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.

HDAC8 regulates canonical Wnt pathway to promote differentiation in skeletal muscles / L. Ferrari, C. Bragato, L. Brioschi, M. Spreafico, S. Esposito, A. Pezzotta, F. Pizzetti, A. Moreno-Fortuny, G. Bellipanni, A. Giordano, P. Riva, F. Frabetti, P. Viani, G. Cossu, M. Mora, A. Marozzi, A. Pistocchi. - In: JOURNAL OF CELLULAR PHYSIOLOGY. - ISSN 0021-9541. - 234:5(2019 May), pp. 6067-6076.

HDAC8 regulates canonical Wnt pathway to promote differentiation in skeletal muscles

L. Ferrari
Primo
;
L. Brioschi;M. Spreafico;A. Pezzotta;P. Riva;P. Viani;A. Marozzi
Penultimo
;
A. Pistocchi
Ultimo
2019

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.
histone deacetylase 8 (HDAC8); rhabdomyosarcoma; skeletal muscle; Wnt; zebrafish; physiology; clinical biochemistry; cell biology
Settore BIO/13 - Biologia Applicata
mag-2019
24-set-2018
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/597407
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