Takagi Tomohiro, Inoue Hirofumi, Takahashi Nobuyuki, Katsumata-Tsuboi Rie, Uehara Mariko
Department of Nutritional Science and Food Safety, Faculty of Applied Bioscience, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo 156-8502, Japan.
Department of Nutritional Science and Food Safety, Faculty of Applied Bioscience, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo 156-8502, Japan.
Biochem Biophys Res Commun. 2017 Jan 29;483(1):718-724. doi: 10.1016/j.bbrc.2016.12.075. Epub 2016 Dec 12.
Sulforaphane (SFN), a kind of isothiocyanate, is derived from broccoli sprouts. It has anti-tumor, anti-inflammatory, and anti-oxidation activity. The molecular function of SFN in the inhibition of osteoclast differentiation is not well-documented. In this study, we assessed the effect of SFN on osteoclast differentiation in vitro. SFN inhibited osteoclast differentiation in both bone marrow cells and RAW264.7 cells. Key molecules involved in the inhibitory effects of SFN on osteoclast differentiation were determined using a microarray analysis, which showed that SFN inhibits osteoclast-associated genes, such as osteoclast-associated receptor (OSCAR), nuclear factor of activated T cells cytoplasmic-1, tartrate-resistant acid phosphatase, and cathepsin K. Moreover, the mRNA expression levels of the cell-cell fusion molecules dendritic cell specific transmembrane protein (DC-STAMP) and osteoclast stimulatory transmembrane protein (OC-STAMP) were strongly suppressed in cells treated with SFN. Furthermore, SFN increased the phosphorylation of signal transducer and activator of transcription 1 (STAT1), a regulator of macrophage and osteoclast cell fusion. Thus, our data suggested that SFN significantly inhibits the cell-cell fusion molecules DC-STAMP and OC-STAMP by inducing the phosphorylation of STAT1 (Tyr701), which might be regulated by interactions with OSCAR.
萝卜硫素(SFN)是一种异硫氰酸盐,源自西兰花芽。它具有抗肿瘤、抗炎和抗氧化活性。SFN在抑制破骨细胞分化中的分子功能尚未得到充分记载。在本研究中,我们评估了SFN在体外对破骨细胞分化的影响。SFN抑制骨髓细胞和RAW264.7细胞中的破骨细胞分化。使用微阵列分析确定了参与SFN对破骨细胞分化抑制作用的关键分子,结果表明SFN抑制破骨细胞相关基因,如破骨细胞相关受体(OSCAR)、活化T细胞核因子胞质1、抗酒石酸酸性磷酸酶和组织蛋白酶K。此外,在用SFN处理的细胞中,细胞间融合分子树突状细胞特异性跨膜蛋白(DC-STAMP)和破骨细胞刺激跨膜蛋白(OC-STAMP)的mRNA表达水平受到强烈抑制。此外,SFN增加了信号转导和转录激活因子1(STAT1)的磷酸化,STAT1是巨噬细胞和破骨细胞融合的调节因子。因此,我们的数据表明,SFN通过诱导STAT1(Tyr701)的磷酸化显著抑制细胞间融合分子DC-STAMP和OC-STAMP,这可能受与OSCAR相互作用的调节。