Erratum: Estradiol Modulates the Expression Pattern of Myosin Heavy Chain Subtypes via an ERα-Mediated Pathway in Muscle-Derived Tissues and Satellite Cells
2017-07-25T13:47:50Z (GMT) by
<b><i>Background: </i></b>Muscle-derived satellite cells (MDSCs) express MHC molecules intimately related to muscle function, which is supposed to be affected by local estrogen (E<sub>2</sub>) levels. However, cellular targets and molecular mechanisms involved are poorly understood. <b><i>Methods: </i></b>Genioglossus (GG) muscle tissues and MDSCs were derived from SHAM, ovariectomized or ovariectomized and 17 β-estradiol injected rats (n=10 ⁄ group). ERα, ERβ, MHC expression and underlying regulatory mechanisms were investigated by RT-PCR, western blot and immunohistochemistry, inter alia upon selective antagonist exposure and Si-RNA transfection. MDSC viability and cell cycle were examined by MTT and flow cytometry. <b><i>Results: </i></b>E<sub>2</sub> upregulated MHC-I and downregulated MHC-IIb expression in MDSCs. E<sub>2</sub> mediated effects on these molecules were inhibited by ERα-selective antagonist MPP and si-ERα, whereas they persisted upon exposure to ERβ-selective antagonist PHTPP. ERα was significantly higher expressed in muscle tissues compared to ERβ. ER positive stainings were fewer in the ovariectomized than in the SHAM group. Injection of E<sub>2</sub> only increased the positive staining of ERα, but not of ERβ. <b><i>Conclusion: </i></b>Results suggest that E<sub>2</sub> regulates MHC expression mainly through an ERα-mediated pathway with opposing effects on MHC-I and MHC-IIb. Thus, different hormonal processes that impact muscular pathophysiology presumably govern the functional properties of these molecules.