Department of Surgery, UT Southwestern Medical Center, Dallas, Texas, USA.
Life Sciences Institute and Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, Michigan, USA.
Autophagy. 2022 Jan;18(1):4-23. doi: 10.1080/15548627.2021.1885147. Epub 2021 Mar 3.
Ion exchange between intracellular and extracellular spaces is the basic mechanism for controlling cell metabolism and signal transduction. This process is mediated by ion channels and transporters on the plasma membrane, or intracellular membranes that surround various organelles, in response to environmental stimuli. Macroautophagy (hereafter referred to as autophagy) is one of the lysosomal-dependent degradation pathways that maintains homeostasis through the degradation and recycling of cellular components (e.g., dysfunctional proteins and damaged organelles). Although autophagy-related (ATG) proteins play a central role in regulating the formation of autophagy-related member structures (e.g., phagophores, autophagosomes, and autolysosomes), the autophagic process also involves changes in expression and function of ion channels and transporters. Here we discuss current knowledge of the mechanisms that regulate autophagy in mammalian cells, with special attention to the ion channels and transporters. We also highlight prospects for the development of drugs targeting ion channels and transporters in autophagy.
细胞内外离子交换是控制细胞代谢和信号转导的基本机制。该过程通过质膜或包围各种细胞器的细胞内膜上的离子通道和转运蛋白来介导,以响应环境刺激。巨自噬(以下简称自噬)是溶酶体依赖性降解途径之一,通过降解和回收细胞成分(例如,功能失调的蛋白质和受损的细胞器)来维持体内平衡。尽管自噬相关(ATG)蛋白在调节自噬相关成员结构(例如,吞噬体、自噬体和自溶酶体)的形成中起核心作用,但自噬过程还涉及离子通道和转运蛋白表达和功能的变化。在这里,我们讨论了调节哺乳动物细胞自噬的机制的最新知识,特别关注离子通道和转运蛋白。我们还强调了针对自噬中离子通道和转运蛋白的药物开发的前景。