北京医学
北京醫學
북경의학
BEIJING MEDICAL JOURNAL
2009年
12期
739-742
,共4页
朱鸣%吴本俨%聂捷琳%李莹辉
硃鳴%吳本儼%聶捷琳%李瑩輝
주명%오본엄%섭첩림%리형휘
模拟失重%胃癌细胞%胃黏膜上皮细胞%细胞增殖%细胞周期
模擬失重%胃癌細胞%胃黏膜上皮細胞%細胞增殖%細胞週期
모의실중%위암세포%위점막상피세포%세포증식%세포주기
Simulated weightlessness%Gastric carcinoma cells%Gastric mucosa cells%Cell proliferation Cell cycle
目的 探讨模拟失重对胃癌SGC-7901细胞和胃黏膜上皮HFE-145细胞增殖和周期的影响.方法 采用回转器模拟失重,两种细胞各分为两组,回转组和1G对照组,实验时间共72h.采用免疫组化法观察两种细胞增殖核抗原(proliferating cell nuclear antigen,PCNA)表达的变化,应用流式细胞仪测定细胞周期.结果 与对照组相比,回转组SGC-7901细胞48h及72h PCNA抗体阳性率明显减少(P<0.05及P<0.01),G0+G1期细胞显著增多(P<0.01及P<0.05):12h、24h及36h PCNA抗体阳性细胞的比率无显著性差异.与对照组相比,回转组HFE-145细胞12hPCNA抗体阳性率明显减少(P<0.05),G0+G1期细胞显著增多(P<0.05).结论 回转器模拟失重使胃癌SGC-7901细胞48h及72h时出现细胞周期阻滞、增殖抑制.胃黏膜上皮HFE-145细胞在12h时出现上述变化.
目的 探討模擬失重對胃癌SGC-7901細胞和胃黏膜上皮HFE-145細胞增殖和週期的影響.方法 採用迴轉器模擬失重,兩種細胞各分為兩組,迴轉組和1G對照組,實驗時間共72h.採用免疫組化法觀察兩種細胞增殖覈抗原(proliferating cell nuclear antigen,PCNA)錶達的變化,應用流式細胞儀測定細胞週期.結果 與對照組相比,迴轉組SGC-7901細胞48h及72h PCNA抗體暘性率明顯減少(P<0.05及P<0.01),G0+G1期細胞顯著增多(P<0.01及P<0.05):12h、24h及36h PCNA抗體暘性細胞的比率無顯著性差異.與對照組相比,迴轉組HFE-145細胞12hPCNA抗體暘性率明顯減少(P<0.05),G0+G1期細胞顯著增多(P<0.05).結論 迴轉器模擬失重使胃癌SGC-7901細胞48h及72h時齣現細胞週期阻滯、增殖抑製.胃黏膜上皮HFE-145細胞在12h時齣現上述變化.
목적 탐토모의실중대위암SGC-7901세포화위점막상피HFE-145세포증식화주기적영향.방법 채용회전기모의실중,량충세포각분위량조,회전조화1G대조조,실험시간공72h.채용면역조화법관찰량충세포증식핵항원(proliferating cell nuclear antigen,PCNA)표체적변화,응용류식세포의측정세포주기.결과 여대조조상비,회전조SGC-7901세포48h급72h PCNA항체양성솔명현감소(P<0.05급P<0.01),G0+G1기세포현저증다(P<0.01급P<0.05):12h、24h급36h PCNA항체양성세포적비솔무현저성차이.여대조조상비,회전조HFE-145세포12hPCNA항체양성솔명현감소(P<0.05),G0+G1기세포현저증다(P<0.05).결론 회전기모의실중사위암SGC-7901세포48h급72h시출현세포주기조체、증식억제.위점막상피HFE-145세포재12h시출현상술변화.
Objective To investigate the effects of simulated weightlessness on cell proliferation and cell cycle of human gastric carcinoma cell line SGC-7901 and human gastric mucosa cell line HFE-145. Methods A rotating clinostat was used to simulate weightlessness. Every cell line was divided into two groups, one was rotating group, the other was 1G control group. The whole experimental session was 72h. The expressions of PCNA(proliferating cell nuclear antigen) were examined by immunohistochemical stain. The changes of cell cycle were examined by a cytometer. Results Compared with the control group, the cell proliferation of SGC-7901 cell was inhibited in 48h and 72h in the rotating group, and the cell conversion from G1 to S phase was suppressed. Compared with the control group, the cell proliferation of HFE-145 cell was inhibited in 12h in the rotating group, and the cell conversion from Gl to S phase was suppressed. Conclusions the cell proliferation of SGC-7901 cell is inhibited in 48h and 72h during simulated weightlessness by a clinostat, but HFE-145 cells only have present those above-mentioned changes in 12h during simulated weightlessness by a clinostat.