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Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity

Authors :
Fabiola Moretti
Roberta Morosetti
Sabrina Sacconi
Enzo Ricci
Isabella Cascino
Marsha Pellegrino
Giancarlo Deidda
Giorgio Tasca
Giuliana Galluzzi
Marco Crescenzi
Alfredo Pontecorvi
Emanuela Teveroni
Angela Puma
Matteo Garibaldi
Carlo P. Trevisan
Stefano Farioli-Vecchioli
Patrizia Calandra
Source :
The Journal of clinical investigation (2017). doi:10.1172/JCI89401, info:cnr-pdr/source/autori:Teveroni, Emanuela; Pellegrino, Marsha; Sacconi, Sabrina; Calandra, Patrizia; Cascino, Isabella; Farioli-Vecchioli, Stefano; Puma, Angela; Garibaldi, Matteo; Morosetti, Roberta; Tasca, Giorgio; Ricci, Enzo; Trevisan, Carlo Pietro; Galluzzi, Giuliana; Pontecorvi, Alfredo; Crescenzi, Marco; Deidda, Giancarlo; Moretti, Fabiola/titolo:Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity./doi:10.1172%2FJCI89401/rivista:The Journal of clinical investigation/anno:2017/pagina_da:/pagina_a:/intervallo_pagine:/volume
Publication Year :
2016

Abstract

Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular disorder that is characterized by extreme variability in symptoms, with females being less severely affected than males and presenting a higher proportion of asymptomatic carriers. The sex-related factors involved in the disease are not known. Here, we have utilized myoblasts isolated from FSHD patients (FSHD myoblasts) to investigate the effect of estrogens on muscle properties. Our results demonstrated that estrogens counteract the differentiation impairment of FSHD myoblasts without affecting cell proliferation or survival. Estrogen effects are mediated by estrogen receptor beta (ERbeta), which reduces chromatin occupancy and transcriptional activity of double homeobox 4 (DUX4), a protein whose aberrant expression has been implicated in FSHD pathogenesis. During myoblast differentiation, we observed that the levels and activity of DUX4 increased progressively and were associated with its enhanced recruitment in the nucleus. ERbeta interfered with this recruitment by relocalizing DUX4 in the cytoplasm. This work identifies estrogens as a potential disease modifier that underlie sex-related differences in FSHD by protecting against myoblast differentiation impairments in this disease.

Details

ISSN :
15588238
Volume :
127
Issue :
4
Database :
OpenAIRE
Journal :
The Journal of clinical investigation
Accession number :
edsair.doi.dedup.....a616d11d1f1597c389f2467506c1d7da
Full Text :
https://doi.org/10.1172/JCI89401