Deficiency of MMP-10 Aggravates the Diseased Phenotype of Aged Dystrophic Mice

Matrix metalloproteinases (MMPs) have been implicated in the progression of muscular dystrophy, and recent studies have reported the role of MMP-10 in skeletal muscle pathology of young dystrophic mice. Nevertheless, its involvement in dystrophin-deficient hearts remains unexplored. Here, we aimed t...

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Veröffentlicht in:Life (Basel, Switzerland) Switzerland), 2021-12, Vol.11 (12), p.1398
Hauptverfasser: Baraibar-Churio, Arantxa, Bobadilla, Míriam, Machado, Florencio J D, Sáinz, Neira, Roncal, Carmen, Abizanda, Gloria, Prósper, Felipe, Orbe, Josune, Pérez-Ruiz, Ana
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Sprache:eng
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Zusammenfassung:Matrix metalloproteinases (MMPs) have been implicated in the progression of muscular dystrophy, and recent studies have reported the role of MMP-10 in skeletal muscle pathology of young dystrophic mice. Nevertheless, its involvement in dystrophin-deficient hearts remains unexplored. Here, we aimed to investigate the involvement of MMP-10 in the progression of severe muscular dystrophy and to characterize MMP-10 loss in skeletal and cardiac muscles of aged dystrophic mice. We examined the histopathological effect of MMP-10 ablation in aged mice, both in the hind limb muscles and heart tissues. We found that MMP-10 loss compromises survival rates of aged mice, with skeletal and cardiac muscles developing a chronic inflammatory response. Our findings indicate that MMP-10 is implicated in severe muscular dystrophy progression, thus identifying a new area of research that could lead to future therapies for dystrophic muscles.
ISSN:2075-1729
2075-1729
DOI:10.3390/life11121398