氧化应激
程序性细胞死亡
百草枯
转染
细胞生物学
胞浆
细胞质
细胞凋亡
蛋白质聚集
化学
分子生物学
生物
生物化学
基因
酶
作者
Yang Lei,Zhifeng Zhang,Ruixue Lei,Shu Wang,Yang Zhuang,An‐Chun Liu,Yan Wu,Juan Chen,Jun‐Chun Tang,Meng‐Xian Pan,Rui Liu,Weijing Liao,Yugong Feng,Qi Wan,Mei Zheng
摘要
DJ-1 (also called PARK7) is a multifunctional redox-sensitive protein that is protective against oxidative stress-induced cell death. TAR DNA-binding protein 43 (TDP-43) is a major protein component of pathological inclusions in amyotrophic lateral sclerosis and frontotemporal dementia. Reducing ab errant aggregation of TDP-43 is a potential approach to prevent cell death. To investigate whether DJ-1 might inhibit TDP-43 aggregation to exert a protective effect in oxidative stress-induced injury, we tested the protein level and subcellular localization of TDP-43 and DJ-1 in SH-SY5Y cells transfected with wild-type DJ-1, DJ-1 mutant (L166P) cDNA, or DJ-1 siRNA. We show that oxidative stress induced by paraquat leads to the formation of cytosolic TDP-43 aggregation in SH-SY5Y cells. DJ-1 overexpression decreases paraquat-induced cytoplasmic accumulation of TDP-43 in SH-SY5Y cells and protects against paraquat-induced cell death. Transfection of DJ-1 L166P mutant or DJ-1 siRNA leads to increased cytosolic aggregation of TDP-43 in paraquat-treated SH-SY5Y cells and promotes cell death. These data suggest that DJ-1 may protect against oxidative stress-induced cell death through the suppression of cytoplasmic TDP-43 aggregation.
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