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作 者:张国梁[1] 吴江[1] 关键[1] 关宏[2] 李德超[1] 王心彧[1]
机构地区:[1]佳木斯大学口腔医学院,黑龙江佳木斯154002 [2]齐齐哈尔医学院,黑龙江齐齐哈尔161006
出 处:《黑龙江医药科学》2014年第5期7-10,共4页Heilongjiang Medicine and Pharmacy
基 金:佳木斯大学科学技术面上项目;编号:L2012-034
摘 要:目的:初步研究乳杆菌A-2代谢产物(LSPM1和LSPM2)对人舌鳞癌CAL-27细胞的增殖抑制及诱导细胞凋亡。方法:乳杆菌A-2通过降解制备相应的代谢产物LSPM1和LSPM2;采用MTT法检测不同浓度的LSPM1和LSPM2(1.875mg/mL、3.75mg/mL、7.5mg/mL、15mg/mL和30mg/mL)对CAL-27细胞的体外增殖抑制作用;荧光显微镜下观察CAL-27细胞形态变化;采用流式细胞仪和DNA琼脂凝胶电泳法检测细胞凋亡情况。结果:不同浓度的乳杆菌A-2代谢产物LSPM1和LSPM2可以抑制CAL-27细胞的增殖,呈现明显的浓度依赖性;LPSM1可明显诱导CAL-27细胞凋亡,呈时间依赖性。结论:乳杆菌A-2代谢产物可以在体外抑制人舌鳞癌CAL-27细胞生长增殖,并诱导CAL-27细胞凋亡。Objective. To preliminarily study how lactobacillus sp A--2 metabolites (LSPM1 and LSPM2) restrain human tongue squamous carcinoma CAL--27 cells proliferation and induce its apoptosis. Methods. LSPM1 and LSPM2 were prepared by degradation lactobaeillus sp A--2. It was used to detect different concentrations of LSPM1 and LSPM2 (1. 875mg/mL, 3.75mg/mL, 7.5mg/mL, 15mg/mL, and 30mg/mL) of CAL--27 cells in vitro proliferation inhibition by MTT method. CAL--27 ceil morphological changes were observed by using fluorescence microscope. It was to detect the apoptosis situation of CAL--27 cells by flow cytometry method (FCM) and agarose gel electrophoresis. Results. Different concentrations of LSPM1 and LSPM2 could restrain the growth of CAL--27 cells and had a dose--dependent manner. The apoptosis of CAL --27 cells were obviously induced in time--dependence. Conclusion. Proliferation of CAL--27 cells is inhibited by Lactobaeillus sp A--2 metabolites. Lactobacillus sp A--2 metabolites can induce CAL--27 cells apoptosis.
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