Tcf7L2 is essential for neurogenesis in the developing mouse neocortex
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
P305/12/2042
Grantová Agentura České Republiky - International
18-00514S
Grantová Agentura České Republiky - International
15-25100S
Grantová Agentura České Republiky - International
PubMed
29751817
PubMed Central
PMC5946422
DOI
10.1186/s13064-018-0107-8
PII: 10.1186/s13064-018-0107-8
Knihovny.cz E-zdroje
- Klíčová slova
- Neocortex, Neurogenenesis, Tcf7L1, Tcf7L2, Wnt signalling,
- MeSH
- buněčná diferenciace genetika MeSH
- chlorid-hydrogenuhličitanové antiportéry MeSH
- down regulace genetika MeSH
- embryo savčí MeSH
- hipokampus cytologie embryologie MeSH
- mutace genetika MeSH
- myši transgenní MeSH
- myši MeSH
- neokortex cytologie embryologie MeSH
- nervové kmenové buňky fyziologie MeSH
- neurogeneze fyziologie MeSH
- neuroglie MeSH
- neurony fyziologie MeSH
- počet buněk MeSH
- proliferace buněk genetika MeSH
- protein 2 podobný transkripčnímu faktoru 7 genetika metabolismus MeSH
- proteiny T-boxu metabolismus MeSH
- proteiny Wnt metabolismus MeSH
- retinální gangliové buňky fyziologie MeSH
- signální transdukce genetika MeSH
- transkripční faktory SOXB1 metabolismus MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- chlorid-hydrogenuhličitanové antiportéry MeSH
- Eomes protein, mouse MeSH Prohlížeč
- protein 2 podobný transkripčnímu faktoru 7 MeSH
- proteiny T-boxu MeSH
- proteiny Wnt MeSH
- Sox2 protein, mouse MeSH Prohlížeč
- Tcf7l2 protein, mouse MeSH Prohlížeč
- transkripční faktory SOXB1 MeSH
Generation of neurons in the embryonic neocortex is a balanced process of proliferation and differentiation of neuronal progenitor cells. Canonical Wnt signalling is crucial for expansion of radial glial cells in the ventricular zone and for differentiation of intermediate progenitors in the subventricular zone. We detected abundant expression of two transcrtiption factors mediating canonical Wnt signalling, Tcf7L1 and Tcf7L2, in the ventricular zone of the embryonic neocortex. Conditional knock-out analysis showed that Tcf7L2, but not Tcf7L1, is the principal Wnt mediator important for maintenance of progenitor cell identity in the ventricular zone. In the absence of Tcf7L2, the Wnt activity is reduced, ventricular zone markers Pax6 and Sox2 are downregulated and the neuroepithelial structure is severed due to the loss of apical adherens junctions. This results in decreased proliferation of radial glial cells, the reduced number of intermediate progenitors in the subventricular zone and hypoplastic forebrain. Our data show that canonical Wnt signalling, which is essential for determining the neuroepithelial character of the neocortical ventricular zone, is mediated by Tcf7L2.
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