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人外周血淋巴细胞高分辨染色体制备技术的研究
引用本文:张清健,郑立新,田佩玲,叶嘉玲,杨卫,王柏贤,徐珊珊,周冰燚,蔡慧娜,方俊宇,朱志勇.人外周血淋巴细胞高分辨染色体制备技术的研究[J].癌变.畸变.突变,2013,25(1):53-56.
作者姓名:张清健  郑立新  田佩玲  叶嘉玲  杨卫  王柏贤  徐珊珊  周冰燚  蔡慧娜  方俊宇  朱志勇
作者单位:( 广东省计划生育科学技术研究所,广东 广州 510600 )
基金项目:广东省人口和计划生育委员会科研项目(2008009)
摘    要:目的: 建立一种具有分裂指数高和染色体分散好等优点的550~850条带纹高分辨染色体的制备方法。方法:取10例健康人外周血为样本制备淋巴细胞高分辨染色体。固定5-氟尿嘧啶核苷、尿嘧啶核苷、胸腺嘧啶核苷、溴化乙锭、秋水仙胺的剂量,进行5个因素3个水平的正交设计15种实验方案。5个因素分别为培养时间、胸腺嘧啶核苷、溴化乙锭、秋水仙胺作用时间以及低渗时间。3个水平分别为培养时间64、72、80 h;胸腺嘧啶核苷作用时间16、17、18 h;溴化乙锭作用时间3、4、5 h;秋水仙胺作用时间10、15、20 min以及低渗时间30、40、50 min。每例样本同时采用15种方案进行实验,比较各方案带纹在550条以上时染色体分裂指数和分裂相分散的情况。结果:在15种方案中培养时间以及秋水仙胺作用时间对分裂指数有显著影响 (P<0. 01),其中培养72 h后加5-氟尿嘧啶核苷和尿嘧啶核苷进行同步化和秋水仙胺作用15 min高分辨染色体分裂指数最大。37 ℃低渗40 min高分辨染色体分散效果最佳。结论:本实验方案的高分辨染色体制备方法,具有分裂指数高和染色体分散好等优点,具有较好的推广价值。

关 键 词:高分辨染色体  G显带  秋水仙胺  分裂指数
收稿时间:2012-06-29
修稿时间:2012-09-18

The preparation of high-resolution chromosome in human peripheral blood lymphocytes
ZHANG Qing-jian,ZHENG Li-xin,TIAN Pei-ling,YE Jia-ling, YANG Wei,WANG Bai-xian,XU Shan-shan,ZHOU Bing-yi, CAI Hui-na,FANG Jun-yu,ZHU Zhi-yong.The preparation of high-resolution chromosome in human peripheral blood lymphocytes[J].Carcinogenesis,Teratogenesis and Mutagenesis,2013,25(1):53-56.
Authors:ZHANG Qing-jian  ZHENG Li-xin  TIAN Pei-ling  YE Jia-ling  YANG Wei  WANG Bai-xian  XU Shan-shan  ZHOU Bing-yi  CAI Hui-na  FANG Jun-yu  ZHU Zhi-yong
Institution:(Family Planning Research Institute of Guangdong Province, Guangzhou 510600, Guangdong, China)
Abstract:OBJECTIVE: To develop a method for human 550-850 band high-resolution chromosome preparation with advantages such as high mitotic division index and good dispersion rate. METHODS:High-resolution chromosomes were prepared from 10 periphearal blood samples. Doses of 5-fluorouridine,uridine, thymidine,ethidium bromide and demecolcine were constant among 15 experimental designs through arranging 5 factors and 3 standards. 5 factors were adding time of 5-fluorouridine and uridine,action time of thymidine, ethidium bromide and demecolcine. 3 standards referred to addition of 5-fluorouridine and uridine at 64,72 and 80 h,action time of thymidine for 16,17 and 18 h, of ethidium bromide for 3,4 and 5 h,of demecolcine for 10,15 and 20 min,and hypo-osmotic time for 30,40 and 50 min. Each specimen underwent all 15 kinds of treatment designs at the same time. And high-resolution chromosome division index and good dispersion rate were compared among 15 designs. RESULTS:Great significant differences on high-resolution chromosome division index were found from the action time of 5-fluorouridine,uridine and demecolcine(P<0.01).The highest division index of high-resolution chromosome was obtained when cells had been cultured for 72 h before adding 5-fluorouridine and uridine and havested 15 min after adding demecolcine. The best dispersion high-resolution chromosomes could be made when cells had been diluted for 40 min at 37 ℃. CONCLUSION:The method of human high-resolution chromosome preparation from the first experimental design,with advantages such as high cell division index and good dispersion rate,showed great value to be extended to G-banding preparation.
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