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KMID : 0357319970320020245
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Journal of the Korean Society for Microbiology
1997 Volume.32 No. 2 p.245 ~ p.254
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Effect of HIV-1 Gp41 Peptide on Expression and Metabolism of Amyloid Precursor Protein in Human Astroglioma Cell
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Abstract
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Significant neurodegeneration leading to neurocognitive disorder and dementia has been observed in the central nervous system (CNS) of patients with HIV infection. Part of the neurodegenerative cascade in AIDS dementia may involve glial cells,
perhaