Human Nogo-C overexpression induces HEK293 cell apoptosis via a mechanism that involves JNK-c-Jun pathway

被引:33
作者
Chen, Yicun [1 ]
Tang, Xiaojun [1 ]
Cao, Xiangrong [1 ]
Chen, Huaqun [1 ]
Zhang, Xiran [1 ]
机构
[1] Nanjing Normal, Jiangsu Key Lab Mol & Med Biotechnol, Coll Life Sci, Nanjing 210097, Peoples R China
关键词
Nogo-C; apoptosis; JNK/SAPK; c-Jun;
D O I
10.1016/j.bbrc.2006.07.166
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
The neurite outgrowth inhibitor protein Nogo-A has been identified as an inhibitor of axonal regeneration, and Nogo-B as a regulator of vasculature remodeling, but the additional roles of Nogo isoforms, especially Nogo-C, have obtained little attention. Nogo-C is weakly expressed in liver and kidney compared to the high expression in skeletal muscle. Here we detected the weak expression of Nogo-C in human embryonic kidney cell line HEK293, and found that Nogo-C expressed in HEK293 could induce cell apoptosis. Further experiments demonstrated the activation of JNK/SAPK and c-Jun, but not p38 in Nogo-C expressed cells. And JNK-specific inhibitor SP600125 could reduce cell apoptosis induced by Nogo-C. Furthermore, the activation of caspase-3 and PARP, the expression and phosphorylation of p53 were also detected. The data first revealed Nogo-C expressed in HEK293 confers apoptosis by inducing caspase-3 and p53 activation through the JNK-c-Jun-dependent pathway. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:923 / 928
页数:6
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