Department of Biochemistry & Molecular Biology, Graduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan 33302, Taiwan.
Liver Research Center, Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan.
Cells. 2024 Mar 13;13(6):500. doi: 10.3390/cells13060500.
In eukaryotes, targeting intracellular components for lysosomal degradation by autophagy represents a catabolic process that evolutionarily regulates cellular homeostasis. The successful completion of autophagy initiates the engulfment of cytoplasmic materials within double-membrane autophagosomes and subsequent delivery to autolysosomes for degradation by acidic proteases. The formation of autolysosomes relies on the precise fusion of autophagosomes with lysosomes. In recent decades, numerous studies have provided insights into the molecular regulation of autophagosome-lysosome fusion. In this review, an overview of the molecules that function in the fusion of autophagosomes with lysosomes is provided. Moreover, the molecular mechanism underlying how these functional molecules regulate autophagosome-lysosome fusion is summarized.
在真核生物中,通过自噬将细胞内成分靶向到溶酶体降解是一种代谢过程,它可以进化调节细胞内的稳态。自噬的成功启动会导致双层膜自噬体吞噬细胞质物质,并随后将其递送至溶酶体,由酸性蛋白酶进行降解。自溶酶体的形成依赖于自噬体与溶酶体的精确融合。在过去的几十年中,大量的研究为我们提供了对自噬体-溶酶体融合的分子调控的深入了解。在这篇综述中,概述了参与自噬体与溶酶体融合的分子。此外,还总结了这些功能分子调节自噬体-溶酶体融合的分子机制。