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Increased OPG/RANKL ratio in the conditioned medium of soybean-treated osteoblasts suppresses RANKL-induced osteoclast differentiation

机译:在大豆处理过的成骨细胞的条件培养基中增加的OPG / RANKL比可抑制RANKL诱导的破骨细胞分化

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Soybean is a major dietary source of isoflavones, particularly daidzein and genistein, which stimulate osteoblastic functions that are initiated by binding to estrogen receptor (ER)-α and ER-β found on osteoblasts. However, coupled with a low expression of ER-α and ER-β in osteoclasts, the inhibitory effects of soy isoflavones on osteoclast differentiation is likely mediated through paracrine factors produced by osteoblasts. Therefore, in this study, we investigated whether soybean can indirectly inhibit osteoclast differentiation through the modulation of osteoclastic factors produced by osteoblasts. Treatment with soybean extracts increased the levels of osteoprotegerin (OPG) and decreased those of receptor activator of nuclear factor-κB ligand (RANKL) in the conditioned medium?(CM) of MC3T3-E1 osteoblasts. Subsequently, the RANKL-induced RAW264.7 osteoclast formation was markedly inhibited by treatment with CM collected from MC3T3-E1 osteoblasts incubated with soybean extracts (S-CM). Similarly, S-CM significantly attenuated the RANKL-induced increase in the mRNA and protein levels of matrix metalloproteinase-9 (MMP-9), a potential biomarker gene of osteoclast differentiation, through the suppression of nuclear factor of activated T?cells?c1 (NFATc1) activation. Of note, a soybean concentration of 0.001?mg/ml further increased the OPG/RANKL ratio compared to treatment with a 0.1?mg/ml soybean concentration and was overall, more effective at inhibiting RANKL-induced osteoclast formation and MMP-9 expression. Taken together, our data demonstrate that treatment with soybean extracts stimulates the secretion of OPG and inhibits that of RANKL, thus inhibiting RANKL-induced osteoclast differentiation through the suppression of NFATc1 activation.
机译:大豆是异黄酮的主要饮食来源,尤其是大豆黄酮和染料木黄酮,它们通过与成骨细胞上发现的雌激素受体(ER)-α和ER-β结合而刺激成骨细胞功能。然而,再加上破骨细胞中ER-α和ER-β的低表达,大豆异黄酮对破骨细胞分化的抑制作用可能是由成骨细胞产生的旁分泌因子介导的。因此,在这项研究中,我们调查了大豆是否可以通过调节成骨细胞产生的破骨细胞因子来间接抑制破骨细胞分化。在MC3T3-E1成骨细胞的条件培养基(CM)中,大豆提取物处理可增加骨保护素(OPG)的水平,并降低核因子-κB配体(RANKL)的受体激活剂的水平。随后,通过用与大豆提取物(S-CM)孵育的MC3T3-E1成骨细胞收集的CM处理,可明显抑制RANKL诱导的RAW264.7破骨细胞形成。同样,S-CM通过抑制活化的T细胞的核因子c1,显着减弱了RANKL诱导的基质金属蛋白酶9(MMP-9)的mRNA和蛋白质水平的增加,基质金属蛋白酶9是破骨细胞分化的潜在生物标记基因。 (NFATc1)激活。值得注意的是,与以0.1?mg / ml的大豆处理相比,0.001?mg / ml的大豆进一步提高了OPG / RANKL的比值,并且总体而言,在抑制RANKL诱导的破骨细胞形成和MMP-9表达方面更为有效。两者合计,我们的数据表明用大豆提取物处理刺激OPG的分泌并抑制RANKL的分泌,从而通过抑制NFATc1活化来抑制RANKL诱导的破骨细胞分化。

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