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However, how endolysosomal dysfunction causes musculoskeletal abnormalities remains poorly understood, limiting therapeutic options. Here, we report that CHMP5, a member of the endosomal sorting complex required for transport (ESCRT)-III protein family, is essential to maintain the endolysosomal pathway and regulate bone formation in osteogenic lineage cells. Genetic ablation of\n                    <jats:italic>Chmp5<\/jats:italic>\n                    in mouse osteogenic cells increases bone formation in vivo and in vitro. Mechanistically,\n                    <jats:italic>Chmp5<\/jats:italic>\n                    deletion causes endolysosomal dysfunction by decreasing the VPS4A protein, and CHMP5 overexpression is sufficient to increase the VPS4A protein. Subsequently, endolysosomal dysfunction disturbs mitochondrial functions and increases mitochondrial ROS, ultimately resulting in skeletal cell senescence. Senescent skeletal cells cause abnormal bone formation by combining cell-autonomous and paracrine actions. Importantly, the elimination of senescent cells using senolytic drugs can alleviate musculoskeletal abnormalities in\n                    <jats:italic>Chmp5<\/jats:italic>\n                    conditional knockout mice. Therefore, our results show that cell senescence represents an underpinning mechanism and a therapeutic target for musculoskeletal disorders caused by the aberrant endolysosomal pathway, such as in lysosomal storage diseases. These results also uncover the function and mechanism of CHMP5 in the regulation of cell senescence by affecting the endolysosomal-mitochondrial pathway.\n                  <\/jats:p>","DOI":"10.7554\/elife.101984","type":"journal-article","created":{"date-parts":[[2024,11,19]],"date-time":"2024-11-19T05:25:20Z","timestamp":1731993920000},"update-policy":"https:\/\/doi.org\/10.7554\/elife.101984","source":"Crossref","is-referenced-by-count":2,"title":["The ESCRT protein CHMP5 restricts bone formation by controlling endolysosome-mitochondrion-mediated cell senescence"],"prefix":"10.7554","volume":"13","author":[{"ORCID":"https:\/\/orcid.org\/0009-0006-6245-0199","authenticated-orcid":true,"given":"Fan","family":"Zhang","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/00k7r7f88","id-type":"ROR","asserted-by":"publisher"}],"name":"Xuanwu Hospital Capital Medical University","place":["Beijing, China"]},{"name":"National Clinical Research Center for Geriatric Diseases","place":["Beijing, China"]},{"name":"Joint Therapeutics Co. 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