| Literature DB >> 9651362 |
S W Perry1, J A Hamilton, L W Tjoelker, G Dbaibo, K A Dzenko, L G Epstein, Y Hannun, J S Whittaker, S Dewhurst, H A Gelbard.
Abstract
Human immunodeficiency virus type 1 (HIV-1) infection of the central nervous system results in neuronal apoptosis. Activated HIV-1-infected monocytes secrete high levels of the proinflammatory cytokine tumor necrosis factor-alpha (TNF-alpha) and the phospholipid mediator platelet-activating factor (PAF). TNF-alpha and PAF are elevated in the central nervous system of patients with HIV-1-associated dementia. We now demonstrate that conditioned media from activated HIV-1-infected monocytes induces neuronal apoptosis, which can be prevented by co-incubation with PAF acetylhydrolase, the enzyme that catabolizes PAF in the central nervous system. Preceding apoptosis is a TNF-alpha-induced increase in neuronal ceramide levels. TNF-alpha-mediated neuronal apoptosis can also be blocked by co-incubation with PAF acetylhydrolase, or a PAF receptor antagonist. Blocking pathologic activation of PAF receptors may therefore be a pivotal step in the treatment of HIV-1-associated dementia.Entities:
Mesh:
Substances:
Year: 1998 PMID: 9651362 DOI: 10.1074/jbc.273.28.17660
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157