Kondo T, Murakami K, Honkaniemi J, Sharp F R, Epstein C J, Chan P H
Department of Neurological Surgery, School of Medicine, University of California, San Francisco 94143, USA.
Brain Res. 1996 Oct 21;737(1-2):321-6. doi: 10.1016/0006-8993(96)00949-3.
We examined hsp70 mRNA expression in the brains of transgenic (Tg) mice overexpressing CuZn-superoxide dismutase and in wild-type (Wt) littermates after 3 min of bilateral common carotid artery occlusion. Significant induction of hsp70 mRNA occurred in the hippocampus, the cortex, and other brain regions of the Tg mice 4 h after ischemia compared to the Wt mice. However, there was no histological damage in the brains of Tg and Wt mice as assessed by both Cresyl violet staining and by TUNEL staining for DNA fragmentation. These data suggest that high levels of CuZn-superoxide dismutase activity increase hsp70 mRNA expression and that intense hsp70 mRNA expression does not predict neuronal damage, even in vulnerable hippocampal CA1 neurons.
我们检测了双侧颈总动脉闭塞3分钟后,过表达铜锌超氧化物歧化酶的转基因(Tg)小鼠及野生型(Wt)同窝小鼠大脑中hsp70 mRNA的表达。与野生型小鼠相比,缺血4小时后转基因小鼠的海马体、皮层及其他脑区中hsp70 mRNA出现显著诱导。然而,通过甲酚紫染色和DNA片段化TUNEL染色评估,转基因和野生型小鼠的大脑均未出现组织学损伤。这些数据表明,高水平的铜锌超氧化物歧化酶活性会增加hsp70 mRNA的表达,且即使在易损的海马体CA1神经元中,强烈的hsp70 mRNA表达也不能预测神经元损伤。