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姜酚通过 PINK1 诱导的线粒体结构蛋白 Mic60 减少 SH-SY5Y 细胞细胞色素 c 的释放。

Carnosic acid attenuated cytochrome c release through the mitochondrial structural protein Mic60 by PINK1 in SH-SY5Y cells.

机构信息

Department of Nutrition, China Medical University, Taichung, Taiwan.

Department of Chinese Pharmaceutical Sciences and Chinese Medicine Resources, China Medical University, Taichung, Taiwan.

出版信息

Food Chem Toxicol. 2023 Mar;173:113636. doi: 10.1016/j.fct.2023.113636. Epub 2023 Jan 25.

Abstract

Mitochondrial dysfunction has been implicated in Parkinson's disease. Mic60 is a critical component of mitochondrial crista remodeling and participates in maintaining mitochondrial structure and function. This study investigated whether the carnosic acid (CA) of rosemary protects the mitochondria of SH-SY5Y cells against the neurotoxicity of 6-hydroxydopamine (6-OHDA) by regulating Mic60. Our results showed that CA pretreatment reversed the reduction in the Mic60 and citrate synthase proteins, as well as the protein induction of PKA caused by 6-OHDA. Moreover, Mic60 and PINK1 siRNAs blocked the ability of CA to lessen the release of mitochondrial cytochrome c by 6-OHDA. As shown by immunoprecipitation assay, in 6-OHDA-treated cells, the interaction of Mic60 with its phosphorylated threonine residue was decreased, but the interaction with its phosphorylated serine residue was increased. PINK1 siRNA and forskolin, a PKA activator, reversed these interactions. Moreover, forskolin pretreatment prevented CA from rescuing the interaction of PINK1 and Mic60 and the reduction in cytochrome c release and mitophagy impairment in 6-OHDA-treated cells. In conclusion, CA prevents 6-OHDA-induced cytochrome c release by regulating Mic60 phosphorylation by PINK1 through a downregulation of PKA. The regulation of Mic60 by CA can be considered as a protective mechanism for the prevention of Parkinson's disease.

摘要

线粒体功能障碍与帕金森病有关。Mic60 是线粒体嵴重塑的关键组成部分,参与维持线粒体结构和功能。本研究探讨了迷迭香酸(CA)是否通过调节 Mic60 来保护 SH-SY5Y 细胞的线粒体免受 6-羟多巴胺(6-OHDA)的神经毒性。我们的结果表明,CA 预处理逆转了 6-OHDA 引起的 Mic60 和柠檬酸合酶蛋白减少以及 PKA 蛋白诱导。此外,Mic60 和 PINK1 siRNA 阻断了 CA 减轻 6-OHDA 引起的线粒体细胞色素 c 释放的能力。免疫沉淀试验显示,在 6-OHDA 处理的细胞中,Mic60 与其磷酸化苏氨酸残基的相互作用减少,但与磷酸化丝氨酸残基的相互作用增加。PINK1 siRNA 和 PKA 激活剂 forskolin 逆转了这些相互作用。此外,福司可林预处理可防止 CA 挽救 PINK1 和 Mic60 的相互作用,以及减轻 6-OHDA 处理细胞中细胞色素 c 释放减少和线粒体自噬受损。总之,CA 通过下调 PKA 调节 PINK1 对 Mic60 的磷酸化来防止 6-OHDA 诱导的细胞色素 c 释放。CA 对 Mic60 的调节可被视为预防帕金森病的保护机制。

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