TGFβ superfamily signaling in the neural crest lineage

被引:16
|
作者
Conway, Simon J.
Kaartinen, Vesa
机构
[1] Univ Michigan, Sch Dent, Ann Arbor, MI 48109 USA
[2] Indiana Univ Sch Med, HB Wells Ctr Pediat Res, Indianapolis, IN USA
基金
美国国家卫生研究院;
关键词
TGF beta; neural crest; heart; cranial crest; mouse transgenics; CARDIAC OUTFLOW TRACT; CELLS LEADS; EXPRESSION; DEFECTS; SMAD4; INACTIVATION; ACTIVATION; MIGRATION; PATHWAYS; ALK5;
D O I
10.4161/cam.5.3.15498
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The neural crest cell (NCC) lineage is often referred to as the fourth germ layer in embryos, as its wide range of migration and early colonization of multiple tissues and organ systems throughout the developing body is astounding. Many human birth defects are thought to have their origins within the NCC lineage. Exciting recent conditional mouse targeting and transgenic combinatorial suppression approaches have revealed that the TGF beta superfamily is a key signaling pathway within the cardiac and cranial NCC subpopulations. Given the complexity of TGF beta superfamily signaling and that multiple ligand and receptor combinations have already been shown to be expressed within the NCC subpopulations, and the difficulty in transgenically targeting entire signaling cascades, we review several up-to-date transgenic approaches that are revealing unexpected consequences.
引用
收藏
页码:232 / 236
页数:5
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