Veterans Administration Medical Center and Division of Endocrinology, Metabolism, and Lipids, Department of Medicine, Emory University School of Medicine, Atlanta, GA, USA.
J Bone Miner Res. 2011 Oct;26(10):2537-47. doi: 10.1002/jbmr.456.
The heterogeneous nuclear ribonucleoprotein (hnRNP)-like estrogen response element-binding protein (ERE-BP) competes with estrogen receptor α (ERα) for occupancy of estrogen response elements (EREs). Here we report that ERE-BP potently stimulates osteoclastogenesis. ERE-BP mRNA and protein were found to be expressed ubiquitously in bone. Overexpression of ERE-BP in cultured osteoblasts stimulated expression of the receptor activator of NF-κB ligand (RANKL) and decreased osteoprotegerin (OPG). The effect of ERE-BP on RANKL was shown to be transcriptional in transient transfection assay and competed with via the ER. Constitutive expression of ERE-BP increased the sensitivity of cells toward 1,25-dihydroxyvitamin D(3) stimulation of RANKL expression. In contrast, knockdown of ERE-BP in stromal ST-2 cells decreased basal RANKL promoter activity. Cocultures of ERE-BP lentivirus-transduced ST-2 cells with spleen monocytes induced formation of multinucleated osteoclasts (OCs) characterized by tartrate-resistant acid phosphatase, calcitonin receptors, and functional calcium resorption from bone slices. Although ERα competed with ERE-BP for an ERE in a dose-dependent manner, ERE-BP was an independent and potent regulator of RANKL and osteoclastogenesis. In preosteoclastic RAW cells, overexpression of ERE-BP increased RANK, upregulated NF-κB signaling, and enhanced differentiation toward a mature OC phenotype independent of RANKL. These results identify ERE-BP as a potent modulator of osteoclastogenesis. We hypothesize that ERE-BP may play a critical role in the regulation of bone homeostasis as a modulator of estrogen sensitivity as well as by direct action on the transcription of critical osteoclastogenic genes.
异质核核糖核蛋白 (hnRNP)-样雌激素反应元件结合蛋白 (ERE-BP) 与雌激素受体 α (ERα) 竞争雌激素反应元件 (ERE) 的结合。在这里,我们报告 ERE-BP 可强力刺激破骨细胞生成。发现 ERE-BP mRNA 和蛋白在骨中广泛表达。在培养的成骨细胞中过表达 ERE-BP 可刺激核因子-κB 受体激活剂配体 (RANKL) 的表达并降低骨保护素 (OPG)。瞬时转染测定显示,ERE-BP 对 RANKL 的作用是转录性的,并通过 ER 竞争。ERE-BP 的组成型表达增加了细胞对 1,25-二羟基维生素 D(3)刺激 RANKL 表达的敏感性。相反,基质 ST-2 细胞中 ERE-BP 的敲低降低了基础 RANKL 启动子活性。将 ERE-BP 慢病毒转导的 ST-2 细胞与脾单核细胞共培养可诱导形成多核破骨细胞 (OC),其特征为抗酒石酸酸性磷酸酶、降钙素受体和从骨切片中进行功能钙吸收。尽管 ERα 以剂量依赖的方式与 ERE-BP 竞争 ERE,但 ERE-BP 是 RANKL 和破骨细胞生成的独立且强力的调节剂。在预破骨细胞 RAW 细胞中,过表达 ERE-BP 可增加 RANK,上调 NF-κB 信号,并增强向成熟 OC 表型的分化,而无需 RANKL。这些结果表明 ERE-BP 是破骨细胞生成的有力调节剂。我们假设 ERE-BP 可能作为雌激素敏感性的调节剂以及通过对关键破骨细胞生成基因的转录直接作用,在骨稳态的调节中发挥关键作用。