Carboxy-Terminal Modulator Protein (CTMP) is a mitochondrial protein that sensitizes cells to apoptosis

被引:29
|
作者
Parcellier, Arnaud [1 ]
Tintignac, Lionel A. [1 ]
Zhuravleva, Elena [1 ]
Cron, Peter [1 ]
Schenk, Susanne [1 ]
Bozulic, Lana [1 ]
Hemmings, Brian A. [1 ]
机构
[1] Friedrich Miescher Inst Biomed Res, CH-4058 Basel, Switzerland
关键词
CTMP; PKB; Mitochondria; Apoptosis; CYTOCHROME-C RELEASE; WOLF-HIRSCHHORN-SYNDROME; AKT/PROTEIN KINASE-B; IN-VIVO; DNA-PK; PHOSPHATIDYLINOSITOL; 3-KINASE; AKT PHOSPHORYLATION; MICE REVEALS; NULL MICE; ACTIVATION;
D O I
10.1016/j.cellsig.2009.01.016
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Carboxy-Terminal Modulator Protein (CTMP) protein was identified as a PKB inhibitor that binds to its hydrophobic motif Here, we report mitochondrial localization of endogenous and exogenous CTMR CTMP exhibits a dual sub-mitochondrial localization as a membrane-bound pool and a free pool of mature CTMP in the inter-membrane space. CTMP is released from the mitochondria into the cytosol early upon apoptosis. CTMP overexpression is associated with an increase in mitochondrial membrane depolarization and caspase-3 and polyADP-ribose polymerase (PARP) cleavage. In contrast, CTMP knock-down results in a marked reduction in the loss of mitochondrial membrane potential as well as a decrease in caspase-3 and PARP activation. Mutant CTMP retained in the mitochondria loses its capacity to sensitize cells to apoptosis. Thus, proper maturation of CTMP is essential for its pro-apoptotic function. Finally, we demonstrate that CTMP delays PKB phosphorylation following cell death induction, suggesting that CTMP regulates apoptosis via inhibition of PKB. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:639 / 650
页数:12
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