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Not young but still immature: a HIF-1α–mediated maturation checkpoint in regenerating muscle
Rahagir Salekeen, Michael Kyba
Rahagir Salekeen, Michael Kyba
Published December 1, 2022
Citation Information: J Clin Invest. 2022;132(23):e165322. https://doi.org/10.1172/JCI165322.
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Commentary

Not young but still immature: a HIF-1α–mediated maturation checkpoint in regenerating muscle

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Abstract

Muscle fibers express particular isoforms of contractile proteins, depending on the fiber’s function and the organism’s developmental stage. In the adult, after a muscle injury, newly generated fibers transition through embryonic and neonatal myosins, prior to selecting their distinctive adult myosin isoform. In this issue of the JCI, Wang et al. discover a checkpoint that regulates the neonatal-to-adult myosin isoform transition. They found that HIF-1α regulated this checkpoint, with elevated HIF-1α levels blocking progression, while HIF-1α knockout accelerated the transition. They further related these findings to centronuclear myopathy, a disease in which HIF-1α is similarly elevated and neonatal myosin expression is maintained. These findings highlight a maturation checkpoint that impacts the skeletal muscle regeneration following ischemic injury, providing a pharmacologically accessible pathway in injury and diseases such as centronuclear myopathy.

Authors

Rahagir Salekeen, Michael Kyba

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Figure 1

HIF-1α serves as a maturation checkpoint during muscle regeneration after injury.

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HIF-1α serves as a maturation checkpoint during muscle regeneration afte...
Following injury, newly formed fibers mirror embryonic muscle development, initially expressing embryonic myosin heavy chain (MYH3, blue), and then switching to neonatal myosin (MYH8, yellow) before finally expressing definitive adult myosins appropriate to their particular fiber type (red and purple). MFN2-depleted animals exhibit a maturation arrest phenotype at the neonatal myosin (MYH8+) stage. This arrest resembles the pathological phenotype in centronuclear myopathy (shown below). In both cases, prolonged fetal myosin expression is associated with sustained expression of HIF-1α, which serves as a maturation checkpoint.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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