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首页> 外文期刊>Phytotherapy research: PTR >Sambucus Williamsii Hance Promotes MC3T3-E1 Cells Proliferation and Differentiation via BMP-2/Smad/p38/JNK/Runx2 Signaling Pathway
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Sambucus Williamsii Hance Promotes MC3T3-E1 Cells Proliferation and Differentiation via BMP-2/Smad/p38/JNK/Runx2 Signaling Pathway

机译:Sambucus Williamsii Hance通过BMP-2 / Smad / p38 / JNK / Runx2信号通路促进MC3T3-E1细胞的增殖和分化

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The 50% ethanol elution fractions of root-bark of Sambucus Williamsii Hance (rbSWH) evaluated the effect of proliferation and differentiation on preosteoblast MC3T3-E1 cell, and the mechanism of actions. We found that rbSWH(30, 60, and 90 mu g/mL) can enhance cell proliferation by MTT assay and promote alkaline phosphatase (ALP) and bone Gla protein (BGP) activities, type I collagen (Col-I) synthesis, and mineralization nodule formation in primary cultured osteoblasts. The results showed that rbSWH can increase mRNA levels of BMP-2 and Runx2 using real-time reverse transcription-quantitative polymerase chain reaction, whereas the BMP-2 antagonist Noggin attenuated the increase of ALP activity induced by rbSWH, indicating that BMP-2 expression was required for the action of rbSWH in osteoblastic. We also found that rbSWH can enhance the expressions of BMP-2, BMPRIB, BMPRII, phosphorylation of Smad, JNK and p38, and Runx2 proteins by western blotting. In addition, pretreatment of cells with p38 inhibitor (SB203580) or JNK inhibitor (SP600125) can antagonize the elevation of BMP-2 expression, ALP activity, and cell viability induced by rbSWH. Taken together, our results provided an evidence that rbSWH can promote MC3T3-E1 cell proliferation and differentiation via BMP-2/Smad/p38/JNK/Runx2 signaling pathway. Copyright (C) 2015 John Wiley & Sons, Ltd.
机译:接骨木(Sambucus Williamsii Hance)(rbSWH)根皮的50%乙醇洗脱级分评估了增殖和分化对成骨细胞MC3T3-E1细胞的影响及其作用机理。我们发现rbSWH(30、60和90μg / mL)可以通过MTT分析增强细胞增殖并促进碱性磷酸酶(ALP)和骨Gla蛋白(BGP)活性,I型胶原(Col-I)合成以及原代培养成骨细胞中的矿化结节形成。结果表明,rbSWH可通过实时逆转录定量聚合酶链反应提高BMP-2和Runx2的mRNA水平,而BMP-2拮抗剂Noggin减弱了rbSWH诱导的ALP活性的增加,表明BMP-2表达rbSWH在成骨细胞中的作用是必需的。我们还发现rbSWH可以通过Western blotting增强BMP-2,BMPRIB,BMPRII的表达,Smad,JNK和p38的磷酸化以及Runx2蛋白的表达。此外,用p38抑制剂(SB203580)或JNK抑制剂(SP600125)预处理细胞可以拮抗rbSWH诱导的BMP-2表达,ALP活性和细胞活力。两者合计,我们的结果提供了证据,rbSWH可以通过BMP-2 / Smad / p38 / JNK / Runx2信号通路促进MC3T3-E1细胞增殖和分化。版权所有(C)2015 John Wiley&Sons,Ltd.

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