Cargando…
Dysfunctional oxidative phosphorylation shunts branched‐chain amino acid catabolism onto lipogenesis in skeletal muscle
It is controversial whether mitochondrial dysfunction in skeletal muscle is the cause or consequence of metabolic disorders. Herein, we demonstrate that in vivo inhibition of mitochondrial ATP synthase in muscle alters whole‐body lipid homeostasis. Mice with restrained mitochondrial ATP synthase act...
Autores principales: | Sánchez‐González, Cristina, Nuevo‐Tapioles, Cristina, Herrero Martín, Juan Cruz, Pereira, Marta P, Serrano Sanz, Sandra, Ramírez de Molina, Ana, Cuezva, José M, Formentini, Laura |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360968/ https://www.ncbi.nlm.nih.gov/pubmed/32488939 http://dx.doi.org/10.15252/embj.2019103812 |
Ejemplares similares
-
Branched chain amino acid catabolism fuels adipocyte differentiation and lipogenesis
por: Green, Courtney R., et al.
Publicado: (2015) -
Coordinate β-adrenergic inhibition of mitochondrial activity and angiogenesis arrest tumor growth
por: Nuevo-Tapioles, Cristina, et al.
Publicado: (2020) -
Regulation of the H(+)-ATP synthase by IF1: a role in mitohormesis
por: Esparza-Moltó, Pau B., et al.
Publicado: (2017) -
Branched-chain Amino Acids: Catabolism in Skeletal Muscle and Implications for Muscle and Whole-body Metabolism
por: Mann, Gagandeep, et al.
Publicado: (2021) -
IF1 promotes oligomeric assemblies of sluggish ATP synthase and outlines the heterogeneity of the mitochondrial membrane potential
por: Romero-Carramiñana, Inés, et al.
Publicado: (2023)