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作 者:胡艳红[1] 黄秀榕[2] 祁明信[1] 侯补元[2]
机构地区:[1]福建中医药大学附属第二人民医院,福建福州350003 [2]福建中医药大学病理生理研究中心,福建福州350003
出 处:《福建中医药大学学报》2011年第4期16-18,共3页Journal of Fujian College of Traditional Chinese Medicine
基 金:福建省科技厅青年人才基金项目(2008F3050)
摘 要:目的探讨中药单体榄香烯(Ele)对人晶状体上皮细胞系(HLE-B3)内蛋白激酶A(PKA)及mRNA表达的影响。方法利用碱性成纤维细胞生长因子(rhbFGF)诱导HLE-B3增殖,将80mg/L的Ele作用在处于增殖状态下的HLE-B3 24 h,流式细胞术检测HLE-B3内PKA的表达,RT-PCR法检测HLE-B3内PKA mRNA表达。结果 rhbFGF组HLE-B3内PKA表达(33.250±2.242)较空白组(46.847±1.673)明显下降(P<0.01),Ele组(64.110±2.933)较rhbFGF组明显升高(P<0.01)。rhbFGF组HLE-B3内PKA mRNA表达(0.734±0.041)较空白组(0.927±0.040)明显下降(P<0.01),Ele组(1.196±0.066)较rhbFGF组明显升高(P<0.01)。结论上调HLE-B3内PKA表达、激活细胞内PKA信号转导途径可能是Ele抑制HLE-B3增殖的作用机制。Objective To investigate the effect of elemene(Ele) on expression levels of protein kinase A(PKA) and its mRNA in human lens epithelial cells B3(HLE-B3).Methods The proliferation of HLE-B3 was induced by 10 ng/mL recombinant human basic fibroblast growth factor(rhbFGF),then proliferative HLE-B3 were incubated with 80 mg/L Ele in CO2 incubator for 24 hours.The expression levels of PKA and its mRNA in HLE-B3 were detected by flow cytometry,RT-PCR respectively.Results Compared with control group,the expression level of PKA,PKA mRNA in HLE-B3 in rhbFGF group was decreased respectively(P0.01).Compared with rhbFGF group,the expression level of PKA,PKA mRNA in HLE-B3 in Ele group was increased respectively(P0.01).Conclusion Ele could up-regulate PKA and its mRNA expressions and activate PKA signal transduction pathway in HLE-B3,which was probably the mechanism of proliferative inhibition of HLE-B3 by Ele.
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