Journal
JOURNAL OF CELLULAR BIOCHEMISTRY
Volume 111, Issue 1, Pages 94-103Publisher
WILEY-BLACKWELL
DOI: 10.1002/jcb.22666
Keywords
MsrA; ANOXIA/REOXYGENATION; CELL DEATH; siRNA
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Funding
- NIH [HL-58435, HL-061246]
- American Heart Association
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Methionne sulfoxide reductase A (MsrA), a member of the Msr gene family. can reduce methionne sulfoxide residues in proteins formed by oxidation or methionne by reactive oxygen species (ROS). Msr is an Important protein repair system which can also function to scavenge ROS. Our studies have confirmed the expression of MsrA in mouse embryonic stem cells (ESCs) in culture conditions. A cytosol-located and mitochondria-ennched expression pattern has been observed in these cells. To confirm the protective function of MsrA in ESCs against oxidative stress, a siRNA approach has been used to knockdown MsrA expression in ES cells which showed less resistance than control cells to hydrogen peroxide treatment. Overexpression of MsrA gene products in ES cells showed improved survivability of these cells to hydrogen peroxide treatment. Our results indicate that MsrA plays an important role in cellular defenses against oxidative stress in ESCs. Msr genes may provide a new target in stem cells to increase their survivability during the therapeutic applications J. Cell. Biochem 111. 94-103, 2010 (C)2010 Wiley-Liss, Inc
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