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线粒体功能在细胞死亡和机体代谢中的作用。

Role of mitochondrial function in cell death and body metabolism.

机构信息

Severance Biomedical Science Institute and Department of Internal Medicine, Yonsei University College of Medicine, Yonsei-ro 50-1,Seodaemun-gu, Seoul 03722, Korea,

出版信息

Front Biosci (Landmark Ed). 2016 Jun 1;21(6):1233-44. doi: 10.2741/4453.

Abstract

Mitochondria are the key players in apoptosis and necrosis. Mitochondrial DNA (mtDNA)-depleted r0 cells were resistant to diverse apoptosis inducers such as TNF-alpha, TNFSF10, staurosporine and p53. Apoptosis resistance was accompanied by the absence of mitochondrial potential loss or cytochrome c translocation. r0 cells were also resistant to necrosis induced by reactive oxygen species (ROS) donors due to upregulation of antioxidant enzymes such as manganese superoxide dismutase. Mitochondria also has a close relationship with autophagy that plays a critical role in the turnover of senescent organelles or dysfunctional proteins and may be included in 'cell death' category. It was demonstrated that autophagy deficiency in insulin target tissues such as skeletal muscle induces mitochondrial stress response, which leads to the induction of FGF21 as a 'mitokine' and affects the whole body metabolism. These results show that mitochondria are not simply the power plants of cells generating ATP, but are closely related to several types of cell death and autophagy. Mitochondria affect various pathophysiological events related to diverse disorders such as cancer, metabolic disorders and aging.

摘要

线粒体是细胞凋亡和坏死的关键参与者。线粒体 DNA(mtDNA)耗竭的 r0 细胞对各种凋亡诱导剂如 TNF-α、TNFSF10、星形孢菌素和 p53 具有抗性。凋亡抗性伴随着线粒体膜电位丧失或细胞色素 c 易位的缺失。r0 细胞还对由于抗氧化酶如锰超氧化物歧化酶的上调而引起的活性氧(ROS)供体诱导的坏死具有抗性。线粒体还与自噬密切相关,自噬在衰老细胞器或功能失调蛋白质的周转中起着关键作用,可能被包括在“细胞死亡”类别中。已经证明,胰岛素靶组织如骨骼肌中的自噬缺陷会诱导线粒体应激反应,从而导致成纤维细胞生长因子 21(FGF21)作为“线粒体因子”的诱导,并影响全身代谢。这些结果表明,线粒体不仅仅是产生 ATP 的细胞的发电厂,还与多种类型的细胞死亡和自噬密切相关。线粒体影响与癌症、代谢紊乱和衰老等多种疾病相关的各种病理生理事件。

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