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作 者:王佳媚[1] 杨桂兰[2] 赵敏[2] 王剑峰[2] 潘之[2] 肖辉[2]
机构地区:[1]兰州大学第二临床医学院,兰州730000 [2]兰州军区兰州总医院皮肤科,甘肃省干细胞与基因药物重点实验室
出 处:《实用皮肤病学杂志》2013年第6期331-334,共4页Journal of Practical Dermatology
基 金:中华医学会皮肤性病学分会-朗生医药皮肤病学研究基金
摘 要:目的探讨白芍总苷(TGP)对人永生化角质形成细胞(HaCaT细胞)增生及分泌细胞间黏附分子(ICAM)-1的影响,探讨可能涉及的信号传导通路。方法用500 U/ml干扰素(IFN)-γ诱导HaCaT细胞,不同浓度TGP(0.5~312.5μg/ml)作用于HaCaT细胞。四甲基偶氮唑盐(MTT)法观察TGP对HaCaT细胞增生活性的影响。酶联免疫吸附试验(ELISA)及荧光免疫组化法检测HaCaT细胞表达ICAM-1的水平。结果 TGP在低浓度(0.5~25.0μg/ml)时对HaCaT细胞增生活性有促进作用,在高浓度(62.5~125.0μg/ml)时对HaCaT细胞增生活性呈抑制作用。0.5~25.0μg/ml TGP可显著降低HaCaT细胞表达ICAM-1的水平(P<0.05,P<0.01)。结论 TGP对IFN-γ上调HaCaT细胞分泌ICAM-1有显著的抑制作用,可能是TGP抗炎作用机制之一。Objective To evaluate the effects of total glucosides of paeony (TGP) on cell proliferation of human HaCaT keratinocytes and the expression of ICAM-1, and explore the signaling pathways which may be involved in the process. Methods HaCaT cells were stimulated by 500 U/mL IFN-γ, then incubated with TGP of various concentrations (0.5 to 312.5 μg/ml). MTT assay was performed to detect the cell proliferation of HaCaT cells. The expression of ICAM-1 in HaCaT cells was evaluated by enzyme linked immunosorbent assay (ELISA) and lfuorescent immunohistochemical technology. Results The proliferation of HaCaT cells was promoted by TGP of low concentrations (0.5 to 25.0μg/ml), but inhibited by TGP of high concentration (62.5 to 125.0μg/ml). TGP of low concentrations (0.5 to 25.0μg/mL) signiifcantly reduced the expression of ICAM-1. Conclusion TGP signiifcantly inhibited the upregulated ICAM-1 secretion of HaCaT cells which induced by IFN-γ, that may be one of the anti-inlfammatory mechanism of TGP.
关 键 词:白芍总苷 人永生化角质形成细胞 细胞间黏附分子-1 Γ干扰素
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