{"id":1111,"date":"2021-01-27T23:24:38","date_gmt":"2021-01-27T23:24:38","guid":{"rendered":"https:\/\/pressbooks.publishdot.com\/anatomyphysiology\/chapter\/16-2-embryonic-development\/"},"modified":"2021-12-07T10:35:14","modified_gmt":"2021-12-07T10:35:14","slug":"16-2-embryonic-development","status":"publish","type":"chapter","link":"https:\/\/pressbooks.publishdot.com\/anatomyphysiology\/chapter\/16-2-embryonic-development\/","title":{"raw":"16.2 Embryonic Development","rendered":"16.2 Embryonic Development"},"content":{"raw":"
\n

Learning Objectives<\/strong><\/p>\n\n<\/header>\n

\n\nBy the end of this section, you will be able to:\n
    \n \t
  • Distinguish the stages of embryonic development that occur before implantation<\/li>\n \t
  • Describe the process of implantation<\/li>\n \t
  • List and describe four embryonic membranes<\/li>\n \t
  • Explain gastrulation<\/li>\n \t
  • Describe how the placenta is formed and identify its functions<\/li>\n \t
  • Explain how an embryo transforms from a flat disc of cells into a three-dimensional shape resembling a human<\/li>\n \t
  • Summarise the process of organogenesis<\/li>\n<\/ul>\n<\/div>\n<\/div>\nThroughout this chapter, we will express embryonic and foetal ages in terms of weeks from fertilisation, commonly called conception. The period of time required for full development of a foetus<\/strong> in utero<\/em> is referred to as gestation<\/strong> (gestare = \u201cto carry\u201d or \u201cto bear\u201d). It can be subdivided into distinct gestational periods. The first 2 weeks of prenatal development are referred to as the pre-embryonic stage. A developing human is referred to as an embryo<\/strong> during weeks 3\u20138 and a foetus from the ninth week of gestation until birth. In this section, we\u2019ll cover the pre-embryonic and embryonic stages of development, which are characterised by cell division, migration, and differentiation. By the end of the embryonic period, all the organ systems are structured in rudimentary form, although the organs themselves are either non-functional or only semi-functional.\n

    Pre-Implantation Embryonic Development<\/h2>\nFollowing fertilisation, the zygote and its associated membranes, together referred to as the conceptus<\/strong>, continue to be projected toward the uterus by peristalsis and beating cilia. During its journey to the uterus, the zygote undergoes five or six rapid mitotic cell divisions. Although each cleavage<\/strong> results in more cells, it does not increase the total volume of the conceptus (Figure 16.2.1). Each daughter cell produced by cleavage is called a blastomere<\/strong> (blastos = \u201cgerm,\u201d in the sense of a seed or sprout).\n\nApproximately three days after fertilisation, a 16-cell conceptus reaches the uterus. The cells that had been loosely grouped are now compacted and look more like a solid mass. The name given to this structure is the morula<\/strong> (morula = \u201clittle mulberry\u201d). Once inside the uterus, the conceptus floats freely for several more days. It continues to divide, creating a ball of approximately 100 cells, and consuming nutritive endometrial secretions called uterine milk while the uterine lining thickens. The ball of now tightly bound cells starts to secrete fluid and organise themselves around a fluid-filled cavity, the blastocoel<\/strong>. At this developmental stage, the conceptus is referred to as a blastocyst<\/strong>. Within this structure, a group of cells forms into an inner cell mass<\/strong>, which is fated to become the embryo. The cells that form the outer shell are called trophoblasts (trophe = \u201cto feed\u201d or \u201cto nourish\u201d). These cells will develop into the chorionic sac and the foetal portion of the placenta<\/strong> (the organ of nutrient, waste and gas exchange between mother and the developing offspring).\n\nThe inner mass of embryonic cells is totipotent during this stage, meaning that each cell has the potential to differentiate into any cell type in the human body. Totipotency lasts for only a few days before the cells\u2019 fates are set as being the precursors to a specific lineage of cells.\n\n[caption id=\"attachment_1110\" align=\"aligncenter\" width=\"1024\"]\"Pre-embryonic Figure 16.2.1. Pre-embryonic cleavages.<\/strong> Pre-embryonic cleavages make use of the abundant cytoplasm of the conceptus as the cells rapidly divide without changing the total volume.[\/caption]\n\nAs the blastocyst forms, the trophoblast excretes enzymes that begin to degrade the zona pellucida. In a process called \u201chatching,\u201d the conceptus breaks free of the zona pellucida in preparation for implantation<\/strong>.\n

    Implantation<\/h2>\nAt the end of the first week, the blastocyst comes in contact with the uterine wall and adheres to it, embedding itself in the uterine lining via the trophoblast cells. Thus, begins the process of implantation, which signals the end of the pre-embryonic stage of development (Figure 16.2.2). Implantation can be accompanied by minor bleeding. The blastocyst typically implants in the fundus of the uterus or on the posterior wall. However, if the endometrium is not fully developed and ready to receive the blastocyst, the blastocyst will detach and find a better spot. A significant percentage (50\u201375 percent) of blastocysts fail to implant; when this occurs, the blastocyst is shed with the endometrium during menses. The high rate of implantation failure is one reason why pregnancy typically requires several ovulation cycles to achieve.\n\n[caption id=\"attachment_1110\" align=\"aligncenter\" width=\"1024\"]\"Diagram Figure 16.2.2. Pre-embryonic development.<\/strong> Ovulation, fertilisation, pre-embryonic development, and implantation occur at specific locations within the female reproductive system in a time span of approximately one week.[\/caption]\n\nWhen implantation succeeds and the blastocyst adheres to the endometrium, the superficial cells of the trophoblast<\/strong> fuse with each other, forming the syncytiotrophoblast<\/strong>, a multinucleated body that digests endometrial cells to firmly secure the blastocyst to the uterine wall. In response, the uterine mucosa rebuilds itself and envelops the blastocyst (Figure 16.2.3). The trophoblast secretes human chorionic gonadotropin (hCG)<\/strong>, a hormone that directs the corpus luteum to survive, enlarge, and continue producing progesterone and oestrogen to suppress menses. These functions of hCG are necessary for creating an environment suitable for the developing embryo. As a result of this increased production, hCG accumulates in the maternal bloodstream and is excreted in the urine. Implantation is complete by the middle of the second week. Just a few days after implantation, the trophoblast has secreted enough hCG for an at-home urine pregnancy test to give a positive result.\n\n[caption id=\"attachment_1110\" align=\"aligncenter\" width=\"818\"]\"Diagram Figure 16.2.3. Implantation.<\/strong> During implantation, the trophoblast cells of the blastocyst adhere to the endometrium and digest endometrial cells until it is attached securely.[\/caption]\n\nMost of the time an embryo implants within the body of the uterus in a location that can support growth and development. However, in one to two percent of cases, the embryo implants either outside the uterus (an ectopic pregnancy<\/strong>) or in a region of uterus that can create complications for the pregnancy. If the embryo implants in the inferior portion of the uterus, the placenta can potentially grow over the opening of the cervix, a condition call placenta previa<\/strong>.\n

