Developmental biology 2 (Prof. Dale) Flashcards

1
Q

How is the yolk distributed in sea urchin eggs ?

A

Evenly.

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2
Q

What are micromeres in the sea urchin egg ?

A

Micromeres = small blastomeres produced at the vegetal pole.

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3
Q

What is the structure of the blastula generated by the sea urchin egg ?

A

At the 62-cell stage, the blastula consists of a simple epithelium surrounding a fluid filled blastocoel.

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4
Q

How does gastrulation take place in the sea urchin embryo ?

A
  • vegetal pole of the sea urchin blastula thickens to form a the vegetal plate –> releases primary mesenchyme cells into the blastocoel
  • vegetal plate buckles inwards to form the archenteron + a group of secondary mesenchyme cells form at the tip –> these cells produce pseudopodia that attach to the animal pole + pull the archenteron towards it
  • archenteron fuses with the animal pole to form a continuous tube (the gut) with the blastopore forming the anus
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5
Q

What causes the buckling of the vegetal plate in the sea urchin embryo ?

A

It is caused by localised contraction of actin-myosin microfilaments near the apical surface of the blastula epithelium –> apical contraction narrows the apical surface relative to the basal surface, bending the epithelium inwards

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6
Q

What is invagination in the see urchin embryo ?

A

Invagination = inward movement of cells at the vegetal pole following apical contraction

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7
Q

How is elongation of the archentron mediated in the sea urchin embryo ?
What is the combined effect on the archentron in this process ?

A

By convergent-extension, in which cells acquire lamellipodia (made of β-actin) perpendicular to the invaginating vegetal plate and intercalate with each other.
This narrows the archenteron (convergence) + at the same time elongates it (extension).

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8
Q

What are the different steps of cleavage divisions in mammalian embryos ?

A
  • mitosis = initiated ~ 24 hours after fertilisation + occurs every 12-24 hours
  • at the morula stage (~16 cells) they cells undergo compaction (maximize their contacts)
  • cells at the centre = inner cell mass (ICM)
  • peripheral cells = the trophoblast
  • blastocoel cavity that forms in the centre of the embryo (now called the blastocyst)
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9
Q

What are the different fates in the mammalian blastocyst ?

Does this vary between animal kingdoms (phyla) ?

A
  • trophoblast –> forms the chorion (placenta)
  • the ICM –> divides into epiblast + hypoblast layers
  • hypoblast –> differentiates as extraembryonic endoderm
  • epiblast –> forms the amniotic membrane, extraembryonic mesoderm + all tissues (ectoderm, mesoderm and endoderm) of the fetus
    Each germ layer forms similar tissues in all animal phyla.
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10
Q

To which tissue types does the ectoderm give rise to ?

A

Epidermis + nervous system (cartilage/bone in the head)

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11
Q

To which tissue types does the mesoderm give rise to ?

A

Cartilage/bone, connective tissue muscle, kidney, blood, vasculature, heart + gonads

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12
Q

To which tissue types does the endoderm give rise to ?

A

Digestive tract (epithelium), lungs, liver, gall bladder + pancreas

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13
Q

How does implantation take place ?

What happens to the ICM ?

A
  • mammalian blastocyst attaches to uterine wall + trophoblast proliferates to form syncytiotrophoblast = highly invasive tissue that penetrates the uterine wall
  • formation of lacunae that will fill with maternal blood from uterine capillaries
  • ICM divides into epiblast + hypoblast layers
  • epiblast –> forms the amniotic membrane
  • hypoblast –> forms Heuser’s membrane
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14
Q

What is ingression and when does it happen ?

A

Ingression = process where epiblast cells migrate through the primitive streak and node as individual cells, happens during gastrulation

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15
Q

What are the different stages of gastrulation ?

A
  • ingression
  • the 1st cells to ingress invade + displace the hypoblast –> forming embryonic endoderm
  • subsequent cells migrate into the space between the epiblast / endoderm –> forming the mesoderm
  • cells remaining in the epiblast layer form ectoderm
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16
Q

What are the 5 types of mesoderm ?

How are these and the notochord formed ?

A
  • cells migrating through the node = axial mesoderm + prechordal mesoderm + notochord
  • mesoderm from primitive streak condenses either side of the notochord = paraxial mesoderm, intermediate mesoderm + lateral plate mesoderm
17
Q

How are somites formed and along which axis ?
What are they made of ?
How many are formed ?

A
  • paraxial mesoderm –> forms pairs of somites, sequentially from rostral to caudal
  • the number formed varies between species
  • somites = formed of a simple epithelium surrounding a central cavity
18
Q

What do somites subsequently divide into ?

