Cargando…
Pharmacological inhibition of HDAC6 improves muscle phenotypes in dystrophin-deficient mice by downregulating TGF-β via Smad3 acetylation
The absence of dystrophin in Duchenne muscular dystrophy disrupts the dystrophin-associated glycoprotein complex resulting in skeletal muscle fiber fragility and atrophy, associated with fibrosis as well as microtubule and neuromuscular junction disorganization. The specific, non-conventional cytopl...
Autores principales: | Osseni, Alexis, Ravel-Chapuis, Aymeric, Belotti, Edwige, Scionti, Isabella, Gangloff, Yann-Gaël, Moncollin, Vincent, Mazelin, Laetitia, Mounier, Remi, Leblanc, Pascal, Jasmin, Bernard J., Schaeffer, Laurent |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675748/ https://www.ncbi.nlm.nih.gov/pubmed/36402791 http://dx.doi.org/10.1038/s41467-022-34831-3 |
Ejemplares similares
-
HDAC6 regulates microtubule stability and clustering of AChRs at neuromuscular junctions
por: Osseni, Alexis, et al.
Publicado: (2020) -
Lack of muscle mTOR kinase activity causes early onset myopathy and compromises whole‐body homeostasis
por: Zhang, Qing, et al.
Publicado: (2018) -
Muscle inactivation of mTOR causes metabolic and dystrophin defects leading to severe myopathy
por: Risson, Valérie, et al.
Publicado: (2009) -
H2A.Z is dispensable for both basal and activated transcription in post-mitotic mouse muscles
por: Belotti, Edwige, et al.
Publicado: (2020) -
The ESCRT-0 subcomplex component Hrs/Hgs is a master regulator of myogenesis via modulation of signaling and degradation pathways
por: Coudert, L., et al.
Publicado: (2021)