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自噬在线粒体质量控制中的作用。

Autophagy in Mitochondrial Quality Control.

机构信息

Laboratory of Molecular Neuropathology, Jiangsu Key Laboratory of Neuropsychiatric Diseases & Department of Pharmacology, College of Pharmaceutical Sciences, Soochow University, Suzhou, 215123, Jiangsu, China.

出版信息

Adv Exp Med Biol. 2019;1206:421-434. doi: 10.1007/978-981-15-0602-4_19.

Abstract

Autophagy plays an important role in the renewal of cellular components, which function in energy production, metabolism, and clearance of damaged organelles. Both macroautophagy and microautophagy are involved in these processes. Although it was thought that nonselective macroautophagy is responsible for the clearance of damaged or old organelles, recent studies show that the clearance of cellular organelles depends on selective processes. Mitophagy is a process for selective degradation of mitochondria, which is well documented. The selective autophagy for other organelles includes endoplasmic reticulum autophagy (reticulophagy) and peroxisome autophagy (pexophagy). Autophagy is a routine pathway for cells to degrade unused proteins and damaged organelles in cells. Autophagy selectively removes dysfunctional cellular components but not damages the normally functioning organelles, to maintain the homeostasis of cells. In addition to the maintenance of the homeostasis of cells, autophagy clears the damaged organelles in disease or injury conditions to achieve cellular quality control. In some differentiated cells, such as red blood cells, some organelles are removed during the maturation, including mitochondria. The autophagy system can selectively clear the mitochondria and other organelles, which lead to the maturation of red blood cells. Dysfunction of autophagy impairs the clearance of damaged organelles, which results in injury of cells. In the maturation of red blood cells, failure to clear the cellular organelles by autophagy will disturb the normal differentiation of red blood cells, leading to a series of diseases such as anemia.

摘要

自噬在细胞成分的更新中起着重要作用,这些成分在能量产生、代谢和受损细胞器清除中发挥作用。巨自噬和微自噬都参与了这些过程。虽然人们认为非选择性的巨自噬负责清除受损或衰老的细胞器,但最近的研究表明,细胞细胞器的清除依赖于选择性过程。线粒体的选择性降解过程即为自噬,这一点已有充分的文献记载。其他细胞器的选择性自噬包括内质网自噬(网质自噬)和过氧化物酶体自噬(过氧体自噬)。自噬是细胞降解细胞内未使用的蛋白质和受损细胞器的常规途径。自噬选择性地去除功能失调的细胞成分,但不会损伤正常功能的细胞器,以维持细胞的内稳态。除了维持细胞的内稳态外,自噬还可以清除疾病或损伤条件下受损的细胞器,以实现细胞的质量控制。在一些分化细胞中,如红细胞,在成熟过程中会去除一些细胞器,包括线粒体。自噬系统可以选择性地清除线粒体和其他细胞器,从而促进红细胞的成熟。自噬功能障碍会损害受损细胞器的清除,导致细胞损伤。在红细胞的成熟过程中,自噬不能清除细胞细胞器会干扰红细胞的正常分化,导致一系列疾病,如贫血。

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