国际放射医学核医学杂志
國際放射醫學覈醫學雜誌
국제방사의학핵의학잡지
International Journal of Radiation Medicine and Nuclear Medicine
2015年
5期
385-388
,共4页
董娟聪%刘红艳%党旭红%原雅艺%张慧芳%王超%段志凯%左雅慧
董娟聰%劉紅豔%黨旭紅%原雅藝%張慧芳%王超%段誌凱%左雅慧
동연총%류홍염%당욱홍%원아예%장혜방%왕초%단지개%좌아혜
重离子%γ射线%淋巴细胞%辐射%生物效应
重離子%γ射線%淋巴細胞%輻射%生物效應
중리자%γ사선%림파세포%복사%생물효응
Heavy ions%Gamma rays%Lymphocytes%Radiation%Biological effect
目的 比较12C重离子与γ射线对人外周血淋巴细胞Peng-EBV增殖抑制率、细胞周期和凋亡率的影响.方法 对Peng-EBV细胞分别进行2.0 Gy的12C重离子和γ射线照射,通过MTS法检测细胞增殖变化,流式细胞术检测细胞凋亡率和周期分布.结果 2.0Gy重离子射线和γ射线作用后,Peng-EBV细胞的增殖抑制率均显著升高.与对照组相比,2.0 Gy射线照射后24、48、72 h细胞增殖抑制率差异有统计学意义(重离子射线:t=10.53、4.11、37.30,P<0.05;γ射线:t=7.18、8.26、26.11,P<0.05).12C重离子对细胞的增殖抑制率在照射后72 h内呈时间依赖性升高,而γ射线则在照射后48h时增殖抑制率最高,而后降低.重离子射线照射后12h和24h,细胞凋亡率分别较对照组增加了7.92和13.41倍(t=7.09、4.13,P<0.05);而γ射线照射后12 h和24 h,细胞凋亡率分别为对照组的2.43和5.64倍(t=8.98、20.52,P<0.05).重离子射线照射后12h和24 h,细胞G2/M期阻滞程度分别较对照组增加5.11和11.77倍(t=12.06、100.08,P<0.05);而γ射线照射后12 h和24 h,细胞G2/M期阻滞程度分别为对照组的5.82和7.68倍(t=19.35、10.30,P<0.05).结论 12C重离子对人外周血淋巴细胞造成的生物学效应远高于γ射线.
目的 比較12C重離子與γ射線對人外週血淋巴細胞Peng-EBV增殖抑製率、細胞週期和凋亡率的影響.方法 對Peng-EBV細胞分彆進行2.0 Gy的12C重離子和γ射線照射,通過MTS法檢測細胞增殖變化,流式細胞術檢測細胞凋亡率和週期分佈.結果 2.0Gy重離子射線和γ射線作用後,Peng-EBV細胞的增殖抑製率均顯著升高.與對照組相比,2.0 Gy射線照射後24、48、72 h細胞增殖抑製率差異有統計學意義(重離子射線:t=10.53、4.11、37.30,P<0.05;γ射線:t=7.18、8.26、26.11,P<0.05).12C重離子對細胞的增殖抑製率在照射後72 h內呈時間依賴性升高,而γ射線則在照射後48h時增殖抑製率最高,而後降低.重離子射線照射後12h和24h,細胞凋亡率分彆較對照組增加瞭7.92和13.41倍(t=7.09、4.13,P<0.05);而γ射線照射後12 h和24 h,細胞凋亡率分彆為對照組的2.43和5.64倍(t=8.98、20.52,P<0.05).重離子射線照射後12h和24 h,細胞G2/M期阻滯程度分彆較對照組增加5.11和11.77倍(t=12.06、100.08,P<0.05);而γ射線照射後12 h和24 h,細胞G2/M期阻滯程度分彆為對照組的5.82和7.68倍(t=19.35、10.30,P<0.05).結論 12C重離子對人外週血淋巴細胞造成的生物學效應遠高于γ射線.
목적 비교12C중리자여γ사선대인외주혈림파세포Peng-EBV증식억제솔、세포주기화조망솔적영향.방법 대Peng-EBV세포분별진행2.0 Gy적12C중리자화γ사선조사,통과MTS법검측세포증식변화,류식세포술검측세포조망솔화주기분포.결과 2.0Gy중리자사선화γ사선작용후,Peng-EBV세포적증식억제솔균현저승고.여대조조상비,2.0 Gy사선조사후24、48、72 h세포증식억제솔차이유통계학의의(중리자사선:t=10.53、4.11、37.30,P<0.05;γ사선:t=7.18、8.26、26.11,P<0.05).12C중리자대세포적증식억제솔재조사후72 h내정시간의뢰성승고,이γ사선칙재조사후48h시증식억제솔최고,이후강저.중리자사선조사후12h화24h,세포조망솔분별교대조조증가료7.92화13.41배(t=7.09、4.13,P<0.05);이γ사선조사후12 h화24 h,세포조망솔분별위대조조적2.43화5.64배(t=8.98、20.52,P<0.05).중리자사선조사후12h화24 h,세포G2/M기조체정도분별교대조조증가5.11화11.77배(t=12.06、100.08,P<0.05);이γ사선조사후12 h화24 h,세포G2/M기조체정도분별위대조조적5.82화7.68배(t=19.35、10.30,P<0.05).결론 12C중리자대인외주혈림파세포조성적생물학효응원고우γ사선.
Objective To compare the effects of carbon heavy ion and γ ray on cell survival, cell cycle and cell apoptosis.Methods Peng-EBV cells were irradiated by carbon heavy ion and X-ray.MTS was used to detect the cell survival.Cell cycle and apoptosis were analyzed by flow cytometry.Results The proliferation inhibition rate of Peng-EBV cell was significantly increased after 2.0 Gy heavy ion rays and γ rays.Compared with the control group, the cell proliferation inhibition rate difference was statistically significant after 2.0 Gy rays at 24 h, 48 h, 72 h (heavy rays: t=10.53, 4.11, 37.30, all P<0.05;γ rays: t=7.18, 8.26, 26.11, all P<0.05).The cell proliferation inhibition rate showed a time-dependent increase, and reached its peak at 72 h after heavy ion rays, while the cell proliferation inhibition rate after γ ray reached its peak at 48 h, and then decreased.Compared with the control group, the apoptosis rate of Peng-EBV cell increased 7.92 and 13.41 times respectively at 12 h and 24 h after 2.0 Gy heavy ion rays (t=7.09, 4.13, both P<0.05), while it was 2.43 and 5.64 times after 2.0 Gy γ rays (t=8.98, 20.52, P< 0.05).Compared with the control group, the G2/M phase arrest increased 5.11 and 11.77 times respectively at 12 h and 24 h after 2.0 Gy heavy ion rays (t=12.06, 100.08, both P<0.05), however, it was 5.82 and 7.68 times after 2.0 Gy γ rays(t=19.35, 10.30, both P<0.05).Conclusion 12C heavy ion irradiation shows more stronger biological effects on human peripheral blood lymphocyte than γ ray.