    Disorders of the Development of the Embryo<\/h2>\nIn the vast majority of ectopic pregnancies, the embryo does not complete its journey to the uterus and implants in the uterine tube, referred to as a tubal pregnancy. However, there are also ovarian ectopic pregnancies (in which the egg never left the ovary) and abdominal ectopic pregnancies (in which an egg was \u201clost\u201d to the abdominal cavity during the transfer from ovary to uterine tube, or in which an embryo from a tubal pregnancy re-implanted in the abdomen). Once in the abdominal cavity, an embryo can implant into any well-vascularised structure\u2014the rectouterine cavity (Douglas\u2019 pouch), the mesentery of the intestines, and the greater omentum are some common sites.\n\nTubal pregnancies can be caused by scar tissue within the tube following a sexually transmitted bacterial infection. The scar tissue impedes the progress of the embryo into the uterus\u2014in some cases \u201csnagging\u201d the embryo and, in other cases, blocking the tube completely. Approximately one half of tubal pregnancies resolve spontaneously. Implantation in a uterine tube causes bleeding, which appears to stimulate smooth muscle contractions and expulsion of the embryo. In the remaining cases, medical or surgical intervention is necessary. If an ectopic pregnancy is detected early, the embryo\u2019s development can be arrested by the administration of the cytotoxic drug methotrexate, which inhibits the metabolism of folic acid. If diagnosis is late and the uterine tube is already ruptured, surgical repair is essential.\n\nEven if the embryo has successfully found its way to the uterus, it does not always implant in an optimal location (the fundus or the posterior wall of the uterus). Placenta previa can result if an embryo implants close to the internal os of the uterus (the internal opening of the cervix). As the foetus grows, the placenta can partially or completely cover the opening of the cervix (Figure 16.2.4). Although it occurs in only 0.5 percent of pregnancies, placenta previa is the leading cause of antepartum haemorrhage (profuse vaginal bleeding after week 24 of pregnancy but prior to childbirth).\n\n[caption id=\"attachment_1110\" align=\"aligncenter\" width=\"1024\"]\"Placenta Figure 16.2.4. Placenta previa.<\/strong> An embryo that implants too close to the opening of the cervix can lead to placenta previa, a condition in which the placenta partially or completely covers the cervix.[\/caption]\n

    Embryonic Membranes<\/h2>\nDuring the second week of development, with the embryo implanted in the uterus, cells within the blastocyst start to organise into layers. Some grow to form the extra-embryonic membranes needed to support and protect the growing embryo: the amnion<\/strong>, the yolk sac<\/strong>, the allantois<\/strong>, and the chorion.<\/strong>\n\nAt the beginning of the second week, the cells of the inner cell mass form into a two-layered disc of embryonic cells, and a space\u2014the amniotic cavity<\/strong>\u2014opens between it and the trophoblast (Figure 16.2.5). Cells from the upper layer of the disc (the epiblast<\/strong>) extend around the amniotic cavity, creating a membranous sac that forms into the amnion by the end of the second week. The amnion fills with amniotic fluid and eventually grows to surround the embryo. Early in development, amniotic fluid consists almost entirely of a filtrate of maternal plasma, but as the kidneys of the foetus begin to function at approximately the eighth week, they add urine to the volume of amniotic fluid. Floating within the amniotic fluid, the embryo\u2014and later, the foetus\u2014is protected from trauma and rapid temperature changes. It can move freely within the fluid and can prepare for swallowing and breathing out of the uterus.\n\n[caption id=\"attachment_1110\" align=\"aligncenter\" width=\"1024\"]\"Development Figure 16.2.5. Development of the embryonic disc<\/strong>. Formation of the embryonic disc leaves spaces on either side that develop into the amniotic cavity and the yolk sac.[\/caption]\n\nOn the ventral side of the embryonic disc, opposite the amnion, cells in the lower layer of the embryonic disk (the hypoblast<\/strong>) extend into the blastocyst cavity and form a yolk sac. The yolk sac supplies some nutrients absorbed from the trophoblast and provides primitive blood circulation to the developing embryo for the second and third week of development. When the placenta takes over nourishing the embryo at approximately week 4, the yolk sac has been greatly reduced in size and its main function is to serve as the source of blood cells and germ cells (cells that will give rise to gametes). During week 3, a finger-like out-pocketing of the yolk sac develops into the allantois, a primitive excretory duct of the embryo that will become part of the urinary bladder. Together, the stalks of the yolk sac and allantois establish the outer structure of the umbilical cord.<\/strong>\n\nThe last of the extra-embryonic membranes is the chorion, which is the one membrane that surrounds all others. The development of the chorion will be discussed in more detail shortly, as it relates to the growth and development of the placenta.\n

