CHD4 ensures stem cell lineage fidelity during skeletal muscle regeneration

Stem Cell Reports. 2021 Sep 14;16(9):2089-2098. doi: 10.1016/j.stemcr.2021.07.022. Epub 2021 Aug 26.

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.

Keywords: Chd4; NuRD; lineage maintenance; muscle stem cell; regeneration; satellite cells; skeletal muscle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / genetics*
  • Cell Lineage / genetics*
  • Computational Biology
  • DNA Helicases / genetics*
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex / metabolism
  • Mice
  • Models, Biological
  • Muscle, Skeletal / physiology*
  • Regeneration*
  • Satellite Cells, Skeletal Muscle / cytology
  • Satellite Cells, Skeletal Muscle / metabolism
  • Stem Cells / cytology*
  • Stem Cells / metabolism*

Substances

  • Mi-2 Nucleosome Remodeling and Deacetylase Complex
  • Mi-2beta protein, mouse
  • DNA Helicases