荧光标记人卵巢癌细胞株的建立
CSTR:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

基金项目:

国家重点基础研究发展计划(“973”计划,2011CB707902).


Establishment of a fluorescence-labeled human ovarian cancer cell line
Author:
Affiliation:

Fund Project:

Supported by National Key Basic Research Development Program (“973” Program,2011CB707902).

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    目的建立稳定高表达增强型绿色荧光蛋白(EGFP)的人卵巢癌细胞株。方法采用基因转染的方法,将EGFP基因导入人卵巢癌细胞HO8910PM中,通过G418筛选、亚克隆扩增获得稳定表达绿色荧光蛋白的EGFP-HO8910PM细胞株,并用流式细胞术检测所获细胞株的EGFP表达率,通过细胞生长曲线、黏附实验、侵袭迁移实验比较EGFP-HO8910PM细胞和HO8910PM细胞的生物学行为。结果筛选出的EGFP-HO8910PM细胞经流式细胞仪检测EGFP阳性表达率达99%以上,EGFP-HO8910PM细胞和HO8910PM细胞生长、黏附及侵袭迁移能力无统计学差异。结论成功建立了稳定表达EGFP且保持母株细胞特性的人卵巢癌细胞株EGFP-HO8910PM,为人卵巢癌整体活体应用中可视化研究打下基础。

    Abstract:

    ObjectiveTo establish a human ovarian cancer cell line stably expressing enhanced green fluorescent protein(EGFP), so as to carry out visualized research on whole ovarian cancer. MethodsWe transfected human ovarian cancer cell line HO8910PM by gene transfection, and obtained cells stably expressing EGFP by sub-cloning amplification and selection with G418-resistance.The expression rate of EGFP was analyzed by flow cytometry (FC).The growth curve, adhesion, migration and invasion experiments were employed to study the biological behaviors of the cells transfected with EGFP. ResultsFlow cytometry results showed that EGFP positive rate of screened EGFP-HO8910PM cells was higher than 99%. The cell growth, adhesion, invasion and migration abilities of cells were not significantly changed after transfection. ConclusionWe have successfully established a cell line EGFP-HO8910PM stably expressing EGFP and at mean time maintaining the characteristics of the parent cell line, which lays a foundation for whole-body visualization research of human ovarian cancer in vivo.

    参考文献
    相似文献
    引证文献
相关视频

分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2012-04-27
  • 最后修改日期:2012-07-17
  • 录用日期:2012-09-19
  • 在线发布日期: 2012-09-24
  • 出版日期:
文章二维码
重要通知
友情提醒: 近日发现论文正式见刊或网络首发后,有人冒充我刊编辑部名义给作者发邮件,要求添加微信,此系诈骗行为!可致电编辑部核实:021-81870792。
            《海军军医大学学报》编辑部
关闭