    Embryogenesis<\/h2>\nAs the third week of development begins, the two-layered disc of cells becomes a three-layered disc through the process of gastrulation<\/strong>, during which the cells transition from totipotency to multipotency. The embryo, which takes the shape of an oval-shaped disc, forms an indentation called the primitive streak<\/strong> along the dorsal surface of the epiblast. A node at the caudal or \u201ctail\u201d end of the primitive streak emits growth factors that direct cells to multiply and migrate. Cells migrate toward and through the primitive streak and then move laterally to create two new layers of cells. The first layer is the endoderm<\/strong>, a sheet of cells that displaces the hypoblast and lies adjacent to the yolk sac. The second layer of cells fills in as the middle layer, or mesoderm<\/strong>. The cells of the epiblast that remain (not having migrated through the primitive streak) become the ectoderm<\/strong> (Figure 16.2.6).\n\n[caption id=\"attachment_1110\" align=\"aligncenter\" width=\"1024\"]\"Diagram Figure 16.2.6. Germ layers.<\/strong> Formation of the three primary germ layers occurs during the first 2 weeks of development. The embryo at this stage is only a few millimetres in length.[\/caption]\n\nEach of these germ layers will develop into specific structures in the embryo. Whereas the ectoderm and endoderm form tightly connected epithelial sheets, the mesodermal cells are less organised and exist as a loosely connected cell community. The ectoderm gives rise to cell lineages that differentiate to become the central and peripheral nervous systems, sensory organs, epidermis, hair and nails. Mesodermal cells ultimately become the skeleton, muscles, connective tissue, heart, blood vessels and kidneys. The endoderm goes on to form the epithelial lining of the gastrointestinal tract, liver and pancreas, as well as the lungs (Figure 16.2.7).\n\n[caption id=\"attachment_1110\" align=\"aligncenter\" width=\"1024\"]\"Fates Figure 16.2.7. Fates of germ layers in embryo.<\/strong> Following gastrulation of the embryo in the third week, embryonic cells of the ectoderm, mesoderm, and endoderm begin to migrate and differentiate into the cell lineages that will give rise to mature organs and organ systems in the infant.[\/caption]\n

    Development of the Placenta<\/h2>\nDuring the first several weeks of development, the cells of the endometrium\u2014referred to as decidual cells\u2014nourish the nascent embryo. During prenatal weeks 4\u201312, the developing placenta gradually takes over the role of feeding the embryo and the decidual cells are no longer needed. The mature placenta is composed of tissues derived from the embryo, as well as maternal tissues of the endometrium. The placenta connects to the conceptus via the umbilical cord, which carries deoxygenated blood and wastes from the foetus through two umbilical arteries; nutrients and oxygen are carried from the mother to the foetus through the single umbilical vein. The umbilical cord is surrounded by the amnion and the spaces within the cord around the blood vessels are filled with Wharton\u2019s jelly, a mucous connective tissue.\n\nThe maternal portion of the placenta develops from the deepest layer of the endometrium, the decidua basalis. To form the embryonic portion of the placenta, the syncytiotrophoblast and the underlying cells of the trophoblast (cytotrophoblast cells) begin to proliferate along with a layer of extraembryonic mesoderm cells. These form the chorionic membrane<\/strong>, which envelops the entire conceptus as the chorion. The chorionic membrane forms finger-like structures called chorionic villi<\/strong> that burrow into the endometrium like tree roots, making up the foetal portion of the placenta. The cytotrophoblast cells perforate the chorionic villi, burrow farther into the endometrium, and remodel maternal blood vessels to augment maternal blood flow surrounding the villi. Meanwhile, foetal mesenchymal cells derived from the mesoderm fill the villi and differentiate into blood vessels, including the three umbilical blood vessels that connect the embryo to the developing placenta (Figure 16.2.8).\n\n \n\n[caption id=\"attachment_1110\" align=\"aligncenter\" width=\"1024\"]\"Cross-section Figure 16.2.8. Cross-section of the placenta.<\/strong> In the placenta, maternal and foetal blood components are conducted through the surface of the chorionic villi, but maternal and foetal bloodstreams never mix directly.[\/caption]\n\nThe placenta develops throughout the embryonic period and during the first several weeks of the foetal period; placentation<\/strong> is complete by weeks 14\u201316. As a fully developed organ, the placenta provides nutrition and excretion, respiration and endocrine function (Table 16.2.1 and Figure 16.2.9). It receives blood from the foetus through the umbilical arteries. Capillaries in the chorionic villi filter foetal wastes out of the blood and return clean, oxygenated blood to the foetus through the umbilical vein. Nutrients and oxygen are transferred from maternal blood surrounding the villi through the capillaries and into the foetal bloodstream. Some substances move across the placenta by simple diffusion. Oxygen, carbon dioxide, and any other lipid-soluble substances take this route. Other substances move across by facilitated diffusion. This includes water-soluble glucose. The foetus has a high demand for amino acids and iron, and those substances are moved across the placenta by active transport.\n\n[caption id=\"attachment_1110\" align=\"alignright\" width=\"300\"]\"Photo Figure 16.2.9. Placenta.<\/strong> This post-expulsion placenta and umbilical cord (white) are viewed from the foetal side.[\/caption]\n\nMaternal and foetal blood does not commingle because blood cells cannot move across the placenta. This separation prevents the mother\u2019s cytotoxic T cells from reaching and subsequently destroying the foetus, which bears \u201cnon-self\u201d antigens. Further, it ensures the foetal red blood cells do not enter the mother\u2019s circulation and trigger antibody development (if they carry \u201cnon-self\u201d antigens)\u2014at least until the final stages of pregnancy or birth. This is the reason that, even in the absence of preventive treatment, an Rh\u2212 mother doesn\u2019t develop antibodies that could cause haemolytic disease in her first Rh+ foetus.\n\nAlthough blood cells are not exchanged, the chorionic villi provide ample surface area for the two-way exchange of substances between maternal and foetal blood. The rate of exchange increases throughout gestation as the villi become thinner and increasingly branched. The placenta is permeable to lipid-soluble fetotoxic substances: alcohol, nicotine, barbiturates, antibiotics, certain pathogens, and many other substances that can be dangerous or fatal to the developing embryo or foetus. For these reasons, pregnant women should avoid foetotoxic substances. Alcohol consumption by pregnant women, for example, can result in a range of abnormalities referred to as foetal alcohol spectrum disorders (FASD). These include organ and facial malformations, as well as cognitive and behavioural disorders.\n\nTable 16.2.1<\/strong>. Functions of the placenta\n\n\n\n\n\n\n
    Nutrition and digestion<\/strong><\/td>\nRespiration<\/strong><\/td>\nEndocrine function<\/strong><\/td>\n<\/tr>\n
    Mediates diffusion of maternal glucose, amino acids, fatty acids, vitamins and minerals<\/td>\nMediates maternal-to-foetal oxygen transport and foetal-to-maternal carbon dioxide transport<\/td>\nSecretes several hormones, including hCG, oestrogens and progesterone to maintain the pregnancy and stimulate maternal and foetal development<\/td>\n<\/tr>\n
    Stores nutrients during early to accommodate increased foetal demand later in pregnancy<\/td>\n<\/td>\nMediates the transmission of maternal hormones into foetal blood and vice versa<\/td>\n<\/tr>\n
    Excretes and filters foetal nitrogenous wastes into maternal blood<\/td>\n<\/td>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

