Chen X W, Garner S C, Anderson J J B
Department of Nutrition, School of Public Health, University of North Carolina, Chapel Hill, NC 27599-7400, USA.
Biochem Biophys Res Commun. 2002 Jul 12;295(2):417-22. doi: 10.1016/s0006-291x(02)00667-8.
The hypothesis tested in this in vitro study was that the expression and production of dietary isoflavone-mediated osteoclastogenesis-regulatory cytokines, such as interleukin-6 (IL-6) and osteoprotegerin (OPG), are related to the different levels of estrogen receptors expressed in two hFOB osteoblastic cell lines. OPG mRNA expression was significantly increased in both hFOB1.19 and hFOB/ER9 cells treated with 17 beta-estradiol, genistein, or daidzein at 10(-8)M in comparison to vehicle (control) (P<0.05). In both cell lines, the release of IL-6 was suppressed, while OPG production was enhanced by isoflavone treatments (P<0.05). The increased expression of OPG and decreased IL-6 production by isoflavones were dose-dependent. Responses to isoflavones were much stronger in hFOB/ER9 cells, which express the estrogen receptor 20 times higher than those in hFOB1.19 cells. After adding the ER binding blocker, ICI-182,780, the effects of isoflavones on OPG and IL-6 production disappeared. In summary, the inhibition by dietary isoflavones of IL-6 production and the stimulation of OPG appear to be mediated, at least in part, via a genomic pathway operating through estrogen receptors and gene expression mechanisms.
本体外研究中所检验的假设是,膳食异黄酮介导的破骨细胞生成调节细胞因子(如白细胞介素-6(IL-6)和骨保护素(OPG))的表达和产生,与两种人永生化成骨细胞系(hFOB)中雌激素受体的不同表达水平相关。与载体(对照)相比,用10⁻⁸M的17β-雌二醇、染料木黄酮或大豆苷元处理的hFOB1.19和hFOB/ER9细胞中,OPG mRNA表达均显著增加(P<0.05)。在两种细胞系中,异黄酮处理均抑制了IL-6的释放,同时增强了OPG的产生(P<0.05)。异黄酮使OPG表达增加和IL-6产生减少呈剂量依赖性。hFOB/ER9细胞对异黄酮的反应要强得多,其雌激素受体表达量比hFOB1.19细胞高20倍。加入雌激素受体结合阻滞剂ICI-182,780后,异黄酮对OPG和IL-6产生的影响消失。总之,膳食异黄酮对IL-6产生的抑制作用和对OPG的刺激作用,似乎至少部分是通过雌激素受体和基因表达机制的基因组途径介导的。