The plasma membrane Na+/Ca2+ exchanger is cleaved by distinct protease families in neuronal cell death

被引:25
作者
Bano, D. [1 ]
Munarriz, E. [1 ]
Chen, H. L. [1 ]
Ziviani, E. [1 ]
Lippi, G. [1 ]
Young, K. W. [1 ]
Nicotera, P. [1 ]
机构
[1] Univ Leicester, MRC Toxicol Unit, Leicester LE1 9HN, Leics, England
来源
SODIUM-CALCIUM EXCHANGE AND THE PLASMA MEMBRANE CA2+-ATPASE IN CELL FUNCTION: FIFTH INTERNATIONAL CONFERENCE | 2007年 / 1099卷
关键词
brain ischemia; excitotoxicity; NCX; calcium; calpains; caspase; cell death;
D O I
10.1196/annals.1387.006
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
Neurodegenerative conditions commonly involve loss of neuronal connectivity, synaptic dysfunction with excessive pruning, and ionic imbalances. These often serve as a prelude to cell death either through the activation of apoptotic or necrotic death routines or excess autophagy. In many instances, a local or generalized Ca2+ deregulation is involved in signaling or executing cell death. We have recently shown that in brain ischemia, and during excitotoxicity triggered by excess glutamate, the irreversible Ca2+ deregulation leading to necrosis is due to calpain-mediated modulation of the plasma membrane Na+/Ca2+ exchanger (NCX). Here we show that the NCX can also be cleaved by caspases in neurons undergoing apoptosis, which suggests that cleavage of the main Ca2+ extrusion pathway is a lethal event in multiple forms of cell death.
引用
收藏
页码:451 / 455
页数:5
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