| Literature DB >> 34716768 |
Kewal Kumar Mahapatra1, Soumya Ranjan Mishra1, Bishnu Prasad Behera1, Shankargouda Patil2, David A Gewirtz3, Sujit Kumar Bhutia4.
Abstract
Lysosomes are single membrane-bound organelles containing acid hydrolases responsible for the degradation of cellular cargo and maintenance of cellular homeostasis. Lysosomes could originate from pre-existing endolysosomes or autolysosomes, acting as a critical juncture between autophagy and endocytosis. Stress that triggers lysosomal membrane permeabilization can be altered by ESCRT complexes; however, irreparable damage to the membrane results in the induction of a selective lysosomal degradation pathway, specifically lysophagy. Lysosomes play an indispensable role in different types of autophagy, including microautophagy, macroautophagy, and chaperone-mediated autophagy, and various cell death pathways such as lysosomal cell death, apoptotic cell death, and autophagic cell death. In this review, we discuss lysosomal reformation, maintenance, and degradation pathways following the involvement of the lysosome in autophagy and cell death, which are related to several pathophysiological conditions observed in humans.Entities:
Keywords: Autolysosome; Autophagic cell death; Autophagic lysosome reformation; Autophagy; Lysosome
Mesh:
Year: 2021 PMID: 34716768 DOI: 10.1007/s00018-021-03988-3
Source DB: PubMed Journal: Cell Mol Life Sci ISSN: 1420-682X Impact factor: 9.261