Lu D, Jiang D
Tianjin Neurological Institute.
Zhongguo Ying Yong Sheng Li Xue Za Zhi. 1997 Aug;13(3):224-7.
In order to study the molecular mechanism of the selective vulnerability in central nervous system, the expression and distribution of hsp70 and BCL-2 gene were detected by using Northern blot analysis, in situ hybridization and histochemistry method in transient forebrain ischemia and reperfusion rats. It was found that hsp70 gene expression occurred and the synthesis of BCL-2 protein was inhibited in hippocampalCA1 region vulnerable to ischemia, while BCL-2 protein was stained strongly and the signals of hsp70 were not observed in CA3 region resistant to ischemia. The results indicate that the expression of hsp70 gene may be not only as a marker for neuron ischemia, but also play a protective role in the neuronal injury. BCL-2, meanwhile, may have neuro-protective effect on the ischemic neurons.
为研究中枢神经系统选择性易损性的分子机制,采用Northern印迹分析、原位杂交及组织化学方法,检测短暂性前脑缺血再灌注大鼠中hsp70和BCL-2基因的表达及分布。结果发现,在易缺血的海马CA1区出现hsp70基因表达,BCL-2蛋白合成受到抑制;而在抗缺血的CA3区,BCL-2蛋白染色强,未观察到hsp70信号。结果表明,hsp70基因表达不仅可作为神经元缺血的标志物,还可能在神经元损伤中起保护作用。同时,BCL-2可能对缺血神经元具有神经保护作用。