A seven-transmembrane domain receptor involved in fusion and entry of T-cell-tropic human immunodeficiency virus type 1 strains

J Virol. 1996 Sep;70(9):6288-95. doi: 10.1128/JVI.70.9.6288-6295.1996.

Abstract

Entry of human immunodeficiency virus type 1 (HIV-1) into cells requires binding to CD4 and fusion with a cellular membrane. Fusion does not occur in most nonhuman cells even when they express human CD4, indicating that one or more human accessory factors are required for virus infection. Recently, a seven-transmembrane domain protein has been shown to serve as an accessory factor for T-cell-tropic (T-tropic) HIV-1 isolates (Y. Feng, C. C. Broder, P. E. Kennedy, and E. A. Berger, Science 272:872-877, 1996). Here we show that expression of this glycoprotein, termed fusin, in murine, feline, simian, and quail cell lines, in conjunction with human CD4, rendered these cells fully permissive for HIV-1 envelope glycoprotein (Env)-mediated membrane fusion. Expression of CD4 or fusin alone did not permit fusion. In addition, introduction of fusin and CD4 into a human cell line, U87MG, that is resistant to HIV-1 induced syncytium formation and to infection by HIV-1 when expressing CD4 alone made this cell line permissive for Env-mediated cell-cell fusion. Fusion was observed only with T-tropic Env proteins. Macrophage-tropic (M-tropic) Env proteins from the SF162, ADA, and Ba-L HIV-1 strains did not fuse with cells expressing fusin and CD4, suggesting that M-tropic viruses utilize an accessory molecule other than fusin. Finally, coexpression of fusin and CD4 made both a murine and feline cell line susceptible to virus infection by T-tropic, but not M-tropic, HIV-1 strains.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antigens, CD / physiology
  • Astrocytoma
  • Base Sequence
  • CD4 Antigens / physiology*
  • Cats
  • Cell Line
  • Cell Membrane / physiology
  • Cell Membrane / ultrastructure
  • Cloning, Molecular
  • Coturnix
  • DNA Primers
  • Fetus
  • Gene Library
  • Gene Products, env / physiology
  • Giant Cells
  • HIV-1 / immunology
  • HIV-1 / physiology*
  • HeLa Cells
  • Humans
  • Membrane Proteins / biosynthesis
  • Membrane Proteins / chemistry
  • Membrane Proteins / physiology*
  • Mice
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Protein Structure, Secondary
  • Receptors, CXCR4
  • Receptors, HIV / physiology*
  • Spleen
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / virology*
  • Tumor Cells, Cultured

Substances

  • Antigens, CD
  • CD4 Antigens
  • DNA Primers
  • Gene Products, env
  • Membrane Proteins
  • Receptors, CXCR4
  • Receptors, HIV