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郭淑丽, 罗先道, 杨丽, 程建兵, 杨磊. 抗砷细胞内荧光物质激光共聚焦显微镜检测[J]. 中国公共卫生, 2009, 25(6): 710-711. DOI: 10.11847/zgggws2009-25-06-35
引用本文: 郭淑丽, 罗先道, 杨丽, 程建兵, 杨磊. 抗砷细胞内荧光物质激光共聚焦显微镜检测[J]. 中国公共卫生, 2009, 25(6): 710-711. DOI: 10.11847/zgggws2009-25-06-35
GUO Shu-li, LUO Xian-dao, YANG Li, . Detection of fluorescent material in arsenic-resistant cells with LSCM[J]. Chinese Journal of Public Health, 2009, 25(6): 710-711. DOI: 10.11847/zgggws2009-25-06-35
Citation: GUO Shu-li, LUO Xian-dao, YANG Li, . Detection of fluorescent material in arsenic-resistant cells with LSCM[J]. Chinese Journal of Public Health, 2009, 25(6): 710-711. DOI: 10.11847/zgggws2009-25-06-35

抗砷细胞内荧光物质激光共聚焦显微镜检测

Detection of fluorescent material in arsenic-resistant cells with LSCM

  • 摘要: 目的 应用激光共聚焦显微镜检测抗砷细胞内荧光物质含量。方法 用荧光染料Rhodamine-123对抗砷细胞进行荧光染色30min,分别用维拉帕米(Verapamil)、亚砷酸钠处理细胞,单纯Rhodamine-123的抗砷细胞为对照组。应用激光共聚焦显微镜采集Rhodamine-123的荧光图像动态序列,并且记录12,24,36,48,60h等不同时段细胞内荧光强度。结果 实验组细胞染色48h后,Verapamil实验组荧光强度分别为(38.940±0.3648),(38.153±0.533),均明显高于同时间段对照组的荧光强度,差异均有统计学意义(均P<0.05)。结论 激光共聚焦显微成像技术可用于抗砷细胞拮抗效果实时定量检测。

     

    Abstract: Objective To detect the fluore scentmaterial with in arsenic-resistant cells by lase rscanning confocalmicro scope(LSCM).Methods The arsenic-resistant cells were incubated with fluorescent dyes Rhodamine-123 for 30 minutes.The cells of test group were coincubated with Verapamil and NaSO2,respectively.The cells of control group were merely administrated with Rhodamine 123.Fluo rescence miage acquisition of Rhodamine-123s' dynamic series were executed with LSCM,and the concentration fluorescence intracell at different time(12,24,36,48,64h)was recorded.Results After fluo rescence staining for 48h,the fluorescence intensity of the test group was 38.94±0.3648 and 38.153±0.533 for Verapamil and NaSO2 treamtent.The intensities were significantly higher than that of the synchrono us control group.Conclusion The LSCM could be used to detect fluorescent material in arsenic resistant cells tmiely and quantitively.

     

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