Cholesterol selectively activates canonical Wnt signalling over non-canonical Wnt signalling

被引:103
|
作者
Sheng, Ren [1 ]
Kim, Hyunjoon [2 ]
Lee, Hyeyoon [2 ]
Xin, Yao [1 ]
Chen, Yong [1 ]
Tian, Wen [1 ]
Cui, Yang [1 ]
Choi, Jong-Cheol [3 ]
Doh, Junsang [3 ]
Han, Jin-Kwan [2 ]
Cho, Wonhwa [1 ]
机构
[1] Univ Illinois, Dept Chem, Chicago, IL 60607 USA
[2] Div Mol & Life Sci, Pohang 790784, South Korea
[3] Pohang Univ Sci & Technol, Dept Mech Engn, Pohang 790784, South Korea
来源
NATURE COMMUNICATIONS | 2014年 / 5卷
基金
美国国家卫生研究院; 新加坡国家研究基金会;
关键词
DISHEVELLED DEP DOMAIN; PLASMA-MEMBRANE; PDZ DOMAIN; PROTEIN; BINDING; INHIBITION; LRP6; MECHANISM; REQUIRES; PATHWAY;
D O I
10.1038/ncomms5393
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Wnt proteins control diverse biological processes through beta-catenin-dependent canonical signalling and beta-catenin-independent non-canonical signalling. The mechanisms by which these signalling pathways are differentially triggered and controlled are not fully understood. Dishevelled (Dvl) is a scaffold protein that serves as the branch point of these pathways. Here, we show that cholesterol selectively activates canonical Wnt signalling over non-canonical signalling under physiological conditions by specifically facilitating the membrane recruitment of the PDZ domain of Dvl and its interaction with other proteins. Single-molecule imaging analysis shows that cholesterol is enriched around the Wnt-activated Frizzled and low-density lipoprotein receptor-related protein 5/6 receptors and plays an essential role for Dvl-mediated formation and maintenance of the canonical Wnt signalling complex. Collectively, our results suggest a new regulatory role of cholesterol in Wnt signalling and a potential link between cellular cholesterol levels and the balance between canonical and non-canonical Wnt signalling activities.
引用
收藏
页数:13
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