Liu Chang-Geng, Luo Qi-Xian, Ling Tian-You, Mo Ye-Yue, Cheng Zi-Li, Huang Sheng-Gao, Mo Hui
Department of Stomatology, Guangfo Hospital, Guangzhou Medical University, Guangdong 528251, China.
Department of Stomatology, Second Xiangya Hospital, Central South University, Changsha 410011, China.
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2013 Dec;33(12):1658-64.
To study the effect of Erigeron Breviscapus (EB) at different concentrations and different intervention time points on the mRNA and protein expression of OPG/RANKL/RANK in MG63 osteoblast-like cells and RAW264. 7 pre-osteoclast cells cultured in vitro, thus exploring roles EB played in bone rebuilding and its mechanisms.
MG63 osteoblast-like cells and RAW264.7 pre-osteoclast cells were cultured in vitro. The 3rd passage cells were divided into the control group and different experimental groups. Total RNA and protein were respectively isolated from cells treated with different concentrations of EB (0, 0.001, 0.01, 0.1, and 1.0 mg/mL) for 48 h. Meanwhile, the protein was extracted from 0 and 1 mg/mL EB groups at 12, 24, and 48 h respectively. Expression of OPG mRNA and RANKL mRNA in MG63 osteoblast-like cells, and expression of RANK mRNA in RAW264.7 pre-osteoclast cells were detected by semi-quantitative RT-PCR. Expression of OPG protein and RANKL protein in MG63 osteoblast-like cells, and expression of RANK protein in RAW264. 7 pre-osteoclast cells were detected by Western blot.
Along with increased EB concentration, expression of OPG mRNA and protein in MG63 osteoblast-like cells was gradually lowered (P < 0.05) after 48-h intervention of EB, the expression of RANKL mRNA and protein in MG63 osteoblast-like gradually increased (P < 0.05); the expression of RANK mRNA in RAW264.7 pre-osteoclast cells increased (P < 0.05). But the expression of RANK mRNA was slightly lower in the 0.1 mg/mL EB group than in the 0.01 mg/mL EB group, and the expression of RANK protein in RAW264.7 pre-osteoclast cells gradually increased (P < 0.05). After treatment with 1 mg/mL EB for 12, 24, 48 h, the expression of OPG protein in MG63 osteoblast-like cells gradually decreased as time went by (P < 0.05), and the expression of RANKL protein in MG63 osteoblast-like and RANK protein in RAW264.7 pre-osteoclast cells gradually increased (P < 0.05). The expression of RANKL protein in RAW264.7 pre-osteoclast cells increased as time went by (P < 0.05).
EB could inhibit the expression of OPG in osteoblasts in a dose- and time-dependent manner, promote the expression of RANKL in osteoblasts and the secretion of RANK in pre-osteoclast, indicating EB might play roles in promoting bone resorption.
研究不同浓度、不同干预时间点灯盏花(EB)对体外培养的MG63成骨样细胞和RAW264.7前破骨细胞中OPG/RANKL/RANK的mRNA及蛋白表达的影响,从而探讨EB在骨重建中的作用及其机制。
体外培养MG63成骨样细胞和RAW264.7前破骨细胞。将第3代细胞分为对照组和不同实验组。分别提取用不同浓度EB(0、0.001、0.01、0.1和1.0mg/mL)处理48h的细胞的总RNA和蛋白。同时,分别在12、24和48h从0和1mg/mL EB组提取蛋白。采用半定量RT-PCR检测MG63成骨样细胞中OPG mRNA和RANKL mRNA的表达,以及RAW264.7前破骨细胞中RANK mRNA的表达。采用蛋白质印迹法检测MG63成骨样细胞中OPG蛋白和RANKL蛋白的表达,以及RAW264.7前破骨细胞中RANK蛋白的表达。
EB干预48h后,随着EB浓度升高,MG63成骨样细胞中OPG mRNA和蛋白表达逐渐降低(P<0.05),MG63成骨样细胞中RANKL mRNA和蛋白表达逐渐升高(P<0.05);RAW264.7前破骨细胞中RANK mRNA表达升高(P<0.05)。但0.1mg/mL EB组RANK mRNA表达略低于0.01mg/mL EB组,RAW264.7前破骨细胞中RANK蛋白表达逐渐升高(P<0.05)。用lmg/mL EB处理12、‘24、48h后,MG63成骨样细胞中OPG蛋白表达随时间逐渐降低(P<0.05),MG63成骨样细胞中RANKL蛋白及RAW264.7前破骨细胞中RANK蛋白表达逐渐升高(P<0.05)。RAW264.7前破骨细胞中RANKL蛋白表达随时间升高(P<0.05)。
EB可呈剂量和时间依赖性抑制成骨细胞中OPG的表达,促进成骨细胞中RANKL的表达及前破骨细胞中RANK的分泌,提示EB可能在促进骨吸收中发挥作用。