Embrology 2 Flashcards

1
Q

When is the embryonic development period?

A

Weeks 3-8 (inclusive) of a pregnancy

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2
Q

What are some key features of the embryonic period?

A

The period of greatest change
All major structures and systems formed
Greatest risk of major congenital malformation - due to environ exposure or drugs

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3
Q

How does drug therapy effect a growing baby through the difff stages of development?

A

In pre-embryonic stage- lethal effects- loose pregnancy

In embryonic stage- very sensitive-significant/catastrophic effect

In feral stage- less sensitive but can still cause damage

After embryonic period risk of a structure defect is lowered except for CNS which is still very sensitive to alcohol etc

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4
Q

What is the result of early embryonic development and what does this involve?

A

Result= foundations laid for development of body systems

Means sufficient cell number of the right type in the right place

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5
Q

List the key events/processes in early development. Why is each stage so key to the next?

A
Fertilisation & implantation 
Gastrulation
Neurulation 
Segmentation 
Folding

All so key ad each step depends on the preceding step being completed successfully

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6
Q

What marks the start of gastrulation?

A

At the end of the 2nd week the epiblast is a uniform disk. After Gastrolation a new feature the “primitive streak” appears on the dorsal surface of the epiblast

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7
Q

What happens during gastrulation?

A

Cells in the epiblast layer divide and migrate upwards into the epiblast layer. The hypoblast is displaced and a 3rd layer is created.

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8
Q

What is the structure created after gastrulation?

A

A triluminar disc made up of an ectoderm (becomes outside of foetus), a mesoderm (is middle), and an endoderm (becomes inside of foetus).
All 3 are derived from the epiblast layer.

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9
Q

What does the ectoderm go on to become?

A

The organs and structures that maintain contact with the outside world

Eg nervous system, skins epidermis

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10
Q

What does the Mesoderm go on to form?

A

Supporting tissues

Eg muscle, cartilage, bone and vascular system (inc heart and vessels)

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11
Q

What does the endoderm go on to form?

A

The internal structures

Eg GI tract’s epithelial lining, respiratory tract and parenchyma of glands

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12
Q

What is situs inverses? What are the complications if any?

A

It’s when the viscera is a complete mirror image of what it should be.
Commonly results from immobile cilia spring embryogenesis
No usual associated morbidity
Problems arise if there is both normal and mirror-image present

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13
Q

How is left-right asymmetry achieved?

A

On the node of the streak there are cilated cells. The action of these results in left-ward flow of signalling molecules. This causes side-specific signalling to cascade.

IE on left hand side any signalling molecules arrive
Lack of signals on right side is a signal within itself

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14
Q

Summarise when, what, how and why for Gastrulation.

A

When-3rd wee of development (starts embryonic period)

What-bilaminar disk becomes trilaminar disk with 3 germ layers

How-primitive streak forms leading to migration & invagination of cells

Why-to ensure correct placement or precursor tissues to allow subsequent morph oh genesis to take place

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15
Q

What is a Notochord?

A

A solid rod of cells running in the midline with an key signaling role.

It directs conversion of overlying ectoderm to Neuroectoderm.

(Receptors for this on ectoderm only not endoderm)

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16
Q

How is the neural tube formed?

A

Notochord signals cause the overlaying ectoderm to thicken
Becomes a slipper shaped neural plate

The edges elevate out of the plane of the disk and curl towards each other. This creates the neural tube.

17
Q

Once the neural tube has formed what happens to the mesoderm?

A

It forms 4 separate parts.
2 shelf like parts = somatic mesoderm (forms the body) and the splachnic mesoderm (forms the viscera)
The mesoderm inbetween these 2 is called the intraembryonic mesoderm
The mesoderm surrounding the neural tube is called the paraxial mesoderm

18
Q

What is a somite and what can it be used for?

A

It a segment of the paraxial mesoderm.
Leave a total of 31
They appear at highly regular intervals and are predictable so allow us to age an embryo accurately

19
Q

What is the organised degeneration of somites?

A

Originally appear as a regular block of mesoderm cells around a cavity.
They then degenerate (Ventral wall breaks down, formation of the sclerotium)
Then further organisation of dorsal portion forms the combined dermomyotome.
The myotome proliferates and migrates, dermatologists disperses.

20
Q

What can be derived from a somite?

A

Dermatome-skin section -“dermis”
Myotome-muscle section-muscles
Sclerotme-hard tissue section-bones

21
Q

Why is the final number of somites important and what is it?

A

31 is the key number. Also the number of pairs of spinal nerves.

22
Q

What happens to the triluminar disk after the neural tube is formed?

A

It begins to fold so that the outside is covered entirely by ectoderm, and the endoderm is fully inside (other than a small hole to access yolk).
This begins with cephalocaudal folding (head and tail fold) then lateral folding (sides fold).
The entire embryo is then enveloped in the amniotic sac.

23
Q

During folding what does the yolk help form?

A

The intraembryonic cavity.

24
Q

What is folding designed to achieve?

A

Draws the margins of the disc together
Creates a ventral body wall
Pulls amniotic membrane around disc-suspends embryo
Pulls connective stalk centrally