    Organogenesis<\/h2>\nFollowing gastrulation, rudiments of the central nervous system develop from the ectoderm in the process of neurulation<\/strong> (Figure 16.2.10). Specialised neuroectodermal tissues along the length of the embryo thicken into the neural plate<\/strong>. During the fourth week, tissues on either side of the plate fold upward into a neural fold<\/strong>. The two folds converge to form the neural tube<\/strong>. The tube lies atop a rod-shaped, mesoderm-derived notochord<\/strong>, which eventually becomes the nucleus pulposus of intervertebral discs. Block-like structures called somites<\/strong> form on either side of the tube, eventually differentiating into the axial skeleton, skeletal muscle and dermis. During the fourth and fifth weeks, the anterior neural tube dilates and subdivides to form vesicles that will become the brain structures.\n\nFolate, one of the B vitamins, is important to the healthy development of the neural tube. A deficiency of maternal folate in the first weeks of pregnancy can result in neural tube defects, including spina bifida\u2014a birth defect in which spinal tissue protrudes through the newborn\u2019s vertebral column which has failed to completely close. A more severe neural tube defect is anencephaly, a partial or complete absence of brain tissue.\n\n \n\n[caption id=\"attachment_1110\" align=\"aligncenter\" width=\"886\"]\"Diagram Figure 16.2.10. Neurulation.<\/strong> The embryonic process of neurulation establishes the rudiments of the future central nervous system and skeleton.[\/caption]\n\nThe embryo, which begins as a flat sheet of cells, begins to acquire a cylindrical shape through the process of embryonic folding<\/strong> (Figure 16.2.11). The embryo folds laterally and again at either end, forming a C-shape with distinct head and tail ends. The embryo envelops a portion of the yolk sac, which protrudes with the umbilical cord from what will become the abdomen. The folding essentially creates a tube, called the primitive gut, that is lined by the endoderm. The amniotic sac, which was sitting on top of the flat embryo, envelops the embryo as it folds.\n\n[caption id=\"attachment_1110\" align=\"aligncenter\" width=\"1024\"]\"Diagram Figure 16.2.11. Embryonic folding.<\/strong> Embryonic folding converts a flat sheet of cells into a hollow, tube-like structure.[\/caption]\n\nWithin the first eight weeks of gestation, a developing embryo establishes the rudimentary structures of all its organs and tissues from the ectoderm, mesoderm and endoderm. This process is called organogenesis.<\/strong>\n\n[caption id=\"attachment_1110\" align=\"alignright\" width=\"281\"]\"Embryo Figure 16.2.12. Embryo at seven weeks.<\/strong> An embryo at the end of seven weeks of development is only 10 mm in length, but its developing eyes, limb buds, and tail are already visible. (This embryo was derived from an ectopic pregnancy.) (credit: Ed Uthman).[\/caption]\n\nLike the central nervous system, the heart also begins its development in the embryo as a tube-like structure, connected via capillaries to the chorionic villi. Cells of the primitive tube-shaped heart are capable of electrical conduction and contraction. The heart begins beating in the beginning of the fourth week, although it does not actually pump embryonic blood until a week later, when the oversized liver has begun producing red blood cells. (This is a temporary responsibility of the embryonic liver that the bone marrow will assume during foetal development.) During weeks four\u2013five, the eye pits form, limb buds become apparent and the rudiments of the pulmonary system are formed.\n\nDuring the sixth week, uncontrolled foetal limb movements begin to occur. The gastrointestinal system develops too rapidly for the embryonic abdomen to accommodate it and the intestines temporarily loop into the umbilical cord. Paddle-shaped hands and feet develop fingers and toes by the process of apoptosis (programmed cell death), which causes the tissues between the fingers to disintegrate. By week seven, the facial structure is more complex and includes nostrils, outer ears and lenses (Figure 16.2.12). By the eighth week, the head is nearly as large as the rest of the embryo\u2019s body and all major brain structures are in place. The external genitalia are apparent, but at this point, male and female embryos are indistinguishable. Bone begins to replace cartilage in the embryonic skeleton through the process of ossification. By the end of the embryonic period, the embryo is approximately three cm from crown to rump and weighs approximately eight grams.\n
    \n

    Section Review<\/strong><\/p>\n\n<\/header>\n

    \n\nAs the zygote travels toward the uterus, it undergoes numerous cleavages in which the number of cells doubles (blastomeres). Upon reaching the uterus, the conceptus has become a tightly packed sphere of cells called the morula, which then forms into a blastocyst consisting of an inner cell mass within a fluid-filled cavity surrounded by trophoblasts. The blastocyst implants in the uterine wall, the trophoblasts fuse to form a syncytiotrophoblast, and the conceptus is enveloped by the endometrium. Four embryonic membranes form to support the growing embryo: the amnion, the yolk sac, the allantois and the chorion. The chorionic villi of the chorion extend into the endometrium to form the foetal portion of the placenta. The placenta supplies the growing embryo with oxygen and nutrients; it also removes carbon dioxide and other metabolic wastes.\n\nFollowing implantation, embryonic cells undergo gastrulation, in which they differentiate and separate into an embryonic disc and establish three primary germ layers (the endoderm, mesoderm and ectoderm). Through the process of embryonic folding, the foetus begins to take shape. Neurulation starts the process of the development of structures of the central nervous system and organogenesis establishes the basic plan for all organ systems.\n\n<\/div>\n<\/div>\n
    \n

