Cystine glutamate exchanger upregulation by retinoic acid induces neuroprotection in neural stem cells

被引:16
作者
Crockett, Stephanie [4 ]
Clarke, Melinda
Reeves, Shari
Sims, Brian [1 ,2 ,3 ]
机构
[1] Univ Alabama Birmingham, Dept Pediat, Div Neonatol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Cell Biol, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Ctr Glial Biol Med, Birmingham, AL 35294 USA
[4] Univ Calif Davis, Dept Comparat Pathol, Birmingham, AL USA
关键词
glutathione biosynthesis; neural stem cells; retinoic acid; system Xc(-); OXIDATIVE STRESS; EXPRESSION; APOPTOSIS; X(C)(-); NEURONS; TARGET;
D O I
10.1097/WNR.0b013e3283494359
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Oxidative stress and excitotoxic injury are commonly associated with several neurodegenerative diseases, such as Parkinson's disease, Alzheimer's disease, and periventricular leukomalacia. As cystine is imported into the cell, it is used in the synthesis of intracellular glutathione, an important antioxidant necessary for the defense of brain cells from oxidative stress and glutamate-mediated excitotoxicity. Recent studies have shown that retinoic acid increases the activity of glutathione synthesis and exhibits neuroprotective properties in brain cells. Previously, we have shown that the regulation of the cystine glutamate exchanger (system Xc(-)) also leads to neuroprotection. Here, we examined the effects of retinoic acid on the regulation of system Xc(-). Our results suggest that retinoic acid-induced neuroprotection is mediated through system Xc(-) by regulating glutathione biosynthesis. NeuroReport 22:598-602 (C) 2011 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:598 / 602
页数:5
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