期刊文献+

罗伯逊易位型21三体永生淋巴细胞株的建立 被引量:1

Establishment of immortalized B-lymphoblastoid cell lines of Robertsonian translocation type trisomy 21
原文传递
导出
摘要 目的建立并鉴定13/21易位与21/21罗伯逊易位21三体永生淋巴细胞株,为21三体罗伯逊易位的遗传学研究提供实验材料。方法筛查获得易位型21三体患者并收集外周血,培养B95-8细胞制备EB病毒感染液,采用EB病毒转化法获得永生淋巴细胞株,对第10、15、20代细胞进行G显带染色体分析。结果筛检出1例罕见的13/21易位与4例21/21罗伯逊易位型21三体患儿并成功建立永生淋巴细胞株,传代至第10、15、20代细胞的核型无显著差异。结论 EB病毒转化法可用于易位型21三体永生淋巴细胞株的建立,早期转化的细胞可为该病的研究提供实验基础。 Objective. To establish immortalized B-lymphoblastoid cell lines of Robertsonian translocation type trisomy 21 by Epstein-Barr (EB) virus and conduct karyotype analysis of the cells. Methods: Genetic screening for the Robertsonian translocation type trisomy 21 children; then collection patient' s peripheral blood. Cultivation of B95-8 cells was prepared for EB virus transformation of peripheral blood B lymphocytes. Karyotype analysis was performed for the cultured cells of passages 10, 15, and 20 to evaluate their genetic stability. Results: Screening out a rare case of rob ( 13; 21 ) and 3 cases of rob (21; 21 ) . Altogether 5 immortalized lymphoblastoid cell lines with stable chromosome were obtained successfully from the patients. No chromosomal abnormalities were found in the cultured cells of passages 10, 15, and 20. Conclusion. EB virus can be used in the establishment of immortalized B-lymphoblastoid cell lines of Robertsonian translocation type trisomy 21, this chromosomal disease is studied preferably with. cells of early passages.
出处 《中国优生与遗传杂志》 2014年第12期31-33,共3页 Chinese Journal of Birth Health & Heredity
基金 安徽理工大学2014年大学生科研项目(ZZ140) 国家级大学生创新创业训练计划项目(NO.201310361095) 安徽省教育厅基金(KJ2012A080)
关键词 21-三体 罗伯逊易位 EB病毒 永生淋巴细胞株 Robertsonian translocations Trisomy21 Epstein-Barrvirus B-lymphoblastoid cell lines
  • 相关文献

参考文献8

二级参考文献45

  • 1韩茜,韩阳,陈黎明.唐氏综合征的环境致病因素和遗传因素分析[J].中国优生与遗传杂志,2005,13(9):36-36. 被引量:8
  • 2李立,谭跃球,李麓芸,卢光琇.染色体显带分析结合荧光原位杂交进行产前诊断[J].中华医学遗传学杂志,2006,23(1):120-120. 被引量:3
  • 3于萍,王和,袁粒星.产前诊断技术及其临床应用[J].中国优生与遗传杂志,2007,15(4):14-17. 被引量:37
  • 4戴朴,韩冰,袁永一,金政策,王毅,向阳,于飞,刘新,王国建,康东洋,张昕,李梅,翟所强,黄德亮,韩东一.基于基因诊断的耳聋遗传咨询、指导作用的初步观察[J].中华医学杂志,2007,87(16):1088-1092. 被引量:16
  • 5Kroenberg JR, Kawashima H. Molecular definition of a region of chromosome 21 that cause features of the Down Syndrome phenotype[ J]. Am J Hum Genet, 1990, 47(2) : 236 -246.
  • 6Writters I,Devriendt K,Legius E,et al.Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridization (FISH)[J].Prenat Diagn,2002,22:29-33.
  • 7Down J L H.Observations on an ethnic classification of idiots[J].London Hosp Clin Lect Rep,1866,3:259-262.
  • 8Mc cormick M K,Schinzel A,Petersen M B,et al.Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21[J].Genomics,1989,5(2):325-331.
  • 9Korenberg J R,Chen X N,Daumer C,et al.Down Syndrome phenotypes:the consequences of chromosomal imbalance[J].Pans,1994,91:4997-5001.
  • 10Korenberg J R.Molecular definifion of a region of chromosome 21 the canses feafures of the Down syndrome phenotype[J].Am J Hum Genet,1990,47:236-239.

共引文献31

同被引文献6

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部