GSK3: a multifaceted kinase in Wnt signaling

被引:652
|
作者
Wu, Dianqing [1 ,2 ]
Pan, Weijun [3 ]
机构
[1] Yale Univ, Sch Med, Vasc Biol & Therapeut Program, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Pharmacol, New Haven, CT 06510 USA
[3] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Mol Genet Lab, NIH, Bethesda, MD 20892 USA
关键词
GLYCOGEN-SYNTHASE KINASE-3; RECEPTOR-RELATED PROTEIN-5; BETA-CATENIN; NEGATIVE REGULATOR; STABILIZES AXIN; PPPSP MOTIFS; PHOSPHORYLATION; LRP6; MECHANISM; BINDING;
D O I
10.1016/j.tibs.2009.10.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
GSK3 is one of the few signaling mediators that play central roles in a diverse range of signaling pathways, including those activated by Wnts, hedgehog, growth factors, cytokines, and G protein-coupled ligands. Although the inhibition of GSK3-mediated beta-catenin phosphorylation is known to be the key event in Wnt-beta-catenin signaling, the mechanisms that underlie this event remain incompletely understood. The recent demonstration of GSK3 involvement in Wnt receptor phosphorylation illustrates the multifaceted roles that GSK3 plays in Wnt-beta-catenin signaling. In this review, we will summarize these recent results and offer explanations, hypotheses, and models to reconcile some of these observations.
引用
收藏
页码:161 / 168
页数:8
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