NLM Gateway
A service of the U.S. National Institutes of Health
Your Entrance to
Resources from the
National Library of Medicine
    Home      Term Finder      Limits/Settings      Search Details      History      My Locker        About      Help      FAQ    
Skip Navigation Side Barintended for web crawlers only

The carboxy terminus (LLP-1) of the HIV-1 transmembrane glycoprotein gp41 alters glutamate transport in glial cells. Neuroscience of HIV Infection.

Kort JJ.

J Neurovirol. 1998 Jun 3-6; 4: 356.

Department of Medicine, Albany Medical College, NY.

Perturbation of astrocyte functions by HIV-1 infection may contribute to the pathogenesis of AIDS dementia complex. The present study investigated the possibility that astroglial transport of glutamate and aspartate, the major excitatory amino acids (EAA) in the mammalian central nervous system (CNS), is altered by HIV-1 infection. Human U251 glioma cells were infected with the brain isolate SF162 of HIV-1. HIV-1 persisted in glial cells over several months. This nonproductive infection of glial cells was characterized by persistent expression of Nef over the time of the infection, and transient presence of structural viral proteins, including the viral transmembrane glycoprotein gp41, which was detected during the initial two weeks following HIV-1 infection. The presence of gp41 in acutely HIV-1-infected glial cells coincided with a 36% decrease in [3H]-D-aspartate uptake, due to a reduction in the maximal uptake capacity (v(max)) for D-aspartate. The expression of typical astrocytic glutamate transporters EAAT1, and EAAT2 in U251 glioma cells was not altered by HIV-1 infection. To determine whether viral proteins, gp120, gp41, or Nef, were involved in the impairment of EAA transport in acutely HIV-1 infected glial cells, effects of lentiviral lytic peptide type 1 (LLP-1), corresponding to the carboxy terminus of LAI gp41, recombinant SF2 gp120, and recombinant LAI Nef, on [3H]-D-aspartate uptake and on the release of glutamate in glial cells were investigated. Only LLP-1 reduced [3H]-D-aspartate uptake and facilitated the release of glutamate from glial cells in a concentration dependent manner. These results suggest that the carboxy terminus of gp41 impairs EAA transport in glial cells, which may contribute to excitotoxic damage to neurons in HIV-1 infection of the CNS.

Publication Types:
  • Meeting Abstracts
Keywords:
  • AIDS Dementia Complex
  • Amino Acid Transport System X-AG
  • Aspartic Acid
  • Astrocytes
  • Biological Transport
  • Excitatory Amino Acids
  • Glioma
  • Glutamates
  • Glutamic Acid
  • Glycoproteins
  • HIV Envelope Protein gp120
  • HIV-1
  • Humans
  • Neuroglia
  • Neurons
  • Neurosciences
  • education
  • immunology
Other ID:
  • 99930735
UI: 102237429

From Meeting Abstracts




Contact Us
U.S. National Library of Medicine |  National Institutes of Health |  Health & Human Services
Privacy |  Copyright |  Accessibility |  Freedom of Information Act |  USA.gov