Blockade of Hemichannels Normalizes the Differentiation Fate of Myoblasts and Features of Skeletal Muscles from Dysferlin-Deficient Mice

Dysferlinopathies are muscle dystrophies caused by mutations in the gene encoding dysferlin, a relevant protein for membrane repair and trafficking. These diseases are untreatable, possibly due to the poor knowledge of relevant molecular targets. Previously, we have shown that human myofibers from p...

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Détails bibliographiques
Auteurs principaux: Luis A. Cea, Gabriela Fernández, Guisselle Arias-Bravo, Mario Castillo-Ruiz, Rosalba Escamilla, María C. Brañes, Juan C. Sáez
Format: Artigo
Langue:Inglês
Publié: MDPI AG 2020-08-01
Collection:International Journal of Molecular Sciences
Sujets:
PPARγ
lipid accumulation
connexons
sarcolemma permeability
hemichannel blocker
creatine kinase
Accès en ligne:https://www.mdpi.com/1422-0067/21/17/6025
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