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雌激素通过拮抗DUX4活性增强面肩肱型肌营养不良症中的成肌细胞分化。

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

作者信息

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

出版信息

J Clin Invest. 2017 Apr 3;127(4):1531-1545. doi: 10.1172/JCI89401. Epub 2017 Mar 6.

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 β (ERβ), 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. ERβ 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.

摘要

面肩肱型肌营养不良症(FSHD)是一种常染色体显性神经肌肉疾病,其症状具有极大变异性,女性受影响程度低于男性,且无症状携带者比例更高。该疾病涉及的性别相关因素尚不清楚。在此,我们利用从FSHD患者分离出的成肌细胞(FSHD成肌细胞)来研究雌激素对肌肉特性的影响。我们的结果表明,雌激素可抵消FSHD成肌细胞的分化障碍,而不影响细胞增殖或存活。雌激素作用由雌激素受体β(ERβ)介导,ERβ可降低双同源盒4(DUX4)的染色质占有率和转录活性,DUX4蛋白的异常表达与FSHD发病机制有关。在成肌细胞分化过程中,我们观察到DUX4的水平和活性逐渐增加,并与其在细胞核中的募集增强有关。ERβ通过将DUX4重新定位到细胞质中来干扰这种募集。这项研究确定雌激素是一种潜在的疾病修饰因子,通过防止该疾病中的成肌细胞分化障碍,成为FSHD中性别相关差异的基础。

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