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首页> 外文期刊>International journal of molecular medicine >The estrogen 17beta-estradiol and phytoestrogen genistein mediate differential effects on osteoblastic NF-kappaB activity.
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The estrogen 17beta-estradiol and phytoestrogen genistein mediate differential effects on osteoblastic NF-kappaB activity.

机译:雌激素17β-雌二醇和植物雌激素染料木黄酮介导对成骨细胞NF-κB活性的不同影响。

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摘要

Estrogen (17beta-estradiol) and genistein, a phytoestrogen, are both endowed with anabolic activities on bone in vivo and stimulate osteoblastic differentiation and mineralization in vitro. However, the mechanisms by which these agents promote osteoblastic differentiation and bone anabolic responses are multifactorial and only partly understood. Recently, the NF-kappaB signal transduction pathway was implicated as a negative regulator of osteoblastic differentiation and suppression of this pathway leads to osteoblastic differentiation and mineralization in vitro. To examine whether estrogen and/or genistein regulate osteoblast differentiation by modulating the NF-kappaB pathway, we examined the effect of 17beta-estradiol and genistein on basal and TNFalpha-stimulated NF-kappaB activity in the preosteoblastic cell line MC3T3. MC3T3 cells were transiently transfected with an NF-kappaB responsive luciferase reporter and cultured for 24 h with either vehicle, or physiological doses of 17beta-estradiol (10(-9) to 10(-7) M), or genistein (10(-6) to 10(-5) M). Our data reveal that while 17beta-estradiol had no effect on basal NF-kappaB activity in MC3T3 cells, it significantly antagonized NF-kappaB activity induced by TNFalpha (1 or 10 ng/ml). By contrast, genistein (10(-6) or 10(-5) M) significantly increased NF-kappaB activity, and showed no antagonistic effects on TNFalpha-induced NF-kappaB promoter activity. These studies suggest that the estrogenic compounds, 17beta-estradiol and genistein, mediate very different actions on osteoblastic cells. While 17beta-estradiol may stimulate bone anabolism, in part, by antagonizing TNFalpha-induced NF-kappaB activation, genistein not only fails to prevent cytokine-induced NF-kappaB activation, but directly promotes NF-kappaB activation in MC3T3 cells. These data suggest important mechanistic differences in the mechanisms by which 17beta-estradiol and genistein promote osteoblast differentiation.
机译:雌激素(17β-雌二醇)和染料木黄酮(一种植物雌激素)在体内都具有对骨骼的合成代谢活性,并在体外刺激成骨细胞的分化和矿化。然而,这些试剂促进成骨细胞分化和骨合成代谢反应的机制是多因素的,并且仅是部分理解的。最近,NF-kappaB信号转导途径被认为是成骨细胞分化的负调节剂,并且该途径的抑制导致体外成骨细胞的分化和矿化。为了检查雌激素和/或染料木黄酮是否通过调节NF-kappaB通路来调节成骨细胞分化,我们检查了17β-雌二醇和染料木黄酮对成骨前细胞细胞系MC3T3中基础和TNFα刺激的NF-κB活性的影响。 MC3T3细胞用NF-κB响应荧光素酶报道基因瞬时转染,并与媒介物或生理剂量的17β-雌二醇(10(-9)至10(-7)M)或染料木黄酮(10(- 6)至10(-5)M)。我们的数据显示,尽管17β-雌二醇对MC3T3细胞中的基础NF-kappaB活性没有影响,但它显着拮抗TNFalpha(1或10 ng / ml)诱导的NF-kappaB活性。相反,金雀异黄素(10(-6)或10(-5)M)显着增加了NF-kappaB的活性,并且对TNFalpha诱导的NF-kappaB启动子的活性没有拮抗作用。这些研究表明,雌激素化合物17β-雌二醇和染料木黄酮对成骨细胞的介导作用非常不同。尽管17β-雌二醇可能通过拮抗TNFα诱导的NF-kappaB激活而部分刺激骨合成代谢,但染料木黄酮不仅不能阻止细胞因子诱导的NF-kappaB激活,而且可以直接促进MC3T3细胞中NF-kappaB的激活。这些数据表明17β-雌二醇和染料木黄酮促进成骨细胞分化的机制上存在重要的机械差异。

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