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J Cell Biol. 2012 Sep 3;198(5):815-32. doi: 10.1083/jcb.201201050.

Six1 regulates stem cell repair potential and self-renewal during skeletal muscle regeneration.

Author information

1
Institut National de la Santé et de la Recherche Médicale U1016, Institut Cochin, Paris 75014, France. fabien.le-grand@inserm.fr

Abstract

Satellite cells (SCs) are stem cells that mediate skeletal muscle growth and regeneration. Here, we observe that adult quiescent SCs and their activated descendants expressed the homeodomain transcription factor Six1. Genetic disruption of Six1 specifically in adult SCs impaired myogenic cell differentiation, impaired myofiber repair during regeneration, and perturbed homeostasis of the stem cell niche, as indicated by an increase in SC self-renewal. Six1 regulated the expression of the myogenic regulatory factors MyoD and Myogenin, but not Myf5, which suggests that Six1 acts on divergent genetic networks in the embryo and in the adult. Moreover, we demonstrate that Six1 regulates the extracellular signal-regulated kinase 1/2 (ERK1/2) pathway during regeneration via direct control of Dusp6 transcription. Muscles lacking Dusp6 were able to regenerate properly but showed a marked increase in SC number after regeneration. We conclude that Six1 homeoproteins act as a rheostat system to ensure proper regeneration of the tissue and replenishment of the stem cell pool during the events that follow skeletal muscle trauma.

PMID:
22945933
PMCID:
PMC3432771
DOI:
10.1083/jcb.201201050
[Indexed for MEDLINE]
Free PMC Article

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