中华微生物学和免疫学杂志
中華微生物學和免疫學雜誌
중화미생물학화면역학잡지
CHINESE JOURNAL OF MICROBIOLOGY AND IMMUNOLOGY
2011年
8期
685-688
,共4页
行敏%耿龙%任宏伟%屈慧明%王雪%季永智%魏仲香%周鸿波
行敏%耿龍%任宏偉%屈慧明%王雪%季永智%魏仲香%週鴻波
행민%경룡%임굉위%굴혜명%왕설%계영지%위중향%주홍파
银屑病%HaCaT细胞%IL-17%VEGF%紫草素
銀屑病%HaCaT細胞%IL-17%VEGF%紫草素
은설병%HaCaT세포%IL-17%VEGF%자초소
Psoriasis%HaCaT cell%IL-17%VEGF%Shikonin
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细胞及其培养土清,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。
目的 觀察白細胞介素-17(IL-17)對HaCaT細胞分泌血管內皮生長因子(VEGF)的影響及紫草素的榦預作用。方法 收集IL-17刺激組和紫草素處理後HaCaT細胞及其培養土清,分彆用雙抗體夾心酶聯免疫吸附法(ELISA)及實時熒光免疫定量-聚閤酶鏈反應法(RT-PCR)檢測VEGF含量。應用細胞計數盒-8(CCK-8)檢測各組HaCaT細胞活力。結果 與對照組相比,不同時間IL-17刺激組HaCaT細胞及其培養上清中VEGF錶達均高于對照組(P<0.001);紫草素處理組HaCaT細胞及其培養上清VEGF錶達均低于IL-17處理組(P<0.001);與對照組比較,CCK-8檢測各組HaCaT細胞活力無明顯差異(P>0.05)。結論 IL-17可促進HaCaT細胞分泌VEGF,呈時間依賴型,而紫草素對其具有抑製作用。
목적 관찰백세포개소-17(IL-17)대HaCaT세포분비혈관내피생장인자(VEGF)적영향급자초소적간예작용。방법 수집IL-17자격조화자초소처리후HaCaT세포급기배양토청,분별용쌍항체협심매련면역흡부법(ELISA)급실시형광면역정량-취합매련반응법(RT-PCR)검측VEGF함량。응용세포계수합-8(CCK-8)검측각조HaCaT세포활력。결과 여대조조상비,불동시간IL-17자격조HaCaT세포급기배양상청중VEGF표체균고우대조조(P<0.001);자초소처리조HaCaT세포급기배양상청VEGF표체균저우IL-17처리조(P<0.001);여대조조비교,CCK-8검측각조HaCaT세포활력무명현차이(P>0.05)。결론 IL-17가촉진HaCaT세포분비VEGF,정시간의뢰형,이자초소대기구유억제작용。
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 inhibited the proinflamation 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 realtime 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 control group( P<0.001 ). The expression of VEGF in different drug treatment groups on HaCaT cells and the cell supematant 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 specifically 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 supematant level.