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Lecture notes

Mechanisms of Disease During Embryogenesis

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Exploring the different causes underlying birth defects.

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Mechanisms of Disease During Embryogenesis

Learning Objectives:
 Have an appreciation of the complexity involved in embryonic development
 Understand the difference between genetic and environmental causes for congenital
disease
 Be able to identify examples of birth defects and relate them to a specific
developmental process

2 main periods of human development
 Embryonic period: until end of week 8 where most of organogenesis occurs
 Fetal period: remaining time in utero, involves growth and modelling

Mechanisms of development (order)
Egg → fertilisation → cleavage → gastrulation → neurulation and somitogenesis →
organogenesis → adult

Overview of Developmental Stages
 Day 1: Fertilised zygote which is surrounded by a thick protective membrane called
the zona pellucida
o 2 polar bodies are also produced due to the unequal cell division after a
secondary oocyte divides. So 1 set of chromosomes are pulled aside and form
the first polar body.
 Cleavage stages: Fertilised egg moves along uterine tube and divides as it goes along
(1 cell zygote → 2 cell zygote → 4 cell zygote → 8 cell zygote)
 Day 3: 16 cell zygote then forms the Morula. The zona pellucida then starts to
dissolve or is shed off the Morula slowly.
 Day 4/5: Morula turns into a Blastocyst (32 cells) - this still has the zona pellucida.
They then implant onto the uterine wall (in order to derive nutrition).
o Deriving nutrition, giving away wastes & exchanging gases can be served
through a barrier = this barrier is an organ called the placenta.
 Day 6/7: The blastocyst develops a cystic cavity called a blastocele. This contains a
trophoblast cell layer.
o Trophoblast cell layer are cells that form the outer layer of a blastocyst. They
provide nutrients to the embryo & develop into a large part of the placenta.

Gastrulation
 Transformation of bilaminar disc (epiblast and hypoblast) → into trilaminar disc
(ectoderm, mesoderm & endoderm)
 Hypoblast layer becomes displaced by involuting cells that later form mesoderm &
endoderm
Ectoderm (outer layer)
 Epiblast layer → Ectoderm layer → Skin, Nervous Systems & Pituitary
Mesoderm (middle layer)
 In the middle of Epiblast and Hypoblast layer → Mesoderm layer → MSK, CVS, Repro
systems & Connective Tissue
Endoderm (inner layer)

Document information

Uploaded on
June 16, 2021
Number of pages
2
Written in
2020/2021
Type
Lecture notes
Professor(s)
Dr florencia cavodeassi
Contains
All classes
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