Cargando…

A PGC1α-dependent myokine that drives browning of white fat and thermogenesis

Exercise benefits a variety of organ systems in mammals, and some of the best-recognized effects of exercise on muscle are mediated by the transcriptional coactivator PGC1α Here we show that PGC1α expression in muscle stimulates an increase in expression of Fndc5, a membrane protein that is cleaved...

Descripción completa

Detalles Bibliográficos
Autores principales: Boström, Pontus, Wu, Jun, Jedrychowski, Mark P., Korde, Anisha, Ye, Li, Lo, James C., Rasbach, Kyle A., Boström, Elisabeth Almer, Choi, Jang Hyun, Long, Jonathan Z., Kajimura, Shingo, Zingaretti, Maria Cristina, Vind, Birgitte F., Tu, Hua, Cinti, Saverio, Højlund, Kurt, Gygi, Steven P., Spiegelman, Bruce M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522098/
https://www.ncbi.nlm.nih.gov/pubmed/22237023
http://dx.doi.org/10.1038/nature10777
Descripción
Sumario:Exercise benefits a variety of organ systems in mammals, and some of the best-recognized effects of exercise on muscle are mediated by the transcriptional coactivator PGC1α Here we show that PGC1α expression in muscle stimulates an increase in expression of Fndc5, a membrane protein that is cleaved and secreted as a new hormone, irisin. Irisin acts on white adipose cells in culture and in vivo to stimulate UCP1 expression and a broad program of brown fat-like development. Irisin is induced with exercise in mice and humans, and mildly increased irisin levels in blood cause an increase in energy expenditure in mice with no changes in movement or food intake. This results in improvements in obesity and glucose homeostasis. Irisin could be a protein therapeutic for human metabolic disease and other disorders that are improved with exercise.