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CHD4 ensures stem cell lineage fidelity during skeletal muscle regeneration

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Sreenivasan,  Krishnamoorthy
Cardiac Development and Remodeling, Max Planck Institute for Heart and Lung Research, Max Planck Society;

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Kim,  Johnny
Cardiac Development and Remodeling, Max Planck Institute for Heart and Lung Research, Max Planck Society;

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Ianni,  Alessandro
Cardiac Development and Remodeling, Max Planck Institute for Heart and Lung Research, Max Planck Society;

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Di Croce,  Luciano
Cardiac Development and Remodeling, Max Planck Institute for Heart and Lung Research, Max Planck Society;

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Braun,  Thomas
Cardiac Development and Remodeling, Max Planck Institute for Heart and Lung Research, Max Planck Society;

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Citation

Sreenivasan, K., Rodriguez-delaRosa, A., Kim, J., Mesquita, D., Segales, J., Gomez-del Arco, P., et al. (2021). CHD4 ensures stem cell lineage fidelity during skeletal muscle regeneration. STEM CELL REPORTS, 16(9), 2089-2098. doi:10.1016/j.stemcr.2021.07.022.


Cite as: https://hdl.handle.net/21.11116/0000-0009-49BC-2
Abstract
Regeneration of skeletal muscle requires resident stem cells called satellite cells. Here, we report that the chromatin remodeler CHD4, a member of the nucleosome remodeling and deacetylase (NuRD) repressive complex, is essential for the expansion and regenerative functions of satellite cells. We show that conditional deletion of the Chd4 gene in satellite cells results in failure to regenerate muscle after injury. This defect is principally associated with increased stem cell plasticity and lineage infidelity during the expansion of satellite cells, caused by de-repression of non-muscle-cell lineage genes in the absence of Chd4. Thus, CHD4 ensures that a transcriptional program that safeguards satellite cell identity during muscle regeneration is maintained. Given the therapeutic potential of muscle stem cells in diverse neuromuscular pathologies, CHD4 constitutes an attractive target for satellite cell-based therapies.