THE CONCEPTS AND LANGUAGE OF DEVELOPMENT Flashcards

1
Q

Define Embryology

A

Embryology is the branch of medicine concerned with the study of embryos and their development

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2
Q

What is the first stage in the development of a foetus?

A

The process of the egg and sperm coming together.

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3
Q

Identify 4 key features of a fertilised egg

A

There are a few identifiable features of the fertilised oocyte:

Zona Pellucida (Bright ring) – this is glycoprotein material
Within the zona pellucida is the zygote with two pronuclei (with one haploid nucleus from the male and female respectively). They are yet to fuse.
The perivitelline space – a fluid filled space that surrounds the embryo
Polar bodies in the perivitelline space (either one or two bodies)

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4
Q

Where do polar bodies come from?

A

They contain a portion of female genetic material. Females generate all of their germ cells prior to birth, where they form one oocyte.

A germ cell will duplicate its nuclear DNA, they briefly enter meiosis but then arrest after prophase 1 and will remain in this state into adult life.
When a single oocyte is chosen it will then finish meiosis.
Once meiosis continues the first meiotic division occurs to produce two cells that are unequal. Half of the genetic material is extruded into a polar body which will be found in the perivitelline body (the first polar body).
The selected oocytes will arrest in metaphase 2
In order for meiosis to now resume the oocyte must be fertilised.
Second meiotic division then occurs and another polar body will be extruded

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5
Q

Learn the summary diagram of when events occur during embryology

A

On image

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6
Q

What is cleavage and describe the phases of it?

A

Cleavage stages (process of splitting into two cells without growth)

The pronuclei first fuse and the zygote will under mitosis.
Approximately thirty hours after fertilisation, the oocyte splits into two cells of equal size called blastomeres.
This will produce 2 cells and divide again to give 4 cells
All of this is contained in the zona pellucida, so the cells are getting smaller

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7
Q

Describe how the blastocyst will form the morula and attachment to the endometrium of the uterus

A

After 3 more divisions, there are 12-16 cells. At this point, the group of cells is referred to as the morula. They have divided asyncrhonly and are all loosely attached to each other.
It will then undergo compaction where the cells on the outer part of the embryo will become flatter and form an epithelial barrier (with cell junctions between).
This allows for fluid to enter the central region of the embryo which is called the blastocoel and the embryo is now called a blastocyst. It consists of two cell types:
a. Outer cell mass (trophoblast) – contacts with the endometrium of the uterus to facilitate implantation and the formation of the placenta. Inner cell mass (embryoblast) – responsible for the formation of the embryo itself.
N.B this is happening in the oviduct and anything after cleavage is called blastulation
This zona pellucida will then be dissolved by secretory enzymes from the embryo, the blastocyst will then hatch out around 6/7 days. This degrades the protein coat, the blastocyte then hatches out.
The trophoblasts have also differentiated to allow the blastocyst to implant into the uterine wall.
During the second week, the trophoblast and embryoblast divide into increasingly specialised cell types. The trophoblast divides into the syncytiotrophoblast and cytotrophoblast. The embryoblast divides into the epiblast and hypoblast, forming a two-layered structure; the bilaminar disk. The amniotic cavity forms within the epiblast.

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8
Q

Describe the process of implantation

A

After the initial rounds of cellular divisions, the embryo must implant into the endometrium of the uterus.

During this process, the syncytiotrophoblast becomes continuous with the uterus – such that maternal blood vessels (known as sinusoids) invade the spaces within the syncytiotrophoblast (known as lacunae). At this point, uteroplacental circulation has begun; and further embryonic development can occur.

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9
Q

What makes up the bilaminar germ disk?

A

The cells of the inner cell mass have also started to proliferate which have formed a bilaminar germ disk (a two layered embryonic disk). This consists of the epiblast cells and hypoblast cells.

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10
Q

Summarise gastrulation

A

During the 3rd week of embryonic development, the cells of the bilaminar disk (epiblast and hypoblast) undergo a specialised process called gastrulation. During this time, the two cell layers become three germ layers and the bodily axes observed in the mature adult are created.

It is a process of cellular rearrangement involving migration, invagination and differentiation of the epiblast, largely orchestrated by the primitive streak. This is a groove in the midline of the epiblast which appears during the third week. Within the primitive streak lies a primitive node at the cranial end, and within the primitive node lies the primitive pit.

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11
Q

Gastrulation – what happens to the bilaminar germ disk?

A

Cells of the epiblast layer break off and migrate toward the primitive pit. Here, they detach and penetrate through the epiblast layer to form three new germ cell layers:

Endoderm – formed by epiblast cells that migrate through the primitive pit and displace the hypoblast cells. (Lower)
Mesoderm – formed by epiblast cells that migrate through the primitive pit and lie between the epiblast layer and the newly created endoderm. (middle)
Ectoderm – formed by the epiblast cells that remain in position. (Top)

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12
Q

What will the bilaminar germ disk form?

