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Carboxy-Terminal Modulator Protein (CTMP) is a mitochondrial protein that sensitizes cells to apoptosis
Authors:Arnaud Parcellier  Lionel A Tintignac  Elena Zhuravleva  Peter Cron  Susanne Schenk  Lana Bozulic  Brian A Hemmings
Institution:1. Metabolic Disease Institute, University of Cincinnati, Cincinnati, OH 45437, USA;2. Department of Pharmacology, Metabolic Diseases and Cell Signaling Laboratory, Research Institute for Medical Sciences, College of Medicine, Chungnam National University, Daejeon 301-131, South Korea;3. Department of Pharmacy, Xijing Hospital, Fourth Military Medical University, Shaanxi, 710032, China;4. Department of Neurosurgery, College of Medicine, Chungnam National University, Daejeon 301-747, South Korea;5. Korea Research Institute of Bioscience and Biotechnology, Daejeon 305-333, South Korea;6. Department of Pharmacology, Korea University College of Medicine, Seoul 136-701, South Korea
Abstract: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 CTMP. 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.
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