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Our research has revealed that the maintenance of proper mitochondrial-associated endoplasmic reticulum membranes (MAM) is vital for preventing skeletal muscle atrophy in microgravity environments. We discovered that the deletion of the mitochondrial fusion protein Mitofusin2 (MFN2), which serves as a tether for MAM, in human induced pluripotent stem (iPS) cells or the reduction of MAM in differentiated myotubes caused by microgravity interfered with myogenic differentiation process and an increased susceptibility to muscle atrophy, as well as the activation of the Notch signaling pathway. The atrophic phenotype of differentiated myotubes in microgravity and the regenerative capacity of Mfn2-deficient muscle stem cells in dystrophic mice were both ameliorated by treatment with the gamma-secretase inhibitor DAPT. Our findings demonstrate how the orchestration of mitochondrial morphology in differentiated myotubes and regenerating muscle stem cells plays a crucial role in regulating Notch signaling through the interaction of MAM.<\/jats:p>","DOI":"10.7554\/elife.89381","type":"journal-article","created":{"date-parts":[[2023,8,25]],"date-time":"2023-08-25T07:14:19Z","timestamp":1692947659000},"update-policy":"https:\/\/doi.org\/10.7554\/elife.89381","source":"Crossref","is-referenced-by-count":14,"title":["The reciprocal regulation between mitochondrial-associated membranes and Notch signaling in skeletal muscle atrophy"],"prefix":"10.7554","volume":"12","author":[{"given":"Yurika","family":"Ito","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/046f6cx68","id-type":"ROR","asserted-by":"publisher"}],"name":"Faculty of Medical Sciences, Fujita Health University","place":["Toyoake, 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