Your browser doesn't support javascript.
loading
A mitofusin 2/HIF1α axis sets a maturation checkpoint in regenerating skeletal muscle.
Wang, Xun; Jia, Yuemeng; Zhao, Jiawei; Lesner, Nicholas P; Menezes, Cameron J; Shelton, Spencer D; Venigalla, Siva Sai Krishna; Xu, Jian; Cai, Chunyu; Mishra, Prashant.
Afiliación
  • Wang X; Children's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
  • Jia Y; Children's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
  • Zhao J; Division of Hematology/Oncology, Boston Children's Hospital, Boston, Massachusetts, USA.
  • Lesner NP; Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, USA.
  • Menezes CJ; Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.
  • Shelton SD; Children's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
  • Venigalla SSK; Children's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
  • Xu J; Children's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
  • Cai C; Children's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
  • Mishra P; Children's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
J Clin Invest ; 132(23)2022 12 01.
Article en En | MEDLINE | ID: mdl-36125902
A fundamental issue in regenerative medicine is whether there exist endogenous regulatory mechanisms that limit the speed and efficiency of the repair process. We report the existence of a maturation checkpoint during muscle regeneration that pauses myofibers at a neonatal stage. This checkpoint is regulated by the mitochondrial protein mitofusin 2 (Mfn2), the expression of which is activated in response to muscle injury. Mfn2 is required for growth and maturation of regenerating myofibers; in the absence of Mfn2, new myofibers arrested at a neonatal stage, characterized by centrally nucleated myofibers and loss of H3K27me3 repressive marks at the neonatal myosin heavy chain gene. A similar arrest at the neonatal stage was observed in infantile cases of human centronuclear myopathy. Mechanistically, Mfn2 upregulation suppressed expression of hypoxia-induced factor 1α (HIF1α), which is induced in the setting of muscle damage. Sustained HIF1α signaling blocked maturation of new myofibers at the neonatal-to-adult fate transition, revealing the existence of a checkpoint that delays muscle regeneration. Correspondingly, inhibition of HIF1α allowed myofibers to bypass the checkpoint, thereby accelerating the repair process. We conclude that skeletal muscle contains a regenerative checkpoint that regulates the speed of myofiber maturation in response to Mfn2 and HIF1α activity.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Regeneración / Músculo Esquelético / Proteínas Mitocondriales / Subunidad alfa del Factor 1 Inducible por Hipoxia Límite: Humans / Newborn Idioma: En Revista: J Clin Invest Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Regeneración / Músculo Esquelético / Proteínas Mitocondriales / Subunidad alfa del Factor 1 Inducible por Hipoxia Límite: Humans / Newborn Idioma: En Revista: J Clin Invest Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos