Extremely efficient gene transfection into lympho-hematopoietic cell lines by Epstein-Barr virus-based vectors

J Immunol Methods. 1997 May 26;204(2):143-51. doi: 10.1016/s0022-1759(97)00036-7.

Abstract

We have estimated the efficiency of Epstein-Barr virus (EBV)-based vectors in transfecting genes into cell lines of lympho-hematopoietic lineages. The transfection efficiency was estimated both at transient and stable phases, in terms of expression of a marker gene and acquisition of drug resistance, respectively. Plasmid vectors carrying EBV oriP (replication origin of plasmid), EBNA (EBV nuclear antigen)-1 and as the marker genes, murine CD8 alpha cDNA and neoR (neomycin resistant) genes were transfected into various cell lines by electroporation. When cell lines constitutively expressing EBNA-1 were transduced, virtually all the cells expressed CD8 alpha on day 3 and acquired G418 resistance thereafter. In the case of K562 cells, which do not express EBNA-1, approximately 40% of cells expressed the marker gene product on day 3 posttransfection, and 30% of cells became stable transfectants. These data suggest a broader application of the EBV vector system in basic immunology and medicine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Epstein-Barr Virus Nuclear Antigens / analysis
  • Genetic Vectors*
  • Herpesvirus 4, Human / genetics*
  • Humans
  • Transfection*

Substances

  • Epstein-Barr Virus Nuclear Antigens