l1 Flashcards

1
Q

what is the neural plate?

A

single cell thick neuroepithelium which is induced by ectoderm on dorsal side of embryo (BMP antagonists)

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2
Q

where does the neural plate sit?

A

sits above mesoderm and endoderm
- grows and elongates along AP axis then roles into neural tube (neuralation)
(above prechordal mesoderm/notochord)

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3
Q

how do neural plate cells form?

A

via DIFFERENTIATION

- cells become different to one another and aquire specialised properties which are caused by changes in gene expression

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4
Q

what is gene expression governed by?

A

both extrinsic factors (morphogens) and instrinsic factors (TFs)

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5
Q

give the two fates of an ectoderm determined by BMP

A
  • BMP antagonism - neural plate cell

- BMP agonism - epidermal cell

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6
Q

What TFs does the spemann organiser release?

A
  • BMP ANTAGONISTS
  • noggin
  • chordin
  • gsc
  • follastatin
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7
Q

where is the neural plate induced?

A

-induced in dorsal ectoderm where BMP is inibited

by BMP antagonists released by organiser

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8
Q

what TFs are released ventrally?

A

BMP4

tolloid

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9
Q

what happens to spemann organiser once it begins to induce the neural plate?

A

It differentiates into axial mesoderm

notochord, prechordal mesoderm, anterior endoderm

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10
Q

what happens to AM when spemann organiser is differentiated?

A

axial mesoderm involutes, intercalates and undergoes convergent extension - extends anteriorly.
-released BMP antagonists

(led by leading edge cells)

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11
Q

what happens in convergent extension?

A

sheet of cells changes shape by extending in one direction and narrowing and converging in another. (cells intercalate)

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12
Q

where are BMP antagonists maintained in axial mesoderm?

A
  • BMP antagonists are only maintained in the prechordal mesoderm.
  • node changes and node and notochord stop producing BMP antagonists (promote proliferation and posteriorisation)
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13
Q

what are the characteristics of the late node and notochord?

A
  • change BMP antagonistic properties

- - have new characteristics which promote proliferation and growth of neural cells and POSTERIORISATION

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14
Q

what are posteriorising signals?

A
  • Fgf, Wnt and RA

- promote growth and posteriorisation

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15
Q

where are BMP and Wnt antagonists maintained?

A

maintained anteriorly in prechordal mesoderm

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16
Q

what do the specialised border of cells at the edge of the neural plate and ectoderm express?

A

msx

17
Q

what leads to dorsalisation?

A

Bmps work with Wnts and FGF signalling toinitiate cascade of events which lead to dorsalisation
-gives rise to NCCs

18
Q

what are edge cells crucial for?

A
  • neural crest cell formation
  • patterning of the dorsal NT
  • roof plate formation
19
Q

how does neural tube ventralisation occur?

A
  • there is secreted Shh in notochord and then floorplate
  • Shh acts as a morphogen to induce different progenitor cells along D-V axis of future spinal cord
  • Shh diffused from NT and FP to induce a conc gradient - cells have different thresholds - different responses to Shh gradient
  • different TFs are induced in bands of of different progenitors along DV axis - read out of Shh gradient
20
Q

where do differentiating cells move?

A

move laterally

21
Q

Give the pathway from the ectoderm when BMP antagonists are present

A
  • ectoderm exposed to BMP antagonists
  • low Smad1, high smad 7
  • neuralating TFs activated
  • neurogenin
  • neuroD
  • neural differentiation
22
Q

Give the pathway from the ectoderm when BMP is present

A

ectoderm - exposed to BMPs

  • hgh smad1, low smad 7
  • epidermalizing TFs
  • LEF1
  • epidermal differentiation