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Persistent mdx diaphragm alterations are accompanied by increased expression and activity of calcium and muscle-specific proteins

    1. [1] Universidade Federal Fluminense

      Universidade Federal Fluminense

      Brasil

    2. [2] Universidade Federal do Rio de Janeiro

      Universidade Federal do Rio de Janeiro

      Brasil

  • Localización: Histology and histopathology: cellular and molecular biology, ISSN-e 1699-5848, ISSN 0213-3911, Vol. 36, Nº. 7, 2021, págs. 775-783
  • Idioma: inglés
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  • Resumen
    • The mdx mouse model of Duchenne Muscular Dystrophy (DMD) presents sarcolemma instability and develops a mild multi-stage dystrophinopathy characterized by intense myonecrosis with inflammatory infiltrate at 4-weeks; muscular regeneration at 12-weeks and persistent fibrosis onwards. Mdx diaphragm muscle has a more severe phenotype with structural and functional deterioration that closely resembles the diaphragm impairment responsible for DMD human patients' morbidity. Herein, we compared calcium deposits, activity of calciumrelated proteases, and expression of muscle-specific proteins in mdx diaphragm at 4-weeks and 12-weeks.

      We found increased calcium deposits mainly at 12- weeks, concomitant with high activity of calpains and matrix metalloprotease-9, but decreased expression of Myh4 (Myhc IIb) and Atp2a1 (SERCA1), and high expression of the myogenic regulatory factors Myod1 and Myog. Our results suggest that increased calcium deposits and persistent activity of calcium dependent proteases throughout the disease are involved in the degeneration and regeneration processes in the mdx diaphragm.


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