细胞死亡与内质网应激:疾病关联性及治疗机遇
Cell death and endoplasmic reticulum stress: disease relevance and therapeutic opportunities.
作者信息
Kim Inki, Xu Wenjie, Reed John C
机构信息
Burnham Institute for Medical Research, 10901 North Torrey Pines Road, La Jolla, California 92037, USA.
出版信息
Nat Rev Drug Discov. 2008 Dec;7(12):1013-30. doi: 10.1038/nrd2755.
The accumulation of unfolded proteins in the endoplasmic reticulum (ER) represents a cellular stress induced by multiple stimuli and pathological conditions. These include hypoxia, oxidative injury, high-fat diet, hypoglycaemia, protein inclusion bodies and viral infection. ER stress triggers an evolutionarily conserved series of signal-transduction events, which constitutes the unfolded protein response. These signalling events aim to ameliorate the accumulation of unfolded proteins in the ER; however, when these events are severe or protracted they can induce cell death. With the increasing recognition of an association between ER stress and human diseases, and with the improved understanding of the diverse underlying molecular mechanisms, novel targets for drug discovery and new strategies for therapeutic intervention are beginning to emerge.
内质网(ER)中未折叠蛋白的积累代表了由多种刺激和病理状况诱导的细胞应激。这些刺激和病理状况包括缺氧、氧化损伤、高脂饮食、低血糖、蛋白质包涵体和病毒感染。内质网应激触发了一系列进化上保守的信号转导事件,这构成了未折叠蛋白反应。这些信号事件旨在改善内质网中未折叠蛋白的积累;然而,当这些事件严重或持续时间过长时,它们会诱导细胞死亡。随着对内质网应激与人类疾病之间关联的认识不断增加,以及对各种潜在分子机制的理解不断深入,药物发现的新靶点和治疗干预的新策略开始出现。