Calcium transport across the inner mitochondrial membrane: Molecular mechanisms and pharmacology

被引:44
作者
Csordas, Gyoergy [1 ]
Varnai, Peter [2 ]
Golenar, Tuende [1 ]
Shen, Shey-Shing [3 ]
Hajnoczky, Gyoergy [1 ]
机构
[1] Thomas Jefferson Univ, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
[2] Semmelweis Univ Budapest, Dept Physiol, Budapest, Hungary
[3] Thomas Jefferson Univ, Ctr Translat Med, Philadelphia, PA 19107 USA
基金
英国医学研究理事会; 匈牙利科学研究基金会;
关键词
Mitochondria; Uniporter; Ruthenium red; Ru360; CGP-37157; Minocycline; SARCOPLASMIC-RETICULUM; ENDOPLASMIC-RETICULUM; SIGNAL TRANSMISSION; CA2+; MINOCYCLINE; UNIPORTER; CHANNELS; HOMEOSTASIS; ACTIVATION; EXCHANGE;
D O I
10.1016/j.mce.2011.11.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Growing evidence supports that mitochondrial calcium uptake is important for cell metabolism, signaling and survival. However, both the molecular nature of the mitochondrial Ca2+ transport sites and the calcium signals they respond to remained elusive. Recent RNA interference studies have identified new candidate proteins for Ca2+ transport across the inner mitochondrial membrane, including LETM1, MCU, MICU1 and NCLX. The sensitivity of these factors to several drugs has been tested and in parallel, some new inhibitors of mitochondrial Ca2+ uptake have been described. This paper provides an update on the pharmacological aspects of the molecular mechanisms of the inner mitochondrial membrane Ca2+ transport. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:109 / 113
页数:5
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