<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Klein AD</submitter><funding>NCI NIH HHS</funding><pagination>ar70</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11151102</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>35(5)</volume><pubmed_abstract>Lysosome turnover and biogenesis are induced in response to treatment of cells with agents that cause membrane rupture, but whether other stress conditions engage similar homeostatic mechanisms is not well understood. Recently we described a form of selective turnover of lysosomes that is induced by metabolic stress or by treatment of cells with ionophores or lysosomotropic agents, involving the formation of intraluminal vesicles within intact organelles through microautophagy. Selective turnover involves noncanonical autophagy and the lipidation of LC3 onto lysosomal membranes, as well as the autophagy gene-dependent formation of intraluminal vesicles. Here, we find a form of microautophagy induction that requires activity of the lipid kinase PIKfyve and is associated with the nuclear tra</pubmed_abstract><journal>Molecular biology of the cell</journal><pubmed_title>Stress-induced microautophagy is coordinated with lysosome biogenesis and regulated by PIKfyve.</pubmed_title><pmcid>PMC11151102</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>R35 CA263846</funding_grant_id><pubmed_authors>Lee C</pubmed_authors><pubmed_authors>Petruzzi KL</pubmed_authors><pubmed_authors>Klein AD</pubmed_authors><pubmed_authors>Overholtzer M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Stress-induced microautophagy is coordinated with lysosome biogenesis and regulated by PIKfyve.</name><description>Lysosome turnover and biogenesis are induced in response to treatment of cells with agents that cause membrane rupture, but whether other stress conditions engage similar homeostatic mechanisms is not well understood. Recently we described a form of selective turnover of lysosomes that is induced by metabolic stress or by treatment of cells with ionophores or lysosomotropic agents, involving the formation of intraluminal vesicles within intact organelles through microautophagy. Selective turnover involves noncanonical autophagy and the lipidation of LC3 onto lysosomal membranes, as well as the autophagy gene-dependent formation of intraluminal vesicles. Here, we find a form of microautophagy induction that requires activity of the lipid kinase PIKfyve and is associated with the nuclear tra</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-05-07T08:51:12.645Z</modification><creation>2026-04-07T22:40:03.538Z</creation></dates><accession>S-EPMC11151102</accession><cross_references><pubmed>38536415</pubmed><doi>10.1091/mbc.E23-08-0332</doi></cross_references></HashMap>