Cofactor requirement for human immunodeficiency virus type 1 entry into a CD4-expressing human cell line

J Virol. 1993 Oct;67(10):5939-47. doi: 10.1128/JVI.67.10.5939-5947.1993.

Abstract

Expression of the human immunodeficiency virus type 1 (HIV-1) receptor CD4 on many nonhuman and some human cell lines is not sufficient to permit HIV-1 infection. We describe a human glioblastoma cell line (U373-MG) which remains resistant to HIV-1 despite the added expression of an authentic CD4 molecule. The block to HIV-1 infection of these cells is strain independent and appears to be at viral entry. Heterokaryons of CD4-expressing U373-MG (U373-CD4) cells fused to HeLa cells allow HIV-1 entry. A U373-CD4/HeLa hybrid clone allows efficient HIV-1 replication. These results suggest that HeLa cells express a factor(s) that can complement the viral entry defect of U373-CD4 cells and is necessary for efficient CD4-mediated HIV-1 infection.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antigens, CD / biosynthesis
  • Antigens, CD / isolation & purification
  • Antigens, CD / metabolism*
  • Base Sequence
  • Blotting, Western
  • CD4 Antigens / biosynthesis
  • CD4 Antigens / isolation & purification
  • CD4 Antigens / metabolism*
  • Cell Fusion
  • Electrophoresis, Polyacrylamide Gel
  • Flow Cytometry
  • Glioma
  • HIV Reverse Transcriptase
  • HIV-1 / physiology*
  • HeLa Cells
  • Humans
  • Hybrid Cells
  • Molecular Sequence Data
  • Neoplasm Proteins / isolation & purification
  • Neoplasm Proteins / metabolism
  • Oligodeoxyribonucleotides
  • Polymerase Chain Reaction
  • RNA-Directed DNA Polymerase / analysis
  • RNA-Directed DNA Polymerase / metabolism
  • Recombinant Proteins / analysis
  • Recombinant Proteins / biosynthesis
  • Tumor Cells, Cultured
  • Virus Replication*
  • beta-Galactosidase / analysis
  • beta-Galactosidase / biosynthesis

Substances

  • Antigens, CD
  • CD4 Antigens
  • Neoplasm Proteins
  • Oligodeoxyribonucleotides
  • Recombinant Proteins
  • HIV Reverse Transcriptase
  • RNA-Directed DNA Polymerase
  • beta-Galactosidase