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雌二醇对大鼠成肌细胞中 Fhl1 的转录调控。

Transcriptional regulation of Fhl1 by estradiol in rat myoblastocytes.

机构信息

Department of Pediatric Surgery, Shengjing Hospital, China Medical University, Shenyang 110004, China.

出版信息

Steroids. 2010 Apr;75(4-5):368-72. doi: 10.1016/j.steroids.2010.01.021. Epub 2010 Feb 10.

Abstract

Fhl1 (Four and a Half LIM domain 1) regulates muscle growth and development. In addition, skeletal myoblast growth is significantly affected by gender differences, implicating estrogen in the regulation of muscle development. We sought to determine if estrogen influences Fhl1 gene expression levels in rat L6GNR4 myoblastocytes that express the estrogen receptor beta (ERbeta), while luciferase assay, electrophoretic mobility shift assay (EMSA), and chromatin immunoprecipitation (ChIP) assay were employed to confirm the interaction between ERbeta and Fhl1. Treatment of L6GNR4 cells with physiological levels of 17beta-estradiol (E2) results in markedly decreased endogenous Fhl1 expression. Tamoxifen, an ER antagonist, partially reverses E2-mediated Fhl1 down-regulation in L6GNR4 cells. Furthermore, luciferase assay and EMSA identified a novel promoter region of Fhl1 that directly interacts with ERbeta. ChIP of the ERbeta-Fhl1 promoter complex from L6GNR4 cells confirmed that endogenous ERbeta interacts with this region. These data indicate that E2 down-regulates Fhl1 expression through its binding to the ERbeta. This is the first report of a small molecule that can affect Fhl1 expression. E2 may therefore be useful in developing new strategies for regulating Fhl1 expression and understanding the influence of estrogen on muscle growth and development.

摘要

Fhl1(Four and a Half LIM domain 1)调节肌肉生长和发育。此外,骨骼肌成肌细胞的生长受到性别差异的显著影响,这暗示着雌激素在肌肉发育的调节中起作用。我们试图确定雌激素是否会影响表达雌激素受体β(ERβ)的大鼠 L6GNR4 成肌细胞中的 Fhl1 基因表达水平,同时利用荧光素酶检测、电泳迁移率变动分析(EMSA)和染色质免疫沉淀(ChIP)实验来证实 ERβ与 Fhl1 之间的相互作用。用生理浓度的 17β-雌二醇(E2)处理 L6GNR4 细胞,会导致内源性 Fhl1 表达明显下降。他莫昔芬是一种 ER 拮抗剂,可部分逆转 E2 介导的 L6GNR4 细胞中 Fhl1 的下调。此外,荧光素酶检测和 EMSA 鉴定了 Fhl1 的一个新的启动子区域,该区域与 ERβ直接相互作用。从 L6GNR4 细胞的 ERβ-Fhl1 启动子复合物的 ChIP 实验证实了内源性 ERβ与该区域相互作用。这些数据表明,E2 通过与 ERβ 结合来下调 Fhl1 的表达。这是第一个报道小分子可以影响 Fhl1 表达的报告。因此,E2 可能有助于开发调节 Fhl1 表达的新策略,并深入了解雌激素对肌肉生长和发育的影响。

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