    Review Questions<\/strong><\/p>\n\n<\/header>\n

    \n\n[h5p id=\"606\"]\n\n<\/div>\n<\/div>\n
    \n

    Critical Thinking Questions<\/strong><\/p>\n\n<\/header>\n

    \n\n[h5p id=\"607\"]\n\n[h5p id=\"608\"]\n\n<\/div>\n<\/div>\nClick the drop down below to review the terms learned from this chapter.\n\n[h5p id=\"609\"]","rendered":"
    \n
    \n

    Learning Objectives<\/strong><\/p>\n<\/header>\n

    \n

    By the end of this section, you will be able to:<\/p>\n

      \n
    • Distinguish the stages of embryonic development that occur before implantation<\/li>\n
    • Describe the process of implantation<\/li>\n
    • List and describe four embryonic membranes<\/li>\n
    • Explain gastrulation<\/li>\n
    • Describe how the placenta is formed and identify its functions<\/li>\n
    • Explain how an embryo transforms from a flat disc of cells into a three-dimensional shape resembling a human<\/li>\n
    • Summarise the process of organogenesis<\/li>\n<\/ul>\n<\/div>\n<\/div>\n

      Throughout this chapter, we will express embryonic and foetal ages in terms of weeks from fertilisation, commonly called conception. The period of time required for full development of a foetus<\/strong> in utero<\/em> is referred to as gestation<\/strong> (gestare = \u201cto carry\u201d or \u201cto bear\u201d). It can be subdivided into distinct gestational periods. The first 2 weeks of prenatal development are referred to as the pre-embryonic stage. A developing human is referred to as an embryo<\/strong> during weeks 3\u20138 and a foetus from the ninth week of gestation until birth. In this section, we\u2019ll cover the pre-embryonic and embryonic stages of development, which are characterised by cell division, migration, and differentiation. By the end of the embryonic period, all the organ systems are structured in rudimentary form, although the organs themselves are either non-functional or only semi-functional.<\/p>\n

      Pre-Implantation Embryonic Development<\/h2>\n

      Following fertilisation, the zygote and its associated membranes, together referred to as the conceptus<\/strong>, continue to be projected toward the uterus by peristalsis and beating cilia. During its journey to the uterus, the zygote undergoes five or six rapid mitotic cell divisions. Although each cleavage<\/strong> results in more cells, it does not increase the total volume of the conceptus (Figure 16.2.1). Each daughter cell produced by cleavage is called a blastomere<\/strong> (blastos = \u201cgerm,\u201d in the sense of a seed or sprout).<\/p>\n

      Approximately three days after fertilisation, a 16-cell conceptus reaches the uterus. The cells that had been loosely grouped are now compacted and look more like a solid mass. The name given to this structure is the morula<\/strong> (morula = \u201clittle mulberry\u201d). Once inside the uterus, the conceptus floats freely for several more days. It continues to divide, creating a ball of approximately 100 cells, and consuming nutritive endometrial secretions called uterine milk while the uterine lining thickens. The ball of now tightly bound cells starts to secrete fluid and organise themselves around a fluid-filled cavity, the blastocoel<\/strong>. At this developmental stage, the conceptus is referred to as a blastocyst<\/strong>. Within this structure, a group of cells forms into an inner cell mass<\/strong>, which is fated to become the embryo. The cells that form the outer shell are called trophoblasts (trophe = \u201cto feed\u201d or \u201cto nourish\u201d). These cells will develop into the chorionic sac and the foetal portion of the placenta<\/strong> (the organ of nutrient, waste and gas exchange between mother and the developing offspring).<\/p>\n

      The inner mass of embryonic cells is totipotent during this stage, meaning that each cell has the potential to differentiate into any cell type in the human body. Totipotency lasts for only a few days before the cells\u2019 fates are set as being the precursors to a specific lineage of cells.<\/p>\n

      \"Pre-embryonic
      Figure 16.2.1. Pre-embryonic cleavages.<\/strong> Pre-embryonic cleavages make use of the abundant cytoplasm of the conceptus as the cells rapidly divide without changing the total volume.<\/figcaption><\/figure>\n

      As the blastocyst forms, the trophoblast excretes enzymes that begin to degrade the zona pellucida. In a process called \u201chatching,\u201d the conceptus breaks free of the zona pellucida in preparation for implantation<\/strong>.<\/p>\n

      Implantation<\/h2>\n

      At the end of the first week, the blastocyst comes in contact with the uterine wall and adheres to it, embedding itself in the uterine lining via the trophoblast cells. Thus, begins the process of implantation, which signals the end of the pre-embryonic stage of development (Figure 16.2.2). Implantation can be accompanied by minor bleeding. The blastocyst typically implants in the fundus of the uterus or on the posterior wall. However, if the endometrium is not fully developed and ready to receive the blastocyst, the blastocyst will detach and find a better spot. A significant percentage (50\u201375 percent) of blastocysts fail to implant; when this occurs, the blastocyst is shed with the endometrium during menses. The high rate of implantation failure is one reason why pregnancy typically requires several ovulation cycles to achieve.<\/p>\n

      \"Diagram
      Figure 16.2.2. Pre-embryonic development.<\/strong> Ovulation, fertilisation, pre-embryonic development, and implantation occur at specific locations within the female reproductive system in a time span of approximately one week.<\/figcaption><\/figure>\n

      When implantation succeeds and the blastocyst adheres to the endometrium, the superficial cells of the trophoblast<\/strong> fuse with each other, forming the syncytiotrophoblast<\/strong>, a multinucleated body that digests endometrial cells to firmly secure the blastocyst to the uterine wall. In response, the uterine mucosa rebuilds itself and envelops the blastocyst (Figure 16.2.3). The trophoblast secretes human chorionic gonadotropin (hCG)<\/strong>, a hormone that directs the corpus luteum to survive, enlarge, and continue producing progesterone and oestrogen to suppress menses. These functions of hCG are necessary for creating an environment suitable for the developing embryo. As a result of this increased production, hCG accumulates in the maternal bloodstream and is excreted in the urine. Implantation is complete by the middle of the second week. Just a few days after implantation, the trophoblast has secreted enough hCG for an at-home urine pregnancy test to give a positive result.<\/p>\n

