Beneficial effect of taurine on hypoxia- and glutamate-induced endoplasmic reticulum stress pathways in primary neuronal culture

被引:68
作者
Pan, Chunliu [2 ]
Prentice, Howard [1 ]
Price, Allison L. [3 ]
Wu, Jang-Yen [1 ]
机构
[1] Florida Atlantic Univ, Dept Biomed Sci, Boca Raton, FL 33431 USA
[2] Florida Atlantic Univ, Dept Chem & Biochem, Boca Raton, FL 33431 USA
[3] Florida Atlantic Univ, Univ Miami, Miller Sch Med, Boca Raton, FL 33431 USA
关键词
Taurine; Neuroprotection; Hypoxia; Endoplasmic reticulum stress; Glutamate; INITIATION-FACTOR; 2-ALPHA; CEREBRAL-ISCHEMIA; INDUCED APOPTOSIS; ER STRESS; ACTIVATION; EXPRESSION; PROTECTION; EXCITOTOXICITY; NEUROTOXICITY; CASPASE-12;
D O I
10.1007/s00726-011-1141-6
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
Stroke (hypoxia) is one of the leading causes of mortality in the developed countries, and it can induce excessive glutamate release and endoplasmic reticulum (ER) stress. Taurine, as a free amino acid, present in high concentrations in a range of organs in mammals, can provide protection against multiple neurological diseases. Here, we present a study to investigate the potential protective benefits of taurine against ER stress induced by glutamate and hypoxia/reoxygenation in primary cortical neuronal cultures. We found that taurine suppresses the up-regulation of caspase-12 and GADD153/CHOP induced by hypoxia/reoxygenation, suggesting that taurine may exert a protective function against hypoxia/reoxygenation by reducing the ER stress. Moreover, taurine can down-regulate the ratio of cleaved ATF6 and full length ATF6, and p-IRE1 expression, indicating that taurine inhibits the ER stress induced by hypoxia/reoxygenation and glutamate through suppressing ATF6 and IRE1 pathways.
引用
收藏
页码:845 / 855
页数:11
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