| Literature DB >> 30246374 |
Luca Ferrari1, Cinzia Bragato2,3, Loredana Brioschi1, Marco Spreafico1, Simona Esposito1, Alex Pezzotta1, Fabrizio Pizzetti4, Artal Moreno-Fortuny5,6, Gianfranco Bellipanni7, Antonio Giordano7,8, Paola Riva1, Flavia Frabetti4, Paola Viani1, Giulio Cossu5, Marina Mora2, Anna Marozzi1, Anna Pistocchi1.
Abstract
Histone deacetylase 8 (HDAC8) is a class 1 histone deacetylase and a member of the cohesin complex. HDAC8 is expressed in smooth muscles, but its expression in skeletal muscle has not been described. We have shown for the first time that HDAC8 is expressed in human and zebrafish skeletal muscles. Using RD/12 and RD/18 rhabdomyosarcoma cells with low and high differentiation potency, respectively, we highlighted a specific correlation with HDAC8 expression and an advanced stage of muscle differentiation. We inhibited HDAC8 activity through a specific PCI-34051 inhibitor in murine C2C12 myoblasts and zebrafish embryos, and we observed skeletal muscles differentiation impairment. We also found a positive regulation of the canonical Wnt signaling by HDAC8 that might explain muscle differentiation defects. These findings suggest a novel mechanism through which HDAC8 expression, in a specific time window of skeletal muscle development, positively regulates canonical Wnt pathway that is necessary for muscle differentiation.Entities:
Keywords: Wnt; histone deacetylase 8 (HDAC8); rhabdomyosarcoma; skeletal muscle; zebrafish
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Year: 2018 PMID: 30246374 DOI: 10.1002/jcp.27341
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384