Key result
Loss of Cebpb expression in satellite cells resulted in precocious differentiation of myoblasts, greater cell fusion, larger muscle fiber cross-sectional area, and improved repair after injury.
C/EBPβ acts as a potent inhibitor of myogenic differentiation in satellite cells, and its downregulation is essential for effective muscle repair and myogenesis.
C/EBPβ inhibition may enhance satellite cell-mediated repair; leaves open translation to human muscle injury therapies.
Upon injury, muscle satellite cells become activated and produce skeletal muscle precursors that engage in myogenesis. We demonstrate that the transcription factor CCAAT/enhancer binding protein beta (C/EBPβ) is expressed in the satellite cells of healthy muscle. C/EBPβ expression is regulated during myogenesis such that C/EBPβ is rapidly and massively downregulated upon induction to differentiate. Furthermore, persistent expression of C/EBPβ in myoblasts potently inhibits differentiation at least in part through the inhibition of MyoD protein function and stability. As a consequence, myogenic factor expression, myosin heavy chain expression, and fusogenic activity were reduced in C/EBPβ-overexpressing cells. Using knockout models, we demonstrate that loss of Cebpb expression in satellite cells results in precocious differentiation of myoblasts in growth conditions and greater cell fusion upon differentiation. In vivo, loss of Cebpb expression in satellite cells resulted in larger muscle fiber cross-sectional area and improved repair after muscle injury. Our results support the notion that C/EBPβ inhibits myogenic differentiation and that its levels must be reduced to allow for activation of MyoD target genes and the progression of differentiation.
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Marchildon et al. (2012) studied Muscle injury and myogenesis. C/EBPβ overexpression or knockout vs. Wild-type or control cells/animals was evaluated on Myogenic differentiation, cell fusion, and muscle fiber cross-sectional area. Loss of Cebpb expression in satellite cells resulted in precocious differentiation of myoblasts, greater cell fusion, larger muscle fiber cross-sectional area, and improved repair after injury.
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