Department of Pharmacology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Department of Pharmacology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Int Rev Cell Mol Biol. 2020;352:159-187. doi: 10.1016/bs.ircmb.2019.12.004. Epub 2020 Jan 13.
Autophagy, the process of macromolecular degradation through the lysosome, has been extensively studied for the past decade or two. Autophagy can regulate cell death, especially apoptosis, through selective degradation of both positive and negative apoptosis regulators. However, multiple other programmed cell death pathways exist. As knowledge of these other types of cell death expand, it has been suggested that they also interact with autophagy. In this review, we discuss the molecular mechanisms that comprise three non-apoptotic forms of cell death (necroptosis, pyroptosis and ferroptosis) focusing on how the autophagy machinery regulates these different cell death mechanisms through (i) its degradative functions, i.e., true autophagy, and (ii) other non-degradative functions of the autophagy machinery such as serving as a signaling scaffold or by participating in other autophagy-independent cellular processes.
自噬,即通过溶酶体进行大分子降解的过程,在过去的一二十年里得到了广泛的研究。自噬可以通过选择性降解正、负凋亡调节剂来调节细胞死亡,特别是细胞凋亡。然而,还存在多种其他程序性细胞死亡途径。随着对这些其他类型细胞死亡的认识的扩展,人们认为它们也与自噬相互作用。在这篇综述中,我们讨论了构成三种非凋亡细胞死亡形式(坏死性凋亡、细胞焦亡和铁死亡)的分子机制,重点讨论了自噬机制如何通过(i)其降解功能,即真正的自噬,和(ii)自噬机制的其他非降解功能,如作为信号支架或参与其他非自噬的细胞过程,来调节这些不同的细胞死亡机制。