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Alliance"],"accepted":{"date-parts":[[2024,9,13]]},"published-print":{"date-parts":[[2024,12]]},"abstract":"<jats:p>\n                    LAMA2, coding for the laminin-\u03b12 chain, is a crucial ECM component, particularly abundant in skeletal muscle. Mutations in\n                    <jats:italic>LAMA2<\/jats:italic>\n                    trigger the often-lethal\n                    <jats:italic>LAMA2<\/jats:italic>\n                    -congenital muscular dystrophy (LAMA2-CMD). Various phenotypes have been linked to LAMA2-CMD; nevertheless, the precise mechanisms that malfunction during disease onset in utero remain unknown. We generated\n                    <jats:italic>Lama2<\/jats:italic>\n                    -deficient C2C12 cells and found that\n                    <jats:italic>Lama2<\/jats:italic>\n                    -deficient myoblasts display proliferation, differentiation, and fusion defects, DNA damage, oxidative stress, and mitochondrial dysfunction. Moreover, fetal myoblasts isolated from the\n                    <jats:italic>dy<\/jats:italic>\n                    <jats:sup>\n                      <jats:italic>W<\/jats:italic>\n                    <\/jats:sup>\n                    mouse model of LAMA2-CMD display impaired differentiation and fusion in vitro. We also showed that disease onset during fetal development is characterized by a significant down-regulation of gene expression in muscle fibers, causing pronounced effects on cytoskeletal organization, muscle differentiation, and altered DNA repair and oxidative stress responses. Together, our findings provide unique insights into the critical importance of the laminin-\u03b12 chain for muscle differentiation and muscle cell homeostasis.\n                  <\/jats:p>","DOI":"10.26508\/lsa.202402829","type":"journal-article","created":{"date-parts":[[2024,10,8]],"date-time":"2024-10-08T09:40:22Z","timestamp":1728380422000},"page":"e202402829","update-policy":"https:\/\/doi.org\/10.26508\/lsa.crossmarkpolicy","source":"Crossref","is-referenced-by-count":9,"title":["Laminin-\u03b12 chain deficiency in skeletal muscle causes dysregulation of multiple cellular mechanisms"],"prefix":"10.26508","volume":"7","author":[{"given":"Susana G","family":"Martins","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01c27hj86","id-type":"ROR","asserted-by":"publisher"}],"name":"Centre for Ecology, Evolution and Environmental Changes (CE3C) & CHANGE, Faculdade de Ci\u00eancias, Universidade de Lisboa","place":[", Lisboa, 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