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作 者:行敏[1] 耿龙[1] 任宏伟[1] 屈慧明[1] 王雪[1] 季永智[1] 魏仲香[1] 周鸿波[1]
机构地区:[1]中国医科大学附属第一医院皮肤性病科,沈阳110001
出 处:《中华微生物学和免疫学杂志》2011年第8期685-688,共4页Chinese Journal of Microbiology and Immunology
基 金:国家自然科学基金(30872277);教育部长江学者和创新团队发展计划项目(IRT0760);辽宁省教育厅创新团队项目(2008T197)
摘 要:目的观察白细胞介素-17(IL-17)对HaCaT细胞分泌血管内皮生长因子(VEGF)的影响及紫草素的干预作用。方法收集IL-17刺激组和紫草素处理后HaCaT细胞及其培养上清,分别用双抗体夹心酶联免疫吸附法(ELISA)及实时荧光免疫定量-聚合酶链反应法(RT-PCR)检测VEGF含量。应用细胞计数盒-8(CCK-8)检测各组HaCaT细胞活力。结果与对照组相比,不同时间IL-17刺激组HaCaT细胞及其培养上清中VEGF表达均高于对照组(P〈0.001);紫草素处理组HaCaT细胞及其培养上清VEGF表达均低于IL-17处理组(P〈0.001);与对照组比较,CCK-8检测各组HaCaT细胞活力无明显差异(P〉0.05)。结论IL-17可促进HaCaT细胞分泌VEGF,呈时间依赖型,而紫草素对其具有抑制作用。Objective To investigate whether IL-17 could stimulate the vascular endothelial growth factor (VEGF) production on HaCaT cells alone. We also investigated whether shikonin could inhibi- ted the proinflarnation effects of interleukin-17 (IL-17) acting on HaCaT cells. Methods We examined the expression of VEGF by double antibody sandwich enzyme-linked immunosorbent assay (ELISA) and real- time polymerase chain reaction(RT-PCR) in HaCaT cells and the cell supernatant. The viability of HaCaT cells in the drug group was detected by the Cell Counting Kit-8 ( CCK-8 ). Results The expression of VEGF in different time IL-17-stimulated groups on HaCaT cells and the cell supernatant were higher than the con- trol group(P〈0.001 ). The expression of VEGF in different drug treatment groups on HaCaT cells and the cell supernatant were lower than the stimulated group by IL-17 ( P〈0. 001 ). The cell viability of different drug treatment groups have no significant difference(P〉0.05). Conclusion We show that IL-17 specific- ally and time-dependently augmented and induced VEGF expression on HaCaT cells and the cell supernatant Then shikonin markedly inhibited the increase tengency of IL-17 effection on HaCaT cells and the cell supernatant level.
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