Ouyang Yi-Bing, Xu Lijun, Giffard Rona G
Department of Anesthesia, Grant Building S272, Stanford University School of Medicine, Stanford, CA 94305 5117, USA.
Neurosci Lett. 2005 Jun 3;380(3):229-33. doi: 10.1016/j.neulet.2005.01.055. Epub 2005 Feb 8.
Our prior work demonstrated that geldanamycin (GA) reduced injury due to oxygen-glucose deprivation (OGD) in primary astrocyte cultures. Using medium with an ionic composition similar to that observed during in vivo global ischemia, the selectivity and temporal profile of CA1 neuronal damage seen in vivo was mimicked with OGD in mouse hippocampal organotypic slice cultures. The present study tested the ability of GA to reduce delayed neuronal death in such cultures. Treating organotypic cultures with 100 nM GA for 24 h prior to OGD induced Hsp70 and significantly reduced CA1 neuronal damage. Staining with ubiquitin to identify protein aggregates revealed reduced redistribution of ubiquitin, consistent with reduced protein aggregation likely due at least in part to induction of Hsp70 by GA.
我们之前的研究表明,格尔德霉素(GA)可减轻原代星形胶质细胞培养物中氧糖剥夺(OGD)所致的损伤。使用离子组成与体内全脑缺血时相似的培养基,在小鼠海马器官型脑片培养物中,OGD模拟了体内所见的CA1神经元损伤的选择性和时间特征。本研究测试了GA在此类培养物中减少延迟性神经元死亡的能力。在OGD之前用100 nM GA处理器官型培养物24小时可诱导Hsp70表达,并显著减轻CA1神经元损伤。用泛素染色以识别蛋白质聚集体,结果显示泛素的重新分布减少,这与蛋白质聚集减少一致,这可能至少部分归因于GA诱导的Hsp70。