Embryonic growth depends directly on mitosis. Through this type of cell division, the zygote divides, producing a series of cells that also compose differentiated tissues and organs via mitosis until the formation of a complete individual.
Vitellus (yolk) is the nutritive material that accumulates in the cytoplasm of the egg (zygote), and has the function of nourishing the embryo. Depending on the amount of vitellus in them, vertebrate eggs are classified as oligolecithal (little yolk), centrolecithal, or heterolecithal (more yolk diffusely distributed) and telolecithal (more yolk concentrated at one end of the egg).
The animal pole of a telolecithal egg is the portion of the egg with little vitellus. It is opposite to the vegetal pole, which is the region where the yolk is concentrated.
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The four initial stages of embryonic development are the morula stage, the blastula stage, the gastrula stage and the neurula stage.
Cell division during the first stage of embryonic developments is called cleavage, or segmentation. During this stage, several mitoses occur within the zygote to form the new embryo.
The cells that are produced during cleavage (the first stage of embryonic development) are called blastomeres. In this stage the embryo is called the morula (similar to a “morus”, or mulberry).
After passing the morula stage in which the embryo is a compact mass of cells, the next stage is the blastula stage. In the blastula stage, the compactness is lost and an internal cavity filled with fluid appears inside it, called the blastocele.
The blastula turns into the gastrula through a process known as gastrulation.
Gastrulation is the process through which a portion of the blastula wall invaginates inside the blastocele, forming a tube called the archenteron (a primitive intestine). The cells of the inner side of the tube form the endoderm (a germ layer) and the cells of the outer side form the ectoderm (another germ layer). This is the beginning of tissue differentiation in embryonic development.
The archenteron is the tube formed during gastrulation by means of the invagination of the blastula wall inside the blastocoel. It turns into the gastrointestinal tract. The blastopore is archenteron's exterior opening . The blastopore produces one of the extremities of the digestive tract: the mouth in protostome organisms, or the anus in deuterostome organisms.
The mesoderm is formed through the differentiation of the endodermal cells that cover the dorsal region of the archenteron.
The three germ layers are the ectoderm, the mesoderm and the endoderm.
Cnidarians are diploblastic, meaning that they only have an endoderm and ectoderm. With the exception of poriferans, all remaining animals are triploblastic. Poriferans do not have differentiated tissue organization and, as a result, have no classification regarding germ layers (although sometimes they are considered diploblastic).
The neurula stage is characterized by the appearance of the neural tube along the dorsal region of the embryo. The growth of the mesoderm in that region causes the differentiation of the ectodermal cells just above it. These cells then differentiate to form the neural tube. Therefore, the origin of the nervous system is the ectoderm (the same germ layer that produces the skin).
The notochord is a rodlike structure that forms the supporting axis of the embryo and which produces the spine in vertebrates. It is formed through the differentiation of mesodermal cells.
Coeloms are cavities delimited by a mesoderm. Coeloms turn into cavities where the internal organs of the body are located, such as the pericardial cavity, the peritoneal cavity and the pleural cavity.
In addition to coelomate animals, there are also acoelomate animals, such as platyhelminthes, and pseudocoelomate animals, such as nematodes.
Coeloms are produced from the mesoderm.
The pleura is the membrane that covers the lungs and the inner wall of the chest; the pericardium is the membrane that covers the heart; and the peritoneum is the membrane that covers most organs of the gastrointestinal tract and part of the abdominal cavity. All these membranes surround coeloms (internal cavities).
In a schematic longitudinal section of an embryo after the neurula stage, the outermost layer of cells is the ectoderm. In the ventral region, the archenteron tube is formed of endodermal cells. In both sides of the embryo, coeloms covered by a mesoderm are present. In the central region above the archenteron and in the middle of the coeloms, the notochord is located. In the dorsal region just above the notochord, the neural tube is located.
Somites are differentiated portions of mesodermal tissue which are longitudinally distributed along the embryo. Somites turn into muscle tissue and portions of connective tissues.
Histogenesis is the process of tissue formation during the embryonic development. Organogenesis is the process of organ formation. Before histogenesis and organogenesis, primitive embryonic structures have been already formed: germ layers, the neural tube, the notochord, coeloms, and somites.
The epidermis and the nervous system have the same embryonic origin: the ectoderm. Epidermal appendages (such as nails, hair, sweat glands and sebaceous glands), the mammary glands, the adenohypophysis, the cornea, the crystalline lens and the retina are also produced from the ectoderm.
Blood cells have a mesodermal embryonic origin. Other organs made from the mesoderm are: serous membrane coverings such as the pericardium, the peritoneum and the pleura, muscles, cartilage, the dermis, adipose tissue, the kidneys, the ureters, the bladder, the urethra, the gonads, blood and lymph vessels, and bones.
The liver and the pancreas are produced from the endoderm. Also of endodermal origin are the epithelium of the airway, the epithelium of the bladder, the epithelium of the urethra and the epithelium of the GI tract (except for the mouth and anus), the alveolar cells of the lungs and the thyroid and parathyroid glands.
Twins are simultaneously generated (within the mother’s uterus) offspring. Twins are classified according to zygosity as monozygotic or dizygotic twins.
Monozygotic twins, also known as identical twins, are those that originate from one single fertilized ovum (therefore from one single zygote); monozygotic twins are genetically identical, meaning that they have identical genotypes and are necessarily of the same sex. Dizygotic twins, also known as fraternal twins, are those generated from two different ova fertilized by two different sperm cells; therefore, they are not genetically identical and they are not necessarily of the same sex.
Polyembryony is the phenomenon in which a single embryo in its initial embryonic stage divides itself to form many new individuals of the same sex and who are genetically identical. This is the way, for example, in which reproduction takes place in armadillos of the genus Dasypus. Polyembryony is an example of natural “cloning”.
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