Embryology 2 Flashcards
What is the primitive streak?
Formed in the midline of the epiblast, by the invagination of cells.
Once formed, the axis of the embryo forms.
What is gastrulation?
The formation of three germ layers.
The ectoderm, mesoderm and endoderm.
What causes gastrulation?
When epiblast cells migrate to lie between the epiblast and hypoblast layers.
Hypoblast cells are displaced.
What does gastrulation form?
A trilaminar disc.
The cells have now become specialised.
How are notochords formed?
A primitive streak forms in the ectoderm.
Cells sink to form a solid tube.
A notochord (a solid tube of cells) form below the mesoderm.
What is neurulation?
A neural plate forms in the ectoderm.
It sinks down to form a neural tube.
The notochord induces ectodermal cells in the midline to form a neural tube.
What does the mesoderm separate into?
The neural tube induces the mesoderm to thicken and separate into the paraxial mesoderm, intermediate plate mesoderm, and lateral plate mesoderm.
What does the lateral plate mesoderm split into?
Somatic mesoderm.
Splanchnic mesoderm.
The intra-embryonic coelom is the space between.
What are somites?
Formed by the segmentation of the paraxial mesoderm.
Each somite divides into the dermatome (dermis of the skin), myotome (muscles) and sclerotome (bones).
What does the ectoderm develop into?
Neural tube - forebrain, midbrain, hindbrain, and spinal cord.
Epidermis of the skin.
What do the layers of the mesoderm develop into?
Paraxial - 43 pairs of somites.
Intermediate - urogenital system.
Lateral plate - body cavities and pleura.
What does the lateral plate mesoderm split into?
Somatic mesoderm.
Splanchnic mesoderm.
Intra-embryonic coelom (the space between).
What does the endoderm form?
The gut.
The respiratory system.
What are teratogens? Give examples.
Environmental factors that cause abnormal development.
Drugs, alcohol, tobacco, infectious agents that can transfer through the placenta, and radiation.
Describe the levels of sensitivity to teratogens during embryonic growth.
Weeks 1-2 - high risk of death, low risk from teratogens.
Weeks 3-8 - period of greatest sensitivity to teratogens.
Weeks 9-38 - decreasing sensitivity.