State Key Laboratory of Membrane Biology, Tsinghua University-Peking University Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China.
Mol Cells. 2018 Jan 31;41(1):45-49. doi: 10.14348/molcells.2018.2265. Epub 2018 Jan 23.
Autophagy is a lysosome-dependent degradation process that is essential for maintaining cellular homeostasis. In recent years, more studies have focused on the late stages of autophagy. Our group discovered and studied the terminal step of autophagy, namely autophagic lysosome reformation (ALR). ALR is the process that regenerates functional lysosomes from autolysosomes, thus maintaining lysosome homeostasis. ALR involves clathrin-mediated membrane budding from autolysosomes, elongation of membrane tubules along microtubules with the pulling force provided by the motor protein KIF5B, proto-lysosome scission by dynamin 2, and finally maturation of proto-lysosomes to functional lysosomes. In this review, we will summarize progress in unveiling the molecular mechanisms underlying ALR and its potential pathophysiological roles.
自噬是一种溶酶体依赖性的降解过程,对于维持细胞内稳态至关重要。近年来,越来越多的研究集中在自噬的晚期阶段。我们小组发现并研究了自噬的终末步骤,即自噬溶酶体再形成(ALR)。ALR 是从自噬溶酶体中再生功能性溶酶体的过程,从而维持溶酶体的稳态。ALR 涉及到网格蛋白介导的自噬溶酶体膜出芽、微管上的膜管沿着微管延伸,由动力蛋白 KIF5B 提供拉力、动力蛋白 2 介导的前溶酶体分裂,最后前溶酶体成熟为功能性溶酶体。在这篇综述中,我们将总结揭示 ALR 及其潜在病理生理作用的分子机制的进展。