<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>107(42)</volume><submitter>Guo P</submitter><pubmed_abstract>Phagocytosis of apoptotic cells requires recognition of cell corpses followed by internalization and enclosure within plasma membrane-derived phagosomes. Phagosomes undergo maturation to generate phagolysosomes in which cell corpses are degraded; however, regulation of the maturation process is poorly understood. Here, we identified Rab GTPase 14, which regulates apoptotic cell degradation in Caenorhabditis elegans. rab-14 mutants accumulate many persistent cell corpses owing to defective cell corpse clearance. Loss of rab-14 function affects several steps of phagosome maturation including phagosomal acidification and phagolysosome formation. RAB-14 and UNC-108/RAB2 are recruited to phagosomes at a similar stage and function redundantly to regulate phagosome maturation. Three Rabs, RAB-14, UNC-108/RAB2, and RAB-7, act in sequential steps to control phagolysosome formation. RAB-14 and UNC-108 recruit lysosomes, whereas RAB-7 mediates fusion of lysosomes to phagosomes. Our data reveal the sequential action of Rab GTPases in regulating tethering, docking, and fusion of lysosomes to apoptotic cell-containing phagosomes.</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>18016-21</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2964220</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Sequential action of Caenorhabditis elegans Rab GTPases regulates phagolysosome formation during apoptotic cell degradation.</pubmed_title><pmcid>PMC2964220</pmcid><pubmed_authors>Hu T</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Jiang S</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Guo P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sequential action of Caenorhabditis elegans Rab GTPases regulates phagolysosome formation during apoptotic cell degradation.</name><description>Phagocytosis of apoptotic cells requires recognition of cell corpses followed by internalization and enclosure within plasma membrane-derived phagosomes. Phagosomes undergo maturation to generate phagolysosomes in which cell corpses are degraded; however, regulation of the maturation process is poorly understood. Here, we identified Rab GTPase 14, which regulates apoptotic cell degradation in Caenorhabditis elegans. rab-14 mutants accumulate many persistent cell corpses owing to defective cell corpse clearance. Loss of rab-14 function affects several steps of phagosome maturation including phagosomal acidification and phagolysosome formation. RAB-14 and UNC-108/RAB2 are recruited to phagosomes at a similar stage and function redundantly to regulate phagosome maturation. Three Rabs, RAB-14, UNC-108/RAB2, and RAB-7, act in sequential steps to control phagolysosome formation. RAB-14 and UNC-108 recruit lysosomes, whereas RAB-7 mediates fusion of lysosomes to phagosomes. Our data reveal the sequential action of Rab GTPases in regulating tethering, docking, and fusion of lysosomes to apoptotic cell-containing phagosomes.</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Oct</publication><modification>2025-04-26T11:25:06.203Z</modification><creation>2019-03-27T00:35:08Z</creation></dates><accession>S-EPMC2964220</accession><cross_references><pubmed>20921409</pubmed><doi>10.1073/pnas.1008946107</doi></cross_references></HashMap>