Template:Blastocyst Hippo table: Difference between revisions

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! Mouse blastocyst (32 cell stage)
! Mouse Blastocyst (32 cell stage) Fate
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| width=400px|phosphorylation of angiomotin (Amot) at adherens junctions
| width=400px|phosphorylation of angiomotin (Amot) at adherens junctions
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| trophectoderm (TE) fate<br>
| trophectoderm (TE) fate<br>
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| colspan=2|Table data see review{{#pmid:25986053|PMID25986053}}<br>
| Notch inactive
Notch signaling also has a role in blastocyst fate development.
| Notch active
| colspan=2|[[Developmental Signals - Hippo|Hippo]]{{#pmid:25986053|PMID25986053}}(TEAD4) and [[Developmental Signals - Notch|Notch]]{{#pmid:25127056|PMID25127056}}(Cdx2) together appear regulate early blastocyst fate development.
 
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Revision as of 10:22, 21 March 2018

Mouse Blastocyst (32 cell stage) Fate
phosphorylation of angiomotin (Amot) at adherens junctions cell polarization sequesters Amot from basolateral adherens junctions
active Hippo signaling inactive Hippo signaling
inner cells outer cells
inner cell mass (ICM) fate
trophectoderm (TE) fate
Notch inactive Notch active Hippo[1](TEAD4) and Notch[2](Cdx2) together appear regulate early blastocyst fate development.
  1. Sasaki H. (2015). Position- and polarity-dependent Hippo signaling regulates cell fates in preimplantation mouse embryos. Semin. Cell Dev. Biol. , 47-48, 80-7. PMID: 25986053 DOI.
  2. Rayon T, Menchero S, Nieto A, Xenopoulos P, Crespo M, Cockburn K, Cañon S, Sasaki H, Hadjantonakis AK, de la Pompa JL, Rossant J & Manzanares M. (2014). Notch and hippo converge on Cdx2 to specify the trophectoderm lineage in the mouse blastocyst. Dev. Cell , 30, 410-22. PMID: 25127056 DOI.