      \"Diagram
      Figure 16.2.3. Implantation.<\/strong> During implantation, the trophoblast cells of the blastocyst adhere to the endometrium and digest endometrial cells until it is attached securely.<\/figcaption><\/figure>\n

      Most of the time an embryo implants within the body of the uterus in a location that can support growth and development. However, in one to two percent of cases, the embryo implants either outside the uterus (an ectopic pregnancy<\/strong>) or in a region of uterus that can create complications for the pregnancy. If the embryo implants in the inferior portion of the uterus, the placenta can potentially grow over the opening of the cervix, a condition call placenta previa<\/strong>.<\/p>\n

      Disorders of the Development of the Embryo<\/h2>\n

      In the vast majority of ectopic pregnancies, the embryo does not complete its journey to the uterus and implants in the uterine tube, referred to as a tubal pregnancy. However, there are also ovarian ectopic pregnancies (in which the egg never left the ovary) and abdominal ectopic pregnancies (in which an egg was \u201clost\u201d to the abdominal cavity during the transfer from ovary to uterine tube, or in which an embryo from a tubal pregnancy re-implanted in the abdomen). Once in the abdominal cavity, an embryo can implant into any well-vascularised structure\u2014the rectouterine cavity (Douglas\u2019 pouch), the mesentery of the intestines, and the greater omentum are some common sites.<\/p>\n

      Tubal pregnancies can be caused by scar tissue within the tube following a sexually transmitted bacterial infection. The scar tissue impedes the progress of the embryo into the uterus\u2014in some cases \u201csnagging\u201d the embryo and, in other cases, blocking the tube completely. Approximately one half of tubal pregnancies resolve spontaneously. Implantation in a uterine tube causes bleeding, which appears to stimulate smooth muscle contractions and expulsion of the embryo. In the remaining cases, medical or surgical intervention is necessary. If an ectopic pregnancy is detected early, the embryo\u2019s development can be arrested by the administration of the cytotoxic drug methotrexate, which inhibits the metabolism of folic acid. If diagnosis is late and the uterine tube is already ruptured, surgical repair is essential.<\/p>\n

      Even if the embryo has successfully found its way to the uterus, it does not always implant in an optimal location (the fundus or the posterior wall of the uterus). Placenta previa can result if an embryo implants close to the internal os of the uterus (the internal opening of the cervix). As the foetus grows, the placenta can partially or completely cover the opening of the cervix (Figure 16.2.4). Although it occurs in only 0.5 percent of pregnancies, placenta previa is the leading cause of antepartum haemorrhage (profuse vaginal bleeding after week 24 of pregnancy but prior to childbirth).<\/p>\n

      \"Placenta
      Figure 16.2.4. Placenta previa.<\/strong> An embryo that implants too close to the opening of the cervix can lead to placenta previa, a condition in which the placenta partially or completely covers the cervix.<\/figcaption><\/figure>\n

      Embryonic Membranes<\/h2>\n

      During the second week of development, with the embryo implanted in the uterus, cells within the blastocyst start to organise into layers. Some grow to form the extra-embryonic membranes needed to support and protect the growing embryo: the amnion<\/strong>, the yolk sac<\/strong>, the allantois<\/strong>, and the chorion.<\/strong><\/p>\n

      At the beginning of the second week, the cells of the inner cell mass form into a two-layered disc of embryonic cells, and a space\u2014the amniotic cavity<\/strong>\u2014opens between it and the trophoblast (Figure 16.2.5). Cells from the upper layer of the disc (the epiblast<\/strong>) extend around the amniotic cavity, creating a membranous sac that forms into the amnion by the end of the second week. The amnion fills with amniotic fluid and eventually grows to surround the embryo. Early in development, amniotic fluid consists almost entirely of a filtrate of maternal plasma, but as the kidneys of the foetus begin to function at approximately the eighth week, they add urine to the volume of amniotic fluid. Floating within the amniotic fluid, the embryo\u2014and later, the foetus\u2014is protected from trauma and rapid temperature changes. It can move freely within the fluid and can prepare for swallowing and breathing out of the uterus.<\/p>\n

      \"Development
      Figure 16.2.5. Development of the embryonic disc<\/strong>. Formation of the embryonic disc leaves spaces on either side that develop into the amniotic cavity and the yolk sac.<\/figcaption><\/figure>\n

      On the ventral side of the embryonic disc, opposite the amnion, cells in the lower layer of the embryonic disk (the hypoblast<\/strong>) extend into the blastocyst cavity and form a yolk sac. The yolk sac supplies some nutrients absorbed from the trophoblast and provides primitive blood circulation to the developing embryo for the second and third week of development. When the placenta takes over nourishing the embryo at approximately week 4, the yolk sac has been greatly reduced in size and its main function is to serve as the source of blood cells and germ cells (cells that will give rise to gametes). During week 3, a finger-like out-pocketing of the yolk sac develops into the allantois, a primitive excretory duct of the embryo that will become part of the urinary bladder. Together, the stalks of the yolk sac and allantois establish the outer structure of the umbilical cord.<\/strong><\/p>\n

      The last of the extra-embryonic membranes is the chorion, which is the one membrane that surrounds all others. The development of the chorion will be discussed in more detail shortly, as it relates to the growth and development of the placenta.<\/p>\n

      Embryogenesis<\/h2>\n

      As the third week of development begins, the two-layered disc of cells becomes a three-layered disc through the process of gastrulation<\/strong>, during which the cells transition from totipotency to multipotency. The embryo, which takes the shape of an oval-shaped disc, forms an indentation called the primitive streak<\/strong> along the dorsal surface of the epiblast. A node at the caudal or \u201ctail\u201d end of the primitive streak emits growth factors that direct cells to multiply and migrate. Cells migrate toward and through the primitive streak and then move laterally to create two new layers of cells. The first layer is the endoderm<\/strong>, a sheet of cells that displaces the hypoblast and lies adjacent to the yolk sac. The second layer of cells fills in as the middle layer, or mesoderm<\/strong>. The cells of the epiblast that remain (not having migrated through the primitive streak) become the ectoderm<\/strong> (Figure 16.2.6).<\/p>\n

