微孔板成像系统在高表达荧光蛋白单克隆细胞株筛选中的应用研究
DOI:
作者:
作者单位:

南京医科大学

作者简介:

通讯作者:

中图分类号:

基金项目:

国家科技重大专项;2023年度江苏省大型科学仪器开放共享自主研究课题备案课题


The Application of a Microplate Imaging System in Screening Monoclonal Cell Lines with High Fluorescence Protein Expression
Author:
Affiliation:

Nanjing medical university

Fund Project:

  • 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:建立利用微孔板成像系统筛选稳定转染后的高表达荧光蛋白的单克隆细胞株的筛选流程。方法:HBE细胞利用慢病毒稳定转染GFP,经流式细胞术分选荧光信号强的细胞入黑壁透明底的96孔板。除1个孔分选50个细胞入孔(用于成像参数的设定),其余95孔均分选1个细胞入孔。根据筛选流程,4次利用微孔板成像系统的成像和分析功能对95个孔进行逐步筛选。分选当天筛选出含有单细胞的孔,克隆团形成后筛选出能长出克隆团的孔。筛选出的孔内的细胞各自消化并转移至新孔后,再筛选出细胞平均荧光强度较强的孔。细胞增殖至消化后的4-8倍时,筛选出细胞能正常增殖的孔。最终用流式细胞术、荧光成像比较筛选出来的孔内的单克隆细胞株与原细胞的荧光强度。结果:按照筛选流程,依次筛选出89个含有单细胞的孔,19个能长出克隆团的孔,6个细胞平均荧光强度较强的孔,3个细胞能正常增殖的孔。筛选出的来源于这三个孔的单克隆细胞株的平均荧光强度和荧光强的细胞百分比较原细胞均显著提高。结论:利用微孔板成像系统的成像和分析功能,按照筛选流程逐步筛选经稳定转染后的高表达荧光蛋白的单克隆细胞株,与传统的显微镜观察/成像相比,其筛选步骤简单、方便,具有一定的推广应用价值。

    Abstract:

    Objective: To establish a program for screening monoclonal cell lines with high expression of fluorescent protein after stable transfection using a microplate imaging system. Methods: HBE cells were stably transfected with GFP (green fluorescent protein) by lentivirus and cells with high fluorescence intensity were seeded into a 96-well black plate (with clear bottom) by flow cytometric sorting. Single cells were seeded into all wells, except one well, into which 50 cells were seeded to acquire an appropriate setting during imaging. According to the screening protocol, the imaging and analysis functions of the microplate imaging system were employed four times to perform screening across 95 wells. Wells containing one single cell were picked out on the day of sorting and wells containing cell colonies were picked out after clone formation. After cells in the selected wells were individually disassociated and cultured in new wells, wells containing cells with high fluorescence intensity were picked out. After achieving 4-8× population expansion, wells containing cells exhibiting normal proliferative capacity were picked out. The fluorescence intensities of selected monoclonal cell lines were ultimately confirmed by flow cytometry and fluorescence imaging. Results: According to the screening program, 89 wells containing one single cell, 19 wells containing cell colonies, 6 wells containing cells with high fluorescence intensity and 3 wells containing cells exhibiting normal proliferative capacity were picked out sequentially. The selected cell lines from those 3 wells exhibited significantly higher mean fluorescence intensities and higher percentages of cells with strong fluorescence, compared to parental cells. Conclusion: Application of a microplate imaging system to the screening of monoclonal cell lines with high expression of fluorescent protein after stable transfection, based on the screening program, is simple and convenient (compared with traditional microscopy-based observation/imaging), showing considerable potential for widespread application.

    参考文献
    相似文献
    引证文献
引用本文
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:2025-07-04
  • 最后修改日期:2025-10-29
  • 录用日期:2026-03-03
  • 在线发布日期:
  • 出版日期:
关闭