Stage-Specific Control of Neural Crest Stem Cell Proliferation by the Small Rho GTPases Cdc42 and Rac1

被引:78
|
作者
Fuchs, Sebastian [1 ,2 ]
Herzog, Dominik [2 ]
Sumara, Grzegorz [2 ]
Buechmann-Moller, Stine [1 ,2 ]
Civenni, Gianluca [1 ,2 ]
Wu, Xunwei [3 ]
Chrostek-Grashoff, Anna [4 ]
Suter, Ueli [2 ]
Ricci, Romeo [2 ]
Relvas, Joao B. [2 ]
Brakebusch, Cord [5 ]
Sommer, Lukas [1 ,2 ]
机构
[1] Univ Zurich, Inst Anat, CH-8057 Zurich, Switzerland
[2] ETH, Inst Cell Biol, Dept Biol, CH-8093 Zurich, Switzerland
[3] Harvard Univ, Sch Med, MGH, CBRC, Charlestown, MA 02129 USA
[4] Univ Virginia Hlth Syst, Cardiovasc Res Ctr, Charlottesville, VA 22908 USA
[5] Univ Copenhagen, Inst Mol Pathol, DK-2100 Copenhagen, Denmark
基金
瑞士国家科学基金会;
关键词
PERIPHERAL NERVOUS-SYSTEM; SELF-RENEWAL; DIGEORGE-SYNDROME; FAMILY GTPASES; GROWTH-FACTOR; BETA-CATENIN; MIGRATION; MAINTENANCE; PROGENITORS; FATE;
D O I
10.1016/j.stem.2009.01.017
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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.
引用
收藏
页码:236 / 247
页数:12
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