Human brain thioltransferase: constitutive expression and localization by fluorescence in situ hybridization

被引:12
作者
Balijepalli, S
Boyd, MR
Ravindranath, V
机构
[1] Natl Inst Mental Hlth & Neurosci, Dept Neurochem, Bangalore 560029, Karnataka, India
[2] Natl Brain Res Ctr, New Delhi 110067, India
[3] NCI, Frederick Canc Res & Dev Ctr, Lab Drug Discovery Res & Dev, Dev Therapeut Program, Frederick, MD 21702 USA
来源
MOLECULAR BRAIN RESEARCH | 2000年 / 85卷 / 1-2期
关键词
thiol disulfide oxidoreductase; thioltransferase; oxidative stress; brain; glutathione; human;
D O I
10.1016/S0169-328X(00)00206-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Thioltransferase (glutaredoxin) is a member of the family of thiol-disulfide oxido-reductases that maintain the sulfhydryl homeostasis in cells by catalyzing thiol-disulfide interchange reactions. One of the major consequences of oxidative stress in brain is formation of protein-glutathione mixed disulfide (through oxidation of protein thiols) which can be reversed by thioltransferase during recovery of brain from oxidative stress. Here we have visualized the location of thioltransferase in brain regions from seven human tissues obtained at autopsy. Constitutively expressed thioltransferase activity was detectable in all human brains examined although inter-individual variations were seen. The enzyme activity was significantly higher in hippocampus and cerebellum as compared to other regions. Constitutive expression of thioltransferase mRNA was detectable by Northern blot analysis. Localization of thioltransferase mRNA by fluorescence in situ hybridization revealed its presence predominantly in neurons in the cerebral cortex, Purkinje and granule cell layers of the cerebellum granule cell layer of the dentate gyrus and in the pyramidal neurons of CAI, CA2 and CA3 subfields of hippocampus. These discrete neuronal concentrations of thioltransferase would be consistent with an essential role in modulating recovery of protein thiols from mixed disulfides formed during oxidative stress. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:123 / 132
页数:10
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