CAJ | 학술논문

目的：考察松果菊苷对大鼠成骨细胞增殖的影响及作用机制。方法将不同浓度的松果菊苷（0.01，0.1，1.0，10.0，100 nmol/L）及MAPK/ERK信号通路抑制剂PD98059（20μmol/L）与成骨细胞共培养12，24，36，48，60 h后，采用MTT法检测细胞增殖情况。酶联免疫吸附法（ELISA）和qRT-PCR法检测细胞上清中和成骨细胞中骨钙素（BGP）和骨形态发生蛋白（BMP-2）的表达水平。Western blotting检测成骨细胞中Smad4、ERK1/2和p-ERK1/2的蛋白表达水平。结果松果菊苷能够促进大鼠成骨细胞的增殖，而且能诱导ERK 的磷酸化从而激活 MAPK/ERK 信号通路，并提高成骨细胞中 BMP-2和 Smad4的表达而激活BMP/Smad信号通路。加入PD98059后，松果菊苷诱导的BMP-2和Smad4表达及成骨细胞增殖均受到抑制。结论松果菊苷可通过激活ERK/BMP-2信号通路促进大鼠的成骨细胞增殖。
목적：고찰송과국감대대서성골세포증식적영향급작용궤제。방법장불동농도적송과국감（0.01，0.1，1.0，10.0，100 nmol/L）급MAPK/ERK신호통로억제제PD98059（20μmol/L）여성골세포공배양12，24，36，48，60 h후，채용MTT법검측세포증식정황。매련면역흡부법（ELISA）화qRT-PCR법검측세포상청중화성골세포중골개소（BGP）화골형태발생단백（BMP-2）적표체수평。Western blotting검측성골세포중Smad4、ERK1/2화p-ERK1/2적단백표체수평。결과송과국감능구촉진대서성골세포적증식，이차능유도ERK 적린산화종이격활 MAPK/ERK 신호통로，병제고성골세포중 BMP-2화 Smad4적표체이격활BMP/Smad신호통로。가입PD98059후，송과국감유도적BMP-2화Smad4표체급성골세포증식균수도억제。결론송과국감가통과격활ERK/BMP-2신호통로촉진대서적성골세포증식。
ObjectiveTo investigate the effect of echinacoside(ECH)on cell proliferation of rat osteoblast and its mechanism.MethodThe osteoblast was incubated with different concentration of ECH(0.01、0.1、1.0、10.0、100 nmol/L)or PD98059(20 μmol/L)which is an inhibitor of MAPK/ERK for 12、24、36、48 or 60 h. MTT method was used for the detection of cell proliferation. The protein and mRNA level of BGP and BMP-2 in supernatant and cells was measured by ELISA and qRT-PCR. Expression of smad4、ERK1/2 and p-ERK1/2 was detected by western blotting. ResultsThe cell proliferation of osteoblast was promoted by ECH. ECH induced expression of BMP-2 and smad4 to activate BMP/smad pathway,and also promoted the phosphorylation of ERK1/2 to activate MAPK/ERK pathway. While the activation of BMP/smad pathway was inhibited by PD98059.ConclusionsEchinacoside promotes cell proliferation of rat osteoblast through activating of ERK/BMP-2 signaling pathway.