A

In response to signals from surrounding tissues, they subsequently divide into sclerotome, myotome and dermatome layers.

19
Q

How is the lateral-plate mesoderm further subdivided ?

A
  • Sometopleuric (most lateral)

- Splanchnopleuric (more medial)

20
Q

To what organs/tissues do the mesodermal tissues give rise to ?

A
  • Dermatome: dermal (deep) layer of skin
  • Myotome: skeletal (striated) muscle
  • Sclerotome: vertebrae, ribs, sacrum, coccyx
  • Intermediate: kidneys, gonads, reproductive tracts
  • Somatopleuric: limb bone, connective tissues, vasculature, blood
  • Splanchnopleuric: cardiac mesoderm, smooth muscle,
    connective tissues, vasculature, blood
21
Q

What is the neural plate ?

From what does it form ?

A
  • the neural plate = precursor of the NS

- the ectoderm anterior to node forms the neural plate

22
Q

What is the fate of neural plate cells compared to epidermal cells ?

A
  • cells of the neural plate –> elongate to form a
    pseudostratified columnar epithelium
  • cells of the epidermis –> remain cuboidal
23
Q

What is regression ?

A

Regression = a phenomenon where, as the embryo
expands through cell proliferation, the primitive streak
becomes restricted to the posterior margin of the epiblast

24
Q

When does the neural tube form ?

A

4th week of human development.

25
Q

How does the neural tube close ?

Which parts of the tube close last ?

A
  • the edges initially meet at only a single site –> at the boundary of the hindbrain and spinal cord (but in reality there may also be a sites in the midbrain and at the anterior boundary)
  • the rest of the tube closes like a “zipper” from the initial sites, the caudal neuropore closing last
26
Q

What drives neural tube closure ?

A
  • cell shape changes drive neural tube closure
  • prior to neurulation, neuroepithelial cells = cuboidal
  • during neurulation –> cells elongate along apical-basal axis to become columnar
27
Q

What forces neuroectodermal cells to adopt a wedge shape ?

A

Apical constriction –> occurs when the apical actin-myosin cable contracts, forcing cells to adopt wedge shape. This generates the physical force that causes the neural plate to bend.

28
Q

What are hinge points ?

A

Hinge point = apical contraction sites causing neural plate to bend

29
Q

What are the most common neural tube defects (NTDs) ?
How frequent are they ?
How lethal are they ?

A
  • Anencephaly = rostral neuropore fails to close
  • Spina bifida when caudal neuropore fails to close.
  • Anencephaly + spina bifida account for up to 95% of all NTD, with equal prevalence
  • affects ~1400 UK/year, 90% are terminated
30
Q

Where are neural crest cells formed ?

A
  • neural crest cells –> formed at the lateral edges of the neural plate –> become the roof of the neural tube
  • they delaminate from the neural tube to become a mesenchymal population that migrates away form the neural tube to form many different cell types
31
Q

Which cells will mesodermal neural crest cells give rise to ?

A
  • smooth muscle
  • osteoblasts
  • osteoclasts
  • adipocytes
  • chondrocytes
32
Q

Which cells will ectodermal neural crest cells give rise to ?

A
  • melanocytes
  • Schwann cells
  • PNS neurons
33
Q

In which species is the neural crest found ?

Why is this important ?

A

In vertebreate embryos.

Considered crucial for vertebrate evolution.

34
Q

At what point do mammalian embryos display the basic vertebrate body plan ?
Which organs can we thus see ?

A
  • at the end of neurulation
  • we can make out the forebrain (fb), midbrain (mb), hindbrain (hb), trunk (t), a large heart (h), aorta, and umbilical cord
35
Q

What is the phylotypic stage ?

What happens after this stage ?

A
  • Phylotypic stage = the point where vertebrate embryos are most similar to each other at the end of neurulation and share a common body plan
  • After –> morphology increasingly diverges
36
Q

What evidence supports that, at the phylotypic stage, vertebrate embryos share the same “molecular anatomy”

A

Using in situ hybridization, we can see that the mRNA of a gene called krox-20 is localised to two stripes in the hindbrain of mouse, chick, frog, and fish embryos.

37
Q

By which point are most of the organs formed in human embryos ?
When do all these organs become functional ?

A
  • most of the organs are formed during a 4 week period after the formation of the body plan = organogenesis
  • most of the organs and tissues –> become fully functional during the fetal period (~30 weeks)
  • even then only a very immature infant is born