A

The epiblast cells will then differentiate into endoderm cells which will then replace the hypoblast layer.

Epiblast cells also forms the mesoderm. Epiblast cells will ingress and involute to form a 3 layered embryo

On the top is ectoderm (cells from the epiblast that didn’t differentiate)

Cells of the bilaminar germ disk will migrate anteriorly, posteriorly and laterally to form other tissues. These are shown by the arrows on the epiblast

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13
Q

What is Hensons node?

A

Hensons node is where gastrulation is being initiated and acts as a signalling centre by secreting growth factors that cause changes to the surrounding cells

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14
Q

Summarise neurulation

A

In the mesoderm we have a further differentiation of cells in the middle to form a chord known as notochord (beneath of the primitive streak). Its purpose is mainly in neurulation

It induces a thickening change in the ectoderm above it called the neural plate

The neural plate forms a tube and zips up it forms the neural tube, cells also invade the mesoderm from the ectoderm known as neural crest cells.

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15
Q

Describe what can be seen at day 16 and 20

A

Day 16 – the embryo will continue to divide and fold, lots of proliferation is going on but differs between tissues. This shows a sagittal section through the embryo: we have the cranial and caudal on the left and right. It is folding towards the midline from both ends.

On the transverse section we can also see lateral folding.

Folding brings the heart tissue inwards,
Endoderm will form the lining of the gut
Here we looking at a top-down view of the embryo with cranial towards the top and caudal towards the bottom.

The pink structure is a developing nervous system, this sheet of cells will role to form the neural tube and then fuse.

At day 22 the part of the neural tube has fused together to meet in the middle.
In a cross section we have somites

The grey is the notochord ventral to the neural tube

Remember the anterior and posterior neuropore are exposed due to closure of the neural tube

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16
Q

Describe the cloth purse model

What membranes close the cranial and caudal ends?

What forms the umbilical cord?

Where does the septum and the heart move?

Describe the planes

A

Folding to bring organs where they should be
Closed at the cranial end by the oral pharyngeal membrane and posterior by the cloacal membrane
* This process of folding is called embryonic folding
* It occurs in two planes, the horizontal plane and the median plane
* Folding in the horizontal plane results in two lateral body folds
* Folding the median plane results in the development of cranial and caudal fold
* The endoderm will move towards the midline and fuse to form the primitive gut tube which will differentiate into three main parts, the foregut, midgut and hindgut (caudal end)

17
Q

What are the results of folding?

A

Folding forms the endodermal gut tube

Formation of the umbilical cord

18
Q

Summarise the structures derived from the endoderm, mesoderm and ectoderm

A

On table

19
Q

Changes in cell fate are accompanied by molecular changes
* How are these controlled?

A
  • Option 1 – Mosaic development (cell autonomous specification) – information for what the cell will become is inherited and is contained in the cell
    o Information inherited from parental cell
  • Option 2 – Regulative development (conditional specification) – the cell can become a variety of cell types depending on the environment
    o Cell influenced by its surroundings, or position, within the embryo
20
Q

What does Weismann’s nuclear determinants show?

A
  • This image shows that after each cleavage each cell has inherited a different nuclear factor or determinant. This follows on from option 1 of mosaic development whereby factors are inherited.
21
Q

Describe Roux’s experiments on determination

A

Roux’s attempt to show mosaic development. Destroying (but not removing) one cell of a 2-cell frog embryo results in the development of only one-half of the embryo.
This is mosaic development – during stage two the embryo has inherited different factors forming a left and right side of a frog embryo. However this conclusion is wrong. This dead half is impeding with the regulation of the live right side.
Tying a not round the 2-cell embryo and separating them results in the formation of two embryos each with a left and right embryo
It would seem like mosaic development – BUT THIS IS WRONG!

22
Q

Why is C. elegans development mosaic?

A

This is mosaic development, it is early hatched and what cell types represent. Differentiation and specific cell fates can be traced back to their origins.

22
Q

Describe:

Driesch’s separation of sea urchin blastomeres demonstrates regulative development

A

Driesch’s demonstration of regulative development. (A) An intact 4-cell sea urchin embryo generates a normal pluteus larva. (B) When one removes the 4-cell embryo from its fertilization envelope and isolates each of the four cells, each cell can form a smaller, but normal, pluteus larva. (All larvae are drawn to the same scale.) Note that the four larvae derived in this way are not identical, despite their ability to generate all the necessary cell types. Such variations are also seen in adult sea urchins formed in this way (Marcus 1979).
Each cell is fully capable of forming all the cell types of the pluteus larva (shown in diagram above on right)

23
Q
A