世界中西医结合杂志
世界中西醫結閤雜誌
세계중서의결합잡지
WORLD JOURNAL OF TRADITIONAL CHINESE AND WESTERN MEDICINE
2015年
5期
623-626
,共4页
杜娜%李健%刘福生%刘泽洲%许可嘉%张寅%刘婷%苏泽琦%丁霞
杜娜%李健%劉福生%劉澤洲%許可嘉%張寅%劉婷%囌澤琦%丁霞
두나%리건%류복생%류택주%허가가%장인%류정%소택기%정하
雷公藤红素%细胞迁移%AGS 细胞%不同浓度%不同时间
雷公籐紅素%細胞遷移%AGS 細胞%不同濃度%不同時間
뢰공등홍소%세포천이%AGS 세포%불동농도%불동시간
Celastrol%Cell migration%AGS cell%Different concentrations%Different times
目的:观察不同浓度雷公藤红素在不同时间对 AGS 细胞形态及细胞迁移的影响,探索雷公藤红素对 AGS 细胞迁移较佳抑制作用浓度及时间。方法将 AGS 细胞铺于6孔板并培养,待贴壁细胞密度达到70%~80%后,采用划痕法制造细胞迁移模型,分为 DMSO 及雷公藤红素5μM、1μM、0.5μM、0.1μM、0.01μM 浓度组,并分别于0 h、6 h、12 h、24 h 观察细胞的形态及细胞的迁移情况,且拍照记录,计算细胞迁移速度及细胞迁移抑制率并进行各组之间的比较。结果高浓度雷公藤红素使 AGS 细胞形态发生改变;雷公藤红素能够抑制 AGS 细胞迁移,且终浓度为1μM 时抑制作用最明显。同一浓度不同作用时间其对 AGS 细胞迁移的抑制作用差异有统计学意义(P ﹤0.05);同一时间不同浓度雷公藤红素对 AGS 细胞迁移的抑制作用差异有统计学意义(P ﹤0.05)。结论高浓度雷公藤红素能够使 AGS 细胞形态发生改变并凋亡;雷公藤红素抑制了 AGS 细胞的迁移,且该抑制作用与浓度、时间相关,且在终浓度为1μM 作用于 AGS 细胞12 h 时,其对 AGS 细胞迁移的抑制作用最明显。
目的:觀察不同濃度雷公籐紅素在不同時間對 AGS 細胞形態及細胞遷移的影響,探索雷公籐紅素對 AGS 細胞遷移較佳抑製作用濃度及時間。方法將 AGS 細胞鋪于6孔闆併培養,待貼壁細胞密度達到70%~80%後,採用劃痕法製造細胞遷移模型,分為 DMSO 及雷公籐紅素5μM、1μM、0.5μM、0.1μM、0.01μM 濃度組,併分彆于0 h、6 h、12 h、24 h 觀察細胞的形態及細胞的遷移情況,且拍照記錄,計算細胞遷移速度及細胞遷移抑製率併進行各組之間的比較。結果高濃度雷公籐紅素使 AGS 細胞形態髮生改變;雷公籐紅素能夠抑製 AGS 細胞遷移,且終濃度為1μM 時抑製作用最明顯。同一濃度不同作用時間其對 AGS 細胞遷移的抑製作用差異有統計學意義(P ﹤0.05);同一時間不同濃度雷公籐紅素對 AGS 細胞遷移的抑製作用差異有統計學意義(P ﹤0.05)。結論高濃度雷公籐紅素能夠使 AGS 細胞形態髮生改變併凋亡;雷公籐紅素抑製瞭 AGS 細胞的遷移,且該抑製作用與濃度、時間相關,且在終濃度為1μM 作用于 AGS 細胞12 h 時,其對 AGS 細胞遷移的抑製作用最明顯。
목적:관찰불동농도뢰공등홍소재불동시간대 AGS 세포형태급세포천이적영향,탐색뢰공등홍소대 AGS 세포천이교가억제작용농도급시간。방법장 AGS 세포포우6공판병배양,대첩벽세포밀도체도70%~80%후,채용화흔법제조세포천이모형,분위 DMSO 급뢰공등홍소5μM、1μM、0.5μM、0.1μM、0.01μM 농도조,병분별우0 h、6 h、12 h、24 h 관찰세포적형태급세포적천이정황,차박조기록,계산세포천이속도급세포천이억제솔병진행각조지간적비교。결과고농도뢰공등홍소사 AGS 세포형태발생개변;뢰공등홍소능구억제 AGS 세포천이,차종농도위1μM 시억제작용최명현。동일농도불동작용시간기대 AGS 세포천이적억제작용차이유통계학의의(P ﹤0.05);동일시간불동농도뢰공등홍소대 AGS 세포천이적억제작용차이유통계학의의(P ﹤0.05)。결론고농도뢰공등홍소능구사 AGS 세포형태발생개변병조망;뢰공등홍소억제료 AGS 세포적천이,차해억제작용여농도、시간상관,차재종농도위1μM 작용우 AGS 세포12 h 시,기대 AGS 세포천이적억제작용최명현。
Objective To observe the effects of different concentration of celastrol on cellular mor-phology and migration of AGS cells at different time points;to explore a better inhibitory effect of concentra-tion and time of celastrol on migration of AGS cells. Methods AGS cells were planted and cultured in 6 -well plate. When the adherent cell density reached 70 ~ 80% ,cell migration was manufactured by scratch ex-periment. Thereafter,cell morphology and cell migration were observed under microscope with different con-centration of celastrol of 5 μM、1 μM、0. 5 μM、0. 1 μM、0. 01 μM at indicated time points. Results 1. High concentration of celastrol cause severe changed in the cell morphology. 2. Celastrol inhibited AGS cell migra-tion,and its inhibitory effect on the migration velocity was concentration - dependent in a certain range. The higher the concentration of drug,the stronger effect it was. The same concentration of celastrol on AGS cells at different times had different effect inhibition of cell migration(P ﹤ 0. 05). At the same time the different con-centrations of celastrol on AGS cells had different effect inhibition of cell migration(P ﹤ 0. 05). Conclusion 1. High concentrations of celastrol cause changes in the cell morphology and cell apoptosis. 2. Celastrol in-hibited AGS cell migration,which is dependent on the concentration and action time. The inhibitory effect of celastrol on AGS cell migration is most obvious under final concentration of 1 μM at 12 h.