浙江中西医结合杂志
浙江中西醫結閤雜誌
절강중서의결합잡지
ZHEJIANG JOURNAL OF INTEGRATED TRADITIONAL CHINESE AND WESTERN MEDICINE
2014年
1期
14-15,24
,共3页
王少娟%林筱洁%尹利明%高瑞兰
王少娟%林篠潔%尹利明%高瑞蘭
왕소연%림소길%윤리명%고서란
SHI-1细胞%凋亡%七叶皂苷钠
SHI-1細胞%凋亡%七葉皂苷鈉
SHI-1세포%조망%칠협조감납
SHI-1 cells%apoptosis sodium%aescinate
目的:研究七叶皂苷钠对人急性单核白血病细胞株SHI-1细胞的抑制增殖及诱导凋亡的作用。方法 SHI-1细胞经不同浓度的七叶皂苷钠处理后,MTT法分析七叶皂苷钠对SHI-1细胞增殖的抑制作用,Annexin吁/PI染色流式细胞术(FCM)检测细胞凋亡率,DNA凝胶电泳观察凋亡特异性DNA降解梯形条带,半定量PCR检测凋亡特异性酶Caspase-3 mRNA表达水平。结果MTT法显示七叶皂苷钠能显著抑制SHI-1细胞的增殖,呈时间和剂量依赖性(P<0.05)。经不同浓度的七叶皂苷钠处理24h,Annexin吁/PI染色显示Annexin吁阳性的凋亡细胞率明显上升,DNA琼脂糖凝胶电泳分析出现凋亡特异性的DNA降解梯形条带,半定量PCR显示Caspase-3 mRNA表达水平随药物浓度增加而升高(P<0.05)。结论七叶皂苷钠对SHI-1细胞具有抑制增殖和诱导凋亡的作用,可能是其抗白血病作用途径之一。
目的:研究七葉皂苷鈉對人急性單覈白血病細胞株SHI-1細胞的抑製增殖及誘導凋亡的作用。方法 SHI-1細胞經不同濃度的七葉皂苷鈉處理後,MTT法分析七葉皂苷鈉對SHI-1細胞增殖的抑製作用,Annexin籲/PI染色流式細胞術(FCM)檢測細胞凋亡率,DNA凝膠電泳觀察凋亡特異性DNA降解梯形條帶,半定量PCR檢測凋亡特異性酶Caspase-3 mRNA錶達水平。結果MTT法顯示七葉皂苷鈉能顯著抑製SHI-1細胞的增殖,呈時間和劑量依賴性(P<0.05)。經不同濃度的七葉皂苷鈉處理24h,Annexin籲/PI染色顯示Annexin籲暘性的凋亡細胞率明顯上升,DNA瓊脂糖凝膠電泳分析齣現凋亡特異性的DNA降解梯形條帶,半定量PCR顯示Caspase-3 mRNA錶達水平隨藥物濃度增加而升高(P<0.05)。結論七葉皂苷鈉對SHI-1細胞具有抑製增殖和誘導凋亡的作用,可能是其抗白血病作用途徑之一。
목적:연구칠협조감납대인급성단핵백혈병세포주SHI-1세포적억제증식급유도조망적작용。방법 SHI-1세포경불동농도적칠협조감납처리후,MTT법분석칠협조감납대SHI-1세포증식적억제작용,Annexin우/PI염색류식세포술(FCM)검측세포조망솔,DNA응효전영관찰조망특이성DNA강해제형조대,반정량PCR검측조망특이성매Caspase-3 mRNA표체수평。결과MTT법현시칠협조감납능현저억제SHI-1세포적증식,정시간화제량의뢰성(P<0.05)。경불동농도적칠협조감납처리24h,Annexin우/PI염색현시Annexin우양성적조망세포솔명현상승,DNA경지당응효전영분석출현조망특이성적DNA강해제형조대,반정량PCR현시Caspase-3 mRNA표체수평수약물농도증가이승고(P<0.05)。결론칠협조감납대SHI-1세포구유억제증식화유도조망적작용,가능시기항백혈병작용도경지일。
Objective To investigate the effects of sodium aescinate on inhibiting proliferation and inducing apoptosis of human acute monocytic leukemic SHI-1 cells. Methods Proliferation of sodium aescinate treated SHI-1 cells was detected by MTT method. The apoptosis rates of SHI-1 cells were analyzed by flow cytometry af-ter annexin V/PI staining. The gel electrophoresis of DNA ladder was used to analyze the bands of DNA degrada-tion, and the expression level of caspase-3 mRNA was tested by reverse transcription-polymerase chain reaction (RT-PCR). Results MTT assay showed that the proliferation of SHI-1 cells was effectively inhibited by sodium aescinate in a time-and-does dependent manner(P<0.05). The Annexinⅴ positive rate of SHI-1 cells after treated with sodium aescinate was significantly increased by FCM analysis(P<0.05). The apoptosis typical DNA fragments of SHI-1 cells treated with sodium aescinate was presented on the gel electrophoresis. The expression level of cas-pase-3 mRNA was up-regulated with increasing concentration of sodium aescinate by RT-PCR detection(P<0.05). Con-clusion Treatment with sodium aescinate can have inhibitory effect on proliferation and induce apoptosis of SHI-1 leukemia cells. Our results provides an experimental evidence for the activity of sodium aescinate on anti-leukemia.