Identification and expression of human CD81 gene on murine NIH/3T3 cell membrane

J Microbiol Methods. 2003 Jul;54(1):81-5. doi: 10.1016/s0167-7012(03)00009-5.

Abstract

The human CD81 (hCD81) molecule has been identified as a putative receptor for hepatitis C virus (HCV). In this study, eukaryotic expression vector pCDM8-hCD81 containing hCD81 cDNA and pSV2neo helper plasmid was used to cotransfect with lipofectamine into murine fibroblast cell line NIH/3T3 to establish an hCD81-expressing cell line. Resistant cell clones were obtained 20 days after the selection with neomycin (600 micro/ml) and then cultured as monoclones. The expression of the transfected hCD81 gene in the cells was verified by RT-PCR and flow cytometry analyses. One of the selected cell clones showed obvious expression of hCD81 and was named NIH/3T3-hCD81. Competitive inhibition tests indicated that the binding of monoclonal anti-hCD81 (JS-81) to NIH/3T3-hCD81 cells was inhibited by recombinant HCV E2 protein, suggesting that the expressed hCD81 molecules on NIH/3T3-hCD81 cells maintain natural conformation of binding to HCV E2. The transfected NIH/3T3-hCD81 cells should be of great potential value in studies on HCV attachment and onset of infection.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Antigens, CD / genetics*
  • Antigens, CD / metabolism*
  • Binding, Competitive
  • Cell Membrane / genetics*
  • Cell Membrane / metabolism
  • Fibroblasts / metabolism*
  • Humans
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism*
  • Mice
  • Tetraspanin 28
  • Transfection*
  • Viral Envelope Proteins / metabolism

Substances

  • Antigens, CD
  • CD81 protein, human
  • Cd81 protein, mouse
  • Membrane Proteins
  • Tetraspanin 28
  • Viral Envelope Proteins
  • glycoprotein E2, Hepatitis C virus