Skip to main content

Advertisement

Log in

Central nervous system damage produced by expression of the HIV-1 coat protein gpl20 in transgenic mice

  • Letter
  • Published:

From Nature

View current issue Submit your manuscript

Abstract

MANY people infected with human immunodeficiency virus type 1 (HIV-1) develop neurological complications that can culminate in dementia and paralysis1. The discrepancy between the severity of impairment and the paucity of detectable HIV-1 within neurons has led to an intense search for diffusible virus- and host-derived factors that might be neurotoxic (see ref. 2 for review). The HIV-1 envelope glycoprotein gp120 is an extracellular protein that is shed from infected cells3 and so has the potential to diffuse and interact with distant uninfected brain cells. Studies on cultured immature cells suggest that gp120 induces neurotoxicity (reviewed in refs 2, 4), and systemic injection of gp120 in neonatal rats5 and intracerebroventricular injection in adult rats results in deleterious effects on the brain6,7. To assess the pathogenic potential of gp120 in the intact brain, we have now produced gp120 in the brains of transgenic mice and found a spectrum of neuronal and glial changes resembling abnormalities in brains of HIV-1-infected humans. The severity of damage correlated positively with the brain level of gp120 expression. These results provide in vivo evidence that gp120 plays a key part in HIV-1-associated nervous system impairment. This model should facilitate the evaluation and development of therapeutic strategies aimed at HIV–brain interactions.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Working Group of the American Academy of Neurology AIDS Task Force. Neurology 41, 778–785 (1991).

  2. Spencer, D. C. & Price, R. W. A. Rev. Microbiol. 46, 655–693 (1992).

    Article  CAS  Google Scholar 

  3. Schneider, J., Kaaden, O., Copeland, T. D., Oroszlan, S. & Hunsmann, G. J. gen. Virol. 67, 2533–2538 (1986).

    Article  CAS  Google Scholar 

  4. Epstein, L. G. & Gendelman, H. E. Ann. Neurol. 33, 429–436 (1993).

    Article  CAS  Google Scholar 

  5. Hill, J. M., Mervis, R. F., Avidor, R., Moody, T. W. & Brenneman, D. E. Brain. Res. 603, 222–223 (1993).

    Article  CAS  Google Scholar 

  6. Kimes, A. S., London, E. D., Szabo, G., Raymon, L. & Tabakoff, B. Expl Neurol. 112, 224–228 (1991).

    Article  CAS  Google Scholar 

  7. Glowa, J. R. et al. Brain Res. 570, 49–53 (1992).

    Article  CAS  Google Scholar 

  8. Mucke, L., Oldstone, M. B. A., Morris, J. C. & Nerenberg, M. I. New Biol. 3, 465–474 (1991).

    CAS  PubMed  Google Scholar 

  9. Mucke, L. et al. Neurobiol. Aging 13, Suppl. 1, S101 (1992).

    Google Scholar 

  10. Campbell, I. L. et al. Proc. natn. Acad. Sci. U.S.A. 90, 10061–10065 (1993).

    Article  ADS  CAS  Google Scholar 

  11. Masliah, E. et al. Ann. Neurol. 32, 321–329 (1992).

    Article  CAS  Google Scholar 

  12. Wiley, C. A. et al. Ann. Neurol. 29, 651–657 (1991).

    Article  CAS  Google Scholar 

  13. Lipton, S. A. NeuroReport 3, 913–915 (1992).

    Article  CAS  Google Scholar 

  14. Giulian, D., Wendt, E., Vaca, K. & Noonan, C. A. Proc. natn. Acad. Sci. U.S.A. 90, 2769–2773 (1993).

    Article  ADS  CAS  Google Scholar 

  15. Eddleston, M. P. & Mucke, L. Neuroscience 54, 15–36 (1993).

    Article  CAS  Google Scholar 

  16. Budka, H. Brain. Path. 1, 163–175 (1991).

    Article  CAS  Google Scholar 

  17. Abraham, C. R., Kanemaru, K. & Mucke, L. Brain Res. 621, 222–232 (1993).

    Article  CAS  Google Scholar 

  18. Mucke, L. & Eddleston, M. FASEB J. 7, 1226–1232 (1993).

    Article  CAS  Google Scholar 

  19. Dickson, D. W., Lee, S. C., Mattiace, L. A., Yen, S.-H. C. & Brosnan, C. Glia 7, 75–83 (1993).

    Article  CAS  Google Scholar 

  20. Mucke, L. & Rockenstein, E. M. Transgene 1, 3–9 (1993).

    Google Scholar 

  21. Campbell, I. L., Mucke, L. & Sandberg, K. Soc. Neurosci. Abstr. 19, 98.2 (1993).

    Google Scholar 

  22. Freed, E. O., Myers, D. J. & Risser, R. J. Virol. 63, 4670–4675 (1989).

    CAS  PubMed  PubMed Central  Google Scholar 

  23. Miura, M., Tamura, T. & Mikoshiba, K. J. Neurochem. 55, 1180–1188 (1990).

    Article  CAS  Google Scholar 

  24. McCune, J. M. et al. Cell 53, 55–67 (1988).

    Article  CAS  Google Scholar 

  25. Haass, C., Hung, A. Y. & Selkoe, D. J. J. Neurosci. 11, 3783–3793 (1991).

    Article  CAS  Google Scholar 

  26. Ratner, L. et al. AIDS. Res. hum. Retroviruses 3, 57–69 (1987).

    Article  CAS  Google Scholar 

  27. Banker, G. A. & Cowan, W. M. Brain. Res. 126, 397–420 (1977).

    Article  CAS  Google Scholar 

  28. Wilson, M. C. & Higgins, E. A. in Neuromethods: Molecular Neurobiological Techniques Vol. 16 (eds Boulton, A. A., Bake, G. B. & Campagnoni, A. T.) 239–284 (Humana, Clifton, New Jersey, 1989).

    Book  Google Scholar 

  29. Masliah, E. et al. Lab. Invest 66, 285–291 (1992).

    CAS  PubMed  Google Scholar 

  30. Masliah, E. et al. Expl Neurol. 113, 131–142 (1991).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Toggas, S., Masliah, E., Rockenstein, E. et al. Central nervous system damage produced by expression of the HIV-1 coat protein gpl20 in transgenic mice. Nature 367, 188–193 (1994). https://doi.org/10.1038/367188a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/367188a0

  • Springer Nature Limited

This article is cited by

Navigation