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Por favor, use este identificador para citar o enlazar a este item: http://hdl.handle.net/10261/167541
Título

AMPKα1-LDH pathway regulates muscle stem cell self-renewal by controlling metabolic homeostasis.

AutorTheret, Marine; Gsaier, Linda; Schaffer, Bethany; Juban, Gaëtan; Ben Larbi, Sabrina; Weiss-Gayet, Michèle; Bultot, Laurent; Collodet, Caterina; Foretz, Marc; Desplanches, Dominique; Sanz, Pascual ; Zang, Zizhao; Yang, Lin; Vial, Guillaume; Viollet, Benoit; Sakamoto, Kei; Brunet, Anne; Chazaud, Bénédicte; Mounier, Rémi
Palabras claveGlycolysis
Metabolic shift
Skeletal muscle regeneration
Stem cell fate
Fecha de publicación3-jul-2017
EditorEMBO Press
CitaciónEMBO Journal 36(13):1946-1962 (2017)
ResumenControl of stem cell fate to either enter terminal differentiation versus returning to quiescence (self-renewal) is crucial for tissue repair. Here, we showed that AMP-activated protein kinase (AMPK), the master metabolic regulator of the cell, controls muscle stem cell (MuSC) self-renewal. AMPKα1-/- MuSCs displayed a high self-renewal rate, which impairs muscle regeneration. AMPKα1-/- MuSCs showed a Warburg-like switch of their metabolism to higher glycolysis. We identified lactate dehydrogenase (LDH) as a new functional target of AMPKα1. LDH, which is a non-limiting enzyme of glycolysis in differentiated cells, was tightly regulated in stem cells. In functional experiments, LDH overexpression phenocopied AMPKα1-/- phenotype, that is shifted MuSC metabolism toward glycolysis triggering their return to quiescence, while inhibition of LDH activity rescued AMPKα1-/- MuSC self-renewal. Finally, providing specific nutrients (galactose/glucose) to MuSCs directly controlled their fate through the AMPKα1/LDH pathway, emphasizing the importance of metabolism in stem cell fate.
Descripción17 Pages, 5 figures
Versión del editorhttp://dx.doi.org/10.15252/embj.201695273
URIhttp://hdl.handle.net/10261/167541
DOI10.15252/embj.201695273
ISSN0261-4189
E-ISSN1460-2075
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