HDAC4 regulates satellite cell proliferation and differentiation by targeting P21 and Sharp1 genes

Valentina Saccone, Sara Consalvi, Nicoletta Marroncelli, Marco Bertin, Silvia Consalvi, Marco De Bardi, Pier Lorenzo Puri, Daniela Palacios, Sergio Adamo, Viviana Moresi

Risultato della ricerca: Contributo in rivistaArticolo in rivista

16 Citazioni (Scopus)

Abstract

Skeletal muscle exhibits a high regenerative capacity, mainly due to the ability of satellite cells to replicate and differentiate in response to appropriate stimuli. Epigenetic control is effective at different stages of this process. It has been shown that the chromatin-remodeling factor HDAC4 is able to regulate satellite cell proliferation and commitment. However, its molecular targets are still uncovered. To explain the signaling pathways regulated by HDAC4 in satellite cells, we generated tamoxifen-inducible mice with conditional inactivation of HDAC4 in Pax7+ cells (HDAC4 KO mice). We found that the proliferation and differentiation of HDAC4 KO satellite cells were compromised, although similar amounts of satellite cells were found in mice. Moreover, we found that the inhibition of HDAC4 in satellite cells was sufficient to block the differentiation process. By RNA-sequencing analysis we identified P21 and Sharp1 as HDAC4 target genes. Reducing the expression of these target genes in HDAC4 KO satellite cells, we also defined the molecular pathways regulated by HDAC4 in the epigenetic control of satellite cell expansion and fusion.
Lingua originaleEnglish
pagine (da-a)3448-N/A
RivistaScientific Reports
Volume8
DOI
Stato di pubblicazionePubblicato - 2018

Keywords

  • Animals
  • Cell Differentiation
  • Cell Proliferation
  • Cells, Cultured
  • Cyclin-Dependent Kinase Inhibitor p21
  • Epigenesis, Genetic
  • Histone Deacetylases
  • Mice
  • Mice, Knockout
  • PAX7 Transcription Factor
  • Satellite Cells, Skeletal Muscle
  • Signal Transduction
  • Tamoxifen
  • Transcription Factors

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