Wnt-3a regulates chondrocyte differentiation via c-Jun/AP-1 pathway

被引:94
作者
Hwang, SG
Yu, SS
Lee, SW
Chun, JS [1 ]
机构
[1] Gwangju Inst Sci & Technol, Dept Life Sci, Kwangju 500712, South Korea
[2] Inje Univ, Coll Med, Ctr Viral Dis Res, Pusan 614735, South Korea
来源
FEBS LETTERS | 2005年 / 579卷 / 21期
关键词
Wnt-3a; beta-catenin; chondrogenesis; chondrocyte; dedifferentiation;
D O I
10.1016/j.febslet.2005.07.067
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
Our previous study indicated that interleukin (IL)-1 beta induces expression of several Wnt proteins in chondrocytes and causes chondrocyte dedifferentiation via the c-Jun/activator protein-1 (AP-1) pathway. This study examined whether Wnt-3a causes chondrocyte dedifferentiation via the e-Jun/AP-1 pathway. Wnt-3a inhibited chondrogenesis of mesenchymal cells by stabilizing cell-cell adhesion in a manner independent of P-catenin transcriptional activity. Wnt-3a also induced dedifferentiation of articular chondrocytes by stimulating the transcriptional activity of beta-catenin-T cell-factor/lymphoid-enhancer-factor (Tcf/Lef) complex. In chondrocytes, Wnt-3a caused the expression of c-Jun and its phosphorylation by c-Jun N-terminal kinase (JNK), resulting in activation of AP-1. AP-I activation suppressed the expression of Sox-9, a major transcription factor regulating type 11 collagen expression. Collectively, our results suggest that Wnt-3a inhibits chondrogenesis by stabilizing cell-cell adhesion and that it causes dedifferentiation of chondrocytes by activating of beta-catenin-Tcf/Lef transcriptional complex and the c-Jun/AP-1 pathway. (c) 2005 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:4837 / 4842
页数:6
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