| Literature DB >> 19265663 |
Sebastian Fuchs1, Dominik Herzog, Grzegorz Sumara, Stine Büchmann-Møller, Gianluca Civenni, Xunwei Wu, Anna Chrostek-Grashoff, Ueli Suter, Romeo Ricci, João B Relvas, Cord Brakebusch, Lukas Sommer.
Abstract
The neural crest (NC) generates a variety of neural and non-neural tissues during vertebrate development. Both migratory NC cells and their target structures contain cells with stem cell features. Here we show that these populations of neural crest-derived stem cells (NCSCs) are differentially regulated by small Rho GTPases. Deletion of either Cdc42 or Rac1 in the NC results in size reduction of multiple NC target structures because of increased cell-cycle exit, while NC cells emigrating from the neural tube are not affected. Consistently, Cdc42 or Rac1 inactivation reduces self-renewal and proliferation of later stage, but not early migratory NCSCs. This stage-specific requirement for small Rho GTPases is due to changes in NCSCs that, during development, acquire responsiveness to mitogenic EGF acting upstream of both Cdc42 and Rac1. Thus, our data reveal distinct mechanisms for growth control of NCSCs from different developmental stages.Entities:
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Year: 2009 PMID: 19265663 DOI: 10.1016/j.stem.2009.01.017
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633