division and cellular differentiation of the embryo that occurs during the early stages of development. In biological terms, human development entails growth from a one celled zygote to an adult human being. Fertilisation occurs when the sperm cell successfully enters and fuses with an egg cell (ovum). The genetic material of the sperm and egg then combine to form a single cell called a zygote and the germinal stage of prenatal development commences.Embryogenesis covers the first eight weeks of development and at the beginning of the ninth week the embryo is termed a fetus. Human embryology is the study of this development during the first eight weeks after fertilisation. The normal period of gestation (pregnancy) is nine months or 38 weeks.
During this stage, the zygote, which is defined as an embryo because it contains a full complement of genetic material, begins to divide, in a process called cleavage. A blastocyst is then formed and implanted in the uterus. Embryogenesis continues with the next stage of gastrulation when the three germ layers of the embryo form in a process called histogenesis, and the processes of neurulation and organogenesis follow. The embryo is referred to as a fetus in the later stages of prenatal development, usually taken to be at the beginning of the ninth week. In comparison to the embryo, the fetus has more recognizable external features, and a more complete set of developing organs. The entire process of embryogenesis involves coordinated spatial and temporal changes in gene expression, cell growth and cellular differentiation. A nearly identical process occurs in other species, especially among chordates.
Fertilization takes place when the spermatozoon has successfully entered the ovum and the two sets of genetic material carried by the gametes, fuse together, resulting in the zygote, (a single diploid cell). This usually takes place in the ampulla of one of the fallopian tubes. Successful fertilisation is enabled by three processes which also act as controls to ensure species-specificity. The first is that of chemotaxis which directs the movement of the sperm towards the ovum. Secondly there is an adhesive compatibility between the sperm and the egg. With the sperm adhered to the ovum, the third process of acrosomal reaction takes place; the front part of the spermatozoon head is capped by an acrosome which contains digestive enzymes to break down the zona pellucida and allow its entry. The entry of the sperm causes calcium to be released which blocks entry to other sperm cells. A parallel reaction takes place in the ovum called the zona reaction. This sees the release of cortical granules that release enzymes which digest sperm receptor proteins, thus preventing polyspermy. The granules also fuse with the plasma membrane and modify the zona pellucida in such a way as to prevent further sperm entry.
The zygote contains the combined genetic material carried by both the male and female gametes which consists of the 23 chromosomes from the nucleus of the ovum and the 23 chromosomes from the nucleus of the sperm. The 46 chromosomes undergo changes prior to the mitotic division which leads to the formation of the embryo having two cells.
This first division marks the beginning of the cleavage process which continues with the division of the first two cells by mitosis to give four cells which then divide to give eight cells and so on. This is quite a slow process taking from 12 to 24 hours for each division. The dividing cells which are termed blastomeres (blastos Greek for sprout) are still enclosed within the strong membrane of glycoproteins (termed the zona pellucida) of the ovum, which the successful spermatozoon managed to penetrate. The zygote (which is large compared to any other cell) undergoes further cleavage, increasing the number of cells without any increase in the size of the initial zygote. This means that the proportion of nuclear genetic material is greater than that of the cytoplasm in each cell. When eight blastomeres have formed they are undifferentiated and aggregated into a sphere, and when the cells number about sixteen or thirty-two the solid sphere of cells is termed a morula. At this stage the cells start to bind firmly together in a process called compaction, and cleavage continues as cellular differentiation begins.
Cleavage itself is the first stage in blastulation, the process of forming the blastocyst. Cells differentiate into an outer layer of cells, the trophoblasts, and an inner cell mass. With further compaction the individual outer blastomeres, the trophoblasts, become indistinguishable, and are still enclosed within the zona pellucida. This compaction serves to make the structure watertight since the cells will later secrete fluid. The inner mass of cells differentiate to become embryoblasts and polarise at one end. They close together and form gap junctions in order to facilitate cellular communication. This polarisation leaves a cavity, the blastocoel in which is now termed the blastocyst. (In animals other than mammals, this is called the blastula). The trophoblasts secrete fluid into the blastocoel. By this time the size of the blastocyst has increased which makes it 'hatch' through the zona pellucida which then disintegrates.
The inner cell mass will give rise to the embryo proper, the amnion, yolk sac and allantois, while the fetal part of the placenta will form from the outer trophoblast layer. The embryo plus its membranes is called the conceptus and by this stage the conceptus is in the uterus. The zona pellucida ultimately disappears completely, and the now exposed cells of the trophoblast allow the blastocyst to attach itself to the endometrium, where it will implant.
After ovulation, the endometrial lining becomes transformed into a secretory lining in preparation of accepting the embryo. It becomes thickened with its secretory glands becoming elongated, and is increasingly vascular. This lining of the uterine cavity (or womb), is now known as the decidua and it produces a great number of large decidual cells in its increased interglandular tissue. The trophoblast then differentiates into an inner layer, the cytotrophoblast and an outer layer, the syncytiotrophoblast. The cytotrophoblast contains cuboidal epithelial cells having cell boundaries and are the source of dividing cells and the syncytiotrophoblast is a layer without cell boundaries.
The syncytiotrophoblast implants the blastocyst in the decidual epithelium, by projections of chorionic villi forming the embryonic part of the placenta. The placenta develops once the blastocyst is implanted, and forms to connect the embryo to the uterine wall. The decidua here is termed the decidua basalis and lies between the blastocyst and the myometrium and forms the maternal part of the placenta. The implantation is assisted by hydrolytic enzymes that erode the epithelium. The syncytiotrophoblast also produces human chorionic gonadotropin (hCG), a hormone that stimulates the release of progesterone from the corpus luteum. Progesterone enriches the uterus with a thick lining of blood vessels and capillaries so that it can sustain the developing embryo. The villi begin to branch and contain blood vessels of the embryo. Arteries in the decidua are remodelled to increase the maternal blood flow into the intervillous spaces of the placenta, allowing gas exchange to take place as well as the transfer of nutrients to the embryo. Waste products from the embryo will diffuse across the placenta.
