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山奈酚可刺激骨涎蛋白基因转录和新骨形成。

Kaempferol stimulates bone sialoprotein gene transcription and new bone formation.

机构信息

Department of Periodontology, Nihon University School of Dentistry at Matsudo, Chiba 271-8587, Japan.

出版信息

J Cell Biochem. 2010 Aug 15;110(6):1342-55. doi: 10.1002/jcb.22649.

DOI:10.1002/jcb.22649
PMID:20564228
Abstract

Kaempferol is a typical flavonol-type flavonoid that is present in a variety of vegetables and fruits, and has a protective effect on postmenopausal bone loss. Bone sialoprotein (BSP) is thought to function in the initial mineralization of bone and could be crucial for osteoblast differentiation, bone matrix mineralization and tumor metastasis. In the present study we investigated the regulation of BSP transcription by kaempferol in rat osteoblast-like UMR106 cells, and the effect of kaempferol on new bone formation. Kaempferol (5 microM) increased BSP and Osterix mRNA levels at 12 h and up-regulated Runx2 mRNA expression at 6 h. Kaempferol increased luciferase activity of the construct pLUC3, which including the promoter sequence between nucleotides -116 to +60. Transcriptional stimulation by kaempferol abrogated in constructs included 2 bp mutations in the inverted CCAAT, CRE, and FRE elements. Gel shift analyses showed that kaempferol increased nuclear protein binding to CRE and FRE elements, whereas the CCAAT-protein complex did not change after kaempferol stimulation. Twelve daily injections of 5 microM kaempferol directly into the periosteum of parietal bones of newborn rats increased new bone formation. These data suggest that kaempferol increased BSP gene transcription mediated through inverted CCAAT, CRE, and FRE elements in the rat BSP gene promoter, and could induce osteoblast activities in the early stage of bone formation.

摘要

山奈酚是一种典型的黄酮醇型类黄酮,存在于各种蔬菜和水果中,对绝经后骨质流失具有保护作用。骨唾液蛋白(BSP)被认为在骨的初始矿化中起作用,并且对成骨细胞分化、骨基质矿化和肿瘤转移可能至关重要。在本研究中,我们研究了山奈酚对大鼠成骨样 UMR106 细胞中 BSP 转录的调节作用,以及山奈酚对新骨形成的影响。山奈酚(5μM)在 12 小时时增加 BSP 和 Osterix mRNA 水平,并在 6 小时时上调 Runx2 mRNA 表达。山奈酚增加了包含核苷酸 -116 到 +60 之间启动子序列的构建体 pLUC3 的荧光素酶活性。山奈酚对包括在倒置 CCAAT、CRE 和 FRE 元件中 2 个碱基突变的构建体的转录刺激被消除。凝胶移位分析表明,山奈酚增加了核蛋白与 CRE 和 FRE 元件的结合,而 CCAAT-蛋白复合物在山奈酚刺激后没有改变。12 天每天向新生大鼠顶骨骨膜内直接注射 5μM 山奈酚可增加新骨形成。这些数据表明,山奈酚通过大鼠 BSP 基因启动子中的倒置 CCAAT、CRE 和 FRE 元件增加了 BSP 基因的转录,并且可以在骨形成的早期诱导成骨细胞的活性。

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