      \"Diagram
      Figure 16.2.6. Germ layers.<\/strong> Formation of the three primary germ layers occurs during the first 2 weeks of development. The embryo at this stage is only a few millimetres in length.<\/figcaption><\/figure>\n

      Each of these germ layers will develop into specific structures in the embryo. Whereas the ectoderm and endoderm form tightly connected epithelial sheets, the mesodermal cells are less organised and exist as a loosely connected cell community. The ectoderm gives rise to cell lineages that differentiate to become the central and peripheral nervous systems, sensory organs, epidermis, hair and nails. Mesodermal cells ultimately become the skeleton, muscles, connective tissue, heart, blood vessels and kidneys. The endoderm goes on to form the epithelial lining of the gastrointestinal tract, liver and pancreas, as well as the lungs (Figure 16.2.7).<\/p>\n

      \"Fates
      Figure 16.2.7. Fates of germ layers in embryo.<\/strong> Following gastrulation of the embryo in the third week, embryonic cells of the ectoderm, mesoderm, and endoderm begin to migrate and differentiate into the cell lineages that will give rise to mature organs and organ systems in the infant.<\/figcaption><\/figure>\n

      Development of the Placenta<\/h2>\n

      During the first several weeks of development, the cells of the endometrium\u2014referred to as decidual cells\u2014nourish the nascent embryo. During prenatal weeks 4\u201312, the developing placenta gradually takes over the role of feeding the embryo and the decidual cells are no longer needed. The mature placenta is composed of tissues derived from the embryo, as well as maternal tissues of the endometrium. The placenta connects to the conceptus via the umbilical cord, which carries deoxygenated blood and wastes from the foetus through two umbilical arteries; nutrients and oxygen are carried from the mother to the foetus through the single umbilical vein. The umbilical cord is surrounded by the amnion and the spaces within the cord around the blood vessels are filled with Wharton\u2019s jelly, a mucous connective tissue.<\/p>\n

      The maternal portion of the placenta develops from the deepest layer of the endometrium, the decidua basalis. To form the embryonic portion of the placenta, the syncytiotrophoblast and the underlying cells of the trophoblast (cytotrophoblast cells) begin to proliferate along with a layer of extraembryonic mesoderm cells. These form the chorionic membrane<\/strong>, which envelops the entire conceptus as the chorion. The chorionic membrane forms finger-like structures called chorionic villi<\/strong> that burrow into the endometrium like tree roots, making up the foetal portion of the placenta. The cytotrophoblast cells perforate the chorionic villi, burrow farther into the endometrium, and remodel maternal blood vessels to augment maternal blood flow surrounding the villi. Meanwhile, foetal mesenchymal cells derived from the mesoderm fill the villi and differentiate into blood vessels, including the three umbilical blood vessels that connect the embryo to the developing placenta (Figure 16.2.8).<\/p>\n

       <\/p>\n

      \"Cross-section
      Figure 16.2.8. Cross-section of the placenta.<\/strong> In the placenta, maternal and foetal blood components are conducted through the surface of the chorionic villi, but maternal and foetal bloodstreams never mix directly.<\/figcaption><\/figure>\n

      The placenta develops throughout the embryonic period and during the first several weeks of the foetal period; placentation<\/strong> is complete by weeks 14\u201316. As a fully developed organ, the placenta provides nutrition and excretion, respiration and endocrine function (Table 16.2.1 and Figure 16.2.9). It receives blood from the foetus through the umbilical arteries. Capillaries in the chorionic villi filter foetal wastes out of the blood and return clean, oxygenated blood to the foetus through the umbilical vein. Nutrients and oxygen are transferred from maternal blood surrounding the villi through the capillaries and into the foetal bloodstream. Some substances move across the placenta by simple diffusion. Oxygen, carbon dioxide, and any other lipid-soluble substances take this route. Other substances move across by facilitated diffusion. This includes water-soluble glucose. The foetus has a high demand for amino acids and iron, and those substances are moved across the placenta by active transport.<\/p>\n

      \"Photo
      Figure 16.2.9. Placenta.<\/strong> This post-expulsion placenta and umbilical cord (white) are viewed from the foetal side.<\/figcaption><\/figure>\n

      Maternal and foetal blood does not commingle because blood cells cannot move across the placenta. This separation prevents the mother\u2019s cytotoxic T cells from reaching and subsequently destroying the foetus, which bears \u201cnon-self\u201d antigens. Further, it ensures the foetal red blood cells do not enter the mother\u2019s circulation and trigger antibody development (if they carry \u201cnon-self\u201d antigens)\u2014at least until the final stages of pregnancy or birth. This is the reason that, even in the absence of preventive treatment, an Rh\u2212 mother doesn\u2019t develop antibodies that could cause haemolytic disease in her first Rh+ foetus.<\/p>\n

      Although blood cells are not exchanged, the chorionic villi provide ample surface area for the two-way exchange of substances between maternal and foetal blood. The rate of exchange increases throughout gestation as the villi become thinner and increasingly branched. The placenta is permeable to lipid-soluble fetotoxic substances: alcohol, nicotine, barbiturates, antibiotics, certain pathogens, and many other substances that can be dangerous or fatal to the developing embryo or foetus. For these reasons, pregnant women should avoid foetotoxic substances. Alcohol consumption by pregnant women, for example, can result in a range of abnormalities referred to as foetal alcohol spectrum disorders (FASD). These include organ and facial malformations, as well as cognitive and behavioural disorders.<\/p>\n

