Rosales, Xiomara Q.Malik, VinodSneh, AmitaChen, LeiLewis, SarahKota, JanaiahGastier-Foster, Julie M.Astbury, CarolinePyatt, RobReshmi, ShaliniRodino-Klapac, Louise R.Clark, K. ReedMendell, Jerry R.Sahenk, Zarife2020-01-102020-01-102013-05https://hdl.handle.net/1805/21814Introduction—Recent in vitro studies suggest that CAPN3 deficiency leads initially to accelerated myofiber formation followed by depletion of satellite cells (SC). In normal muscle, upregulation of miR-1 and miR-206 facilitates transition from proliferating SCs to differentiating myogenic progenitors. Methods—We examined the histopathological stages, Pax7 SC content, and muscle specific microRNA expression in biopsy specimens from well-characterized LGMD 2A patients to gain insight into disease pathogenesis. Results—Three distinct stages of pathological changes were identified that represented the continuum of the dystrophic process from prominent inflammation with necrosis and regeneration to prominent fibrosis, which correlated with age and disease duration. Pax7-positive SCs were highest in fibrotic group and correlated with down-regulation of miR-1, miR-133a, and miR-206. Conclusions—These observations, and other published reports, are consistent with microRNA dysregulation leading to inability of Pax7-positive SCs to transit from proliferation to differentiation. This results in impaired regeneration and fibrosis.LGMD2AFibrosismicroRNAmuscle regenerationArticle10.1002/mus.23669