As the syncytiotrophoblast starts to penetrate the uterine wall, the inner cell mass (embryoblast) also develops. The inner cell mass is the source of embryonic stem cells, which are pluripotent and can develop into any one of the three germ layer cells.
The embryoblast forms an embryonic disc which is a bilaminar disc of two layers, an upper layer the epiblast (primitive ectoderm), and a lower layer the hypoblast (primitive endoderm). The disc is stretched between what will become the amniotic cavity and the yolk sac. The epiblast is adjacent to the trophoblast and made of columnar cells; the hypoblast is closest to the blastocyst cavity, and made of cuboidal cells. The epiblast migrates away from the trophoblast downwards, forming the amniotic cavity, the lining of which is formed from amnioblasts developed from the epiblast. The hypoblast is pushed down and forms the yolk sac (exocoelomic cavity) lining. Some hypoblast cells migrate along the inner cytotrophoblast lining of the blastocoel, secreting an extracellular matrix along the way. These hypoblast cells and extracellular matrix are called Heuser's membrane (or exocoelomic membrane), and they cover the blastocoel to form the yolk sac (or exocoelomic cavity). Cells of the epiblast migrate along the outer edges of this reticulum and form the extraembryonic mesoderm, which makes it difficult to maintain the extraembryonic reticulum. Soon pockets form in the reticulum, which ultimately coalesce to form the chorionic cavity or extraembryonic coelom.
The primitive streak, a linear band of cells formed by the migrating epiblast, appears, and this marks the beginning of gastrulation, which takes place around the sixteenth day (week 3) after fertilisation. The process of gastrulation reorganises the two-layer embryo into a three-layer embryo, and also gives the embryo its specific dorsal-ventral and anterior-posterior orientation, by way of the primitive streak which establishes bilateral symmetry. A primitive node (or primitive knot) forms in front of the primitive streak which is the organiser of neurulation. A primitive pit forms as a depression in the centre of the primitive node which connects to the notochord which lies directly underneath. The node has arisen from epiblasts of the amniotic cavity floor, and it is this node that induces the formation of the neural plate which serves as the basis for the nervous system. The neural plate will form opposite the primitive streak from ectodermal tissue which thickens and flattens into the neural plate. The epiblast in that region moves down into the streak at the location of the primitive pit where the process called ingression, which leads to the formation of the mesoderm takes place. This ingression sees the cells from the epiblast move into the primitive streak in an epithelial-mesenchymal transition; epithelial cells become mesenchymal stem cells, multipotent stromal cells that can differentiate into various cell types. The hypoblast is pushed out of the way and goes on to form the amnion.The epiblast keeps moving and forms a second layer, the mesoderm. The epiblast has now differentiated into the three germ layers of the embryo, so that the bilaminar disc is now a trilaminar disc, the gastrula.
The three germ layers are the ectoderm, mesoderm and endoderm, and are formed as three overlapping flat discs. It is from these three layers that all the structures and organs of the body will be derived through the processes of histogenesis and organogenesis. The upper layer of ectoderm will give rise to the outermost layer of skin, central and peripheral nervous systems, eyes, inner ear, and many connective tissues. The middle layer of mesoderm will give rise to the heart and the beginning of the circulatory system as well as the bones, muscles and kidneys. The inner layer of endoderm will serve as the starting point for the development of the lungs, intestine and bladder.
Following ingression, a blastopore develops where the cells have ingressed, in one side of the embryo and it deepens to become the archenteron, the first formative stage of the gut. The blastopore becomes the anus whist the gut tunnels through the embryo to the other side where the opening becomes the mouth. With a functioning digestive tube, gastrulation is now completed and the next stage of neurulation can begin.
Following gastrulation, the ectoderm gives rise to epithelial and neural tissue, and the gastrula is now referred to as the neurula. The neural plate that has formed as a thickened plate from the ectoderm, continues to broaden and its ends start to fold upwards as neural folds. Neurulation refers to this folding process whereby the neural plate is transformed into the neural tube.They fold, along a shallow neural groove which has formed as a dividing median line in the neural plate. This deepens as the folds continue to gain height when they will meet and close together. The cranial and caudal neuropores become progressively smaller until they close completely (by day 26) forming the neural tube.
Toxic exposures during the germinal stage may cause prenatal death resulting in a miscarriage, but do not cause developmental defects. However, toxic exposures in the embryonic period can be the cause of major congenital malformations, since the precursors of the major organ systems are now developing.
Each cell of the preimplantation embryo is pluripotent. That is, each cell has the potential to form all of the different cell types in the developing embryo. This cell potency means that some cells can be removed from the preimplantation embryo and the remaining cells will compensate for their absence. This has allowed the development of a technique known as preimplantation genetic diagnosis (PGD), whereby a small number of cells from the preimplantation embryo created by IVF, can be removed by biopsy and subjected to genetic diagnosis. This allows embryos that are not affected by defined genetic diseases to be selected and then transferred to the mother's uterus.
- Developmental biology
- Mammalian embryogenesis
- Potential person
- Recapitulation theory
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|Wikimedia Commons has media related to Human embryos.|
- Photo of blastocyst in utero
- Slideshow: In the Womb
- Online course in embryology for medicine students developed by the universities of Fribourg, Lausanne and Bern