      Table 16.2.1<\/strong>. Functions of the placenta<\/p>\n\n\n\n\n\n\n
      Nutrition and digestion<\/strong><\/td>\nRespiration<\/strong><\/td>\nEndocrine function<\/strong><\/td>\n<\/tr>\n
      Mediates diffusion of maternal glucose, amino acids, fatty acids, vitamins and minerals<\/td>\nMediates maternal-to-foetal oxygen transport and foetal-to-maternal carbon dioxide transport<\/td>\nSecretes several hormones, including hCG, oestrogens and progesterone to maintain the pregnancy and stimulate maternal and foetal development<\/td>\n<\/tr>\n
      Stores nutrients during early to accommodate increased foetal demand later in pregnancy<\/td>\n<\/td>\nMediates the transmission of maternal hormones into foetal blood and vice versa<\/td>\n<\/tr>\n
      Excretes and filters foetal nitrogenous wastes into maternal blood<\/td>\n<\/td>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

      Organogenesis<\/h2>\n

      Following gastrulation, rudiments of the central nervous system develop from the ectoderm in the process of neurulation<\/strong> (Figure 16.2.10). Specialised neuroectodermal tissues along the length of the embryo thicken into the neural plate<\/strong>. During the fourth week, tissues on either side of the plate fold upward into a neural fold<\/strong>. The two folds converge to form the neural tube<\/strong>. The tube lies atop a rod-shaped, mesoderm-derived notochord<\/strong>, which eventually becomes the nucleus pulposus of intervertebral discs. Block-like structures called somites<\/strong> form on either side of the tube, eventually differentiating into the axial skeleton, skeletal muscle and dermis. During the fourth and fifth weeks, the anterior neural tube dilates and subdivides to form vesicles that will become the brain structures.<\/p>\n

      Folate, one of the B vitamins, is important to the healthy development of the neural tube. A deficiency of maternal folate in the first weeks of pregnancy can result in neural tube defects, including spina bifida\u2014a birth defect in which spinal tissue protrudes through the newborn\u2019s vertebral column which has failed to completely close. A more severe neural tube defect is anencephaly, a partial or complete absence of brain tissue.<\/p>\n

       <\/p>\n

      \"Diagram
      Figure 16.2.10. Neurulation.<\/strong> The embryonic process of neurulation establishes the rudiments of the future central nervous system and skeleton.<\/figcaption><\/figure>\n

      The embryo, which begins as a flat sheet of cells, begins to acquire a cylindrical shape through the process of embryonic folding<\/strong> (Figure 16.2.11). The embryo folds laterally and again at either end, forming a C-shape with distinct head and tail ends. The embryo envelops a portion of the yolk sac, which protrudes with the umbilical cord from what will become the abdomen. The folding essentially creates a tube, called the primitive gut, that is lined by the endoderm. The amniotic sac, which was sitting on top of the flat embryo, envelops the embryo as it folds.<\/p>\n

      \"Diagram
      Figure 16.2.11. Embryonic folding.<\/strong> Embryonic folding converts a flat sheet of cells into a hollow, tube-like structure.<\/figcaption><\/figure>\n

      Within the first eight weeks of gestation, a developing embryo establishes the rudimentary structures of all its organs and tissues from the ectoderm, mesoderm and endoderm. This process is called organogenesis.<\/strong><\/p>\n

      \"Embryo
      Figure 16.2.12. Embryo at seven weeks.<\/strong> An embryo at the end of seven weeks of development is only 10 mm in length, but its developing eyes, limb buds, and tail are already visible. (This embryo was derived from an ectopic pregnancy.) (credit: Ed Uthman).<\/figcaption><\/figure>\n

      Like the central nervous system, the heart also begins its development in the embryo as a tube-like structure, connected via capillaries to the chorionic villi. Cells of the primitive tube-shaped heart are capable of electrical conduction and contraction. The heart begins beating in the beginning of the fourth week, although it does not actually pump embryonic blood until a week later, when the oversized liver has begun producing red blood cells. (This is a temporary responsibility of the embryonic liver that the bone marrow will assume during foetal development.) During weeks four\u2013five, the eye pits form, limb buds become apparent and the rudiments of the pulmonary system are formed.<\/p>\n

      During the sixth week, uncontrolled foetal limb movements begin to occur. The gastrointestinal system develops too rapidly for the embryonic abdomen to accommodate it and the intestines temporarily loop into the umbilical cord. Paddle-shaped hands and feet develop fingers and toes by the process of apoptosis (programmed cell death), which causes the tissues between the fingers to disintegrate. By week seven, the facial structure is more complex and includes nostrils, outer ears and lenses (Figure 16.2.12). By the eighth week, the head is nearly as large as the rest of the embryo\u2019s body and all major brain structures are in place. The external genitalia are apparent, but at this point, male and female embryos are indistinguishable. Bone begins to replace cartilage in the embryonic skeleton through the process of ossification. By the end of the embryonic period, the embryo is approximately three cm from crown to rump and weighs approximately eight grams.<\/p>\n

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      Section Review<\/strong><\/p>\n<\/header>\n

      \n

      As the zygote travels toward the uterus, it undergoes numerous cleavages in which the number of cells doubles (blastomeres). Upon reaching the uterus, the conceptus has become a tightly packed sphere of cells called the morula, which then forms into a blastocyst consisting of an inner cell mass within a fluid-filled cavity surrounded by trophoblasts. The blastocyst implants in the uterine wall, the trophoblasts fuse to form a syncytiotrophoblast, and the conceptus is enveloped by the endometrium. Four embryonic membranes form to support the growing embryo: the amnion, the yolk sac, the allantois and the chorion. The chorionic villi of the chorion extend into the endometrium to form the foetal portion of the placenta. The placenta supplies the growing embryo with oxygen and nutrients; it also removes carbon dioxide and other metabolic wastes.<\/p>\n

      Following implantation, embryonic cells undergo gastrulation, in which they differentiate and separate into an embryonic disc and establish three primary germ layers (the endoderm, mesoderm and ectoderm). Through the process of embryonic folding, the foetus begins to take shape. Neurulation starts the process of the development of structures of the central nervous system and organogenesis establishes the basic plan for all organ systems.<\/p>\n<\/div>\n<\/div>\n

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      Review Questions<\/strong><\/p>\n<\/header>\n

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