Human nuclear clusterin mediates apoptosis by interacting with Bcl-XL through C-terminal coiled coil domain

被引:49
|
作者
Kim, Nayoung [1 ]
Yoo, Jae Cheal
Han, Jae Yoon [1 ]
Hwang, Eun Mi
Kim, Yoon Sook [1 ]
Jeong, Eun Young [1 ]
Sun, Choong-Hyun [3 ]
Yi, Gwan-Su [3 ]
Roh, Gu Seob [1 ]
Kim, Hyun Joon [1 ]
Kang, Sang Soo [1 ]
Cho, Gyeong Jae [1 ]
Park, Jae-Yong [2 ]
Choi, Wan Sung [1 ]
机构
[1] Gyeongsang Natl Univ, Sch Med, Med Res Ctr Neural Dysfunct, Dept Anat & Neurobiol, Jinju 660751, Gyeongnam, South Korea
[2] Gyeongsang Natl Univ, Sch Med, Dept Physiol, Inst Hlth Sci, Jinju 660751, Gyeongnam, South Korea
[3] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
基金
新加坡国家研究基金会;
关键词
clusterin; apoptosis; Bcl-XL; PROSTATE-CANCER CELLS; MITOCHONDRIAL APOPTOSIS; BH3-ONLY PROTEINS; PEPTIDE COMPLEX; BH3; DOMAINS; FAMILY-MEMBERS; TNF-ALPHA; BAX; DEATH; MCL-1;
D O I
10.1002/jcp.22836
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Clusterin (CLU), a glycoprotein, is involved in apoptosis, producing two alternatively spliced isoforms in various cell types. The pro-apoptotic CLU appears to be a nuclear isoform (nuclear clusterin; nCLU), and the secretory CLU (sCLU) is thought to be anti-apoptotic. The detailed molecular mechanism of nCLU as a pro-apoptotic molecule has not yet been clear. In the current study, overexpressed nCLU induced apoptosis in human kidney cells. Biochemical studies revealed that nCLU sequestered Bcl-XL via a putative BH3 motif in the C-terminal coiled coil (CC2) domain, releasing Bax, and promoted apoptosis accompanied by activation of caspase-3 and cytochrome c release. These results suggest a novel mechanism of apoptosis mediated by nCLU as a pro-apoptotic molecule. J. Cell. Physiol. 227: 11571167, 2012. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:1157 / 1167
页数:11
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