{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"submitter":["Kolli S"],"funding":["NIH HHS","NIGMS NIH HHS"],"pubmed_abstract":["Cell corpses must be cleared in an efficient manner to maintain tissue homeostasis and regulate immune responses. Ubiquitin-like Atg8/LC3 family proteins promote the degradation of membranes and internal cargo during both macroautophagy and corpse clearance, raising the question how macroautophagy contributes to corpse clearance. Studying the clearance of non-apoptotic dying polar bodies in <i>Caenorhabditis elegans</i> embryos, we show that the LC3 ortholog LGG-2 is enriched in the polar body phagolysosome independent of membrane association or autophagosome formation. We demonstrate that ATG-16.1 and ATG-16.2, which promote membrane association of lipidated Atg8/LC3 proteins, redundantly promote polar body membrane breakdown in phagolysosomes independent of their role in macroautophagy. We also show that the lipid scramblase ATG-9 is needed for autophagosome formation in early embryos but is dispensable for timely polar body membrane breakdown or protein cargo degradation. These findings demonstrate that macroautophagy is not required to promote polar body degradation, in contrast to recent findings with apoptotic corpse clearance in <i>C. elegans</i> embryos. Determining how membrane association of Atg8/LC3 promotes the breakdown of different types of cell corpses in distinct cell types or metabolic states is likely to give insights into the mechanisms of immunoregulation during normal development, physiology, and disease."],"journal":["bioRxiv : the preprint server for biology"],"pagination":["2024.06.19.599770"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11212964"],"repository":["biostudies-literature"],"pubmed_title":["Phagolysosomes break down the membrane of a non-apoptotic corpse independent of macroautophagy."],"pmcid":["PMC11212964"],"funding_grant_id":["R15 GM143727","P40 OD010440"],"pubmed_authors":["Wehman AM","Kolli S","Kline CJ","Rad KM"],"additional_accession":[]},"is_claimable":false,"name":"Phagolysosomes break down the membrane of a non-apoptotic corpse independent of macroautophagy.","description":"Cell corpses must be cleared in an efficient manner to maintain tissue homeostasis and regulate immune responses. Ubiquitin-like Atg8/LC3 family proteins promote the degradation of membranes and internal cargo during both macroautophagy and corpse clearance, raising the question how macroautophagy contributes to corpse clearance. Studying the clearance of non-apoptotic dying polar bodies in <i>Caenorhabditis elegans</i> embryos, we show that the LC3 ortholog LGG-2 is enriched in the polar body phagolysosome independent of membrane association or autophagosome formation. We demonstrate that ATG-16.1 and ATG-16.2, which promote membrane association of lipidated Atg8/LC3 proteins, redundantly promote polar body membrane breakdown in phagolysosomes independent of their role in macroautophagy. We also show that the lipid scramblase ATG-9 is needed for autophagosome formation in early embryos but is dispensable for timely polar body membrane breakdown or protein cargo degradation. These findings demonstrate that macroautophagy is not required to promote polar body degradation, in contrast to recent findings with apoptotic corpse clearance in <i>C. elegans</i> embryos. Determining how membrane association of Atg8/LC3 promotes the breakdown of different types of cell corpses in distinct cell types or metabolic states is likely to give insights into the mechanisms of immunoregulation during normal development, physiology, and disease.","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Jun","modification":"2025-04-22T12:08:41.736Z","creation":"2025-04-06T00:13:12.017Z"},"accession":"S-EPMC11212964","cross_references":{"pubmed":["38948720"],"doi":["10.1101/2024.06.19.599770"]}}