首页> 美国卫生研究院文献>BMB Reports >CCAAT/enhancer-binding protein beta (C/EBPβ) is an important mediator of 125 dihydroxyvitamin D3 (125D3)-induced receptor activator of nuclear factor kappa-B ligand (RANKL) expression in osteoblasts
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CCAAT/enhancer-binding protein beta (C/EBPβ) is an important mediator of 125 dihydroxyvitamin D3 (125D3)-induced receptor activator of nuclear factor kappa-B ligand (RANKL) expression in osteoblasts

机译:CCAAT /增强子结合蛋白β(C /EBPβ)是125二羟基维生素D3(125D3)诱导的成骨细胞核因子kappa-B配体(RANKL)表达受体激活剂的重要介体

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摘要

Receptor activator of nuclear factor kappa B ligand (RANKL) expression in osteoblasts is regulated by 1,25-dihydroxyvitamin D3 (1,25D3). CCAAT/enhancer-binding protein beta (C/EBPβ) has been proposed to function as a transcription factor and upregulate RANKL expression, but it is still uncertain how C/EBPβ is involved in 1,25D3-induced RANKL expression of osteoblasts. 1,25D3 stimulation increased the expression of RANKL and C/EPBβ genes in osteoblasts and enhanced phosphorylation and stability of these proteins. Moreover, induction of RANKL expression by 1,25D3 in osteoblasts was downregulated upon knockdown of C/EBPβ. In contrast, C/EBPβ overexpression directly upregulated RANKL promoter activity and exhibited a synergistic effect on 1,25D3-induced RANKL expression. In particular, 1,25D3 treatment of osteoblasts increased C/EBPβ protein binding to the RANKL promoter. In conclusion, C/EBPβ is required for induction of RANKL by 1,25D3.
机译:1,25-二羟基维生素D3(1,25D3)调节成骨细胞中核因子kappa B配体(RANKL)表达的受体激活剂。已经提出CCAAT /增强子结合蛋白β(C /EBPβ)起转录因子的作用并上调RANKL的表达,但仍不确定C /EBPβ如何参与1,25D3诱导的成骨细胞的RANKL表达。 1,25D3刺激增加了成骨细胞中RANKL和C /EPBβ基因的表达,并增强了这些蛋白质的磷酸化和稳定性。此外,在敲低C /EBPβ时,成骨细胞中1,25D3对RANKL表达的诱导被下调。相反,C /EBPβ的过表达直接上调了RANKL启动子的活性,并在1,25D3诱导的RANKL表达上表现出协同作用。特别地,1,25D3处理成骨细胞增加了C /EBPβ蛋白与RANKL启动子的结合。总之,C /EBPβ是1,25D3诱导RANKL所必需的。

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