Developmental Processes Flashcards

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1
Q

what is polarisation

A

form apical complex

driving force behind the first lineage restriction

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2
Q

what cells become polarised

A

TE cells become polarised, while ICM cells lack apical/basal polarity

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3
Q

what is asymmetric cell div

A

segregation of apical complex

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4
Q

what sit he cell position

A

suppression of apical complex in inner cells

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5
Q

what is cell fate

A

restricted expression of lineage sp genes

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6
Q

what are the signalling centres

A

organiser
dorsal blastopore lip on ventral side of unpigmented host embryo
new neural tube
second embryo form

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7
Q

what are signalling gradients

A

positional info

cells respond in sp way dept on conc of signal mol

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8
Q

what do signalling gradients regulate

A

differentiation in the neural tube by providing positional info

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9
Q

where is Shh prod

A

in notochord and floor plate

diffuses dorsally

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10
Q

where is high levels Shh found

A

cells near floor plate

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11
Q

when does Shh conc decrease

A

dorsally giving rise to diff cell types

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12
Q

what happens if more Shh is added dorsally

A

change in cell fate due to and increase conc Shh

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13
Q

what are dorsal cell after induced by

A

TGF(beta) signalling

opposes effects of Shh

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14
Q

what does programmed cll death do

A

help shape embryo

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15
Q

what does BMP4 signalling trigger

A

cell death programme in interdigital zones of foot and hand

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16
Q

what do localised changes in shape in neuralation lead to

A

folding of neural plate at median an dorso-lateral hinge points

17
Q

where does tissue fusion occur

A

as edges of neural plate together

18
Q

what is imp for formation of face

A

tissue folding

19
Q

how many facial swellings

A

5

20
Q

when is there cell migration

A

gastrulation
neural crest
germ cells
interneurons

21
Q

what is epithelial cell state

A

cells in sheets with specialised mem contacts adherent and tight junctions

22
Q

what is mesenchymal cell state

A

loosely assc often motile cells with only transient focal attachments to other cells

23
Q

transition between epi cell state and mesenchymal cells state required for

A
gastrulation 
neural crest 
vertebrae
cardiac valves
secondary palate formation
24
Q

essentially what is `EMT

A

tissue remodelling

25
Q

what si the EMT pathwa

A

extra cell signals - signal mol and GF’s

transcription factors which repress key cell adhesion molecules

E- Cadherin caretaker of epi cell state

26
Q

what are 90% oral cancers have EMT

A

squamous cell carcinomas often characterised by low E-Cadherin expression