Wnt5a-mediated non-canonical Wnt signalling regulates human endothelial cell proliferation and migration

被引:120
|
作者
Cheng, Ching-wen
Yeh, Ju-ching
Fan, Tai-Ping
Smith, Stephen K.
Charnock-Jones, D. Stephen
机构
[1] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
[2] Rosie Hosp, Dept Obstet & Gynaecol, Cambridge CB2 2SW, England
[3] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1PD, England
基金
英国医学研究理事会;
关键词
Wnt; non-canonical; endothelial;
D O I
10.1016/j.bbrc.2007.10.166
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
Cell to cell interaction is one of the key processes effecting angiogenesis and endothelial cell function. Wnt signalling is mediated through cell-cell interaction and is involved in many developmental processes and cellular functions. In this study, we investigated the possible function of Wnt5a and the non-canonical Wnt pathway in human endothelial cells. We found that Wnt5a-mediated non-canonical Writ signalling regulated endothelial cell proliferation. Blocking this pathway using antibody, siRNA or a down-stream inhibitor led to suppression of endothelial cell proliferation, migration, and monolayer wound closure. We also found that the mRNA level of Wnt5a is up-regulated when endothelial cells are treated with a cocktail of inflammatory cytokines. Our findings suggest non-canonical Writ signalling plays a role in regulating endothelial cell growth and possibly in angiogenesis. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:285 / 290
页数:6
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