Overexpression of mitochondrial Hsp70/Hsp75 protects astrocytes against ischemic injury in vitro

被引:100
|
作者
Voloboueva, Ludmila A. [1 ]
Duan, Melissa [1 ]
Ouyang, YiBing [1 ]
Emery, John F. [1 ]
Stoy, Christian [1 ]
Giffard, Rona G. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
来源
关键词
astrocyte; mitochondria; ischemia; oxidative stress; heat shock protein; mortalin;
D O I
10.1038/sj.jcbfm.9600600
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mitochondrial heat shock protein 70 (mtHsp70/Hsp75/Grp75/mortalin/TRAP-1/PBP74) is an essential mitochondrial chaperone and a member of the heat shock protein 70 (HSP70) family. Although many studies have shown the protective properties of overexpression of the cytosolic inducible member of the HSP70 family, Hsp72, few studies have investigated the protective potential of Hsp75 against ischemic injury. Mitochondria are one of the primary targets of ischemic injury in astrocytes. In this study, we analyzed the effects of Hsp75 overexpression on cellular levels of reactive oxygen species (ROS), mitochondrial membrane potential, ATP levels, and viability during the ischemia-like conditions of oxygen-glucose deprivation (OGD) or glucose deprivation (GD) in primary astrocytic cultures. We show that Hsp75 overexpression decreases ROS production and preserves mitochondrial membrane potential during GD, and preserves ATP levels and cell viability during OGD. These findings indicate that Hsp75 can provide protection against ischemia-like in vitro injury and suggest that it should be further studied as a potential candidate for protection against ischemic injury.
引用
收藏
页码:1009 / 1016
页数:8
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