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Protein Misfolding, Aggregation, and Autophagy After Brain Ischemia

机译:脑缺血后蛋白质错误折叠,聚集和自噬

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摘要

Ischemic brain injury is a common disorder linked to a variety of diseases. Significant progress has been made in our understanding of the underlying mechanisms. Previous studies show that protein misfolding, aggregation, and multiple organelle damage are major pathological events in postischemic neurons. The autophagy pathway is the chief route for bulk degradation of protein aggregates and damaged organelles. The latest studies suggest that impairment of autophagy contributes to abnormal protein aggregation and organelle damages after brain ischemia. This article reviews recent studies of protein misfolding, aggregation, and impairment of autophagy after brain ischemia.
机译:缺血性脑损伤是与多种疾病相关的常见疾病。我们对基本机制的理解已取得重大进展。先前的研究表明,蛋白质错误折叠,聚集和多细胞器损伤是缺血后神经元中的主要病理事件。自噬途径是蛋白质聚集体和受损细胞器大量降解的主要途径。最新研究表明,自噬受损会导致脑缺血后蛋白质异常聚集和细胞器受损。本文回顾了脑缺血后蛋白质错误折叠,聚集和自噬功能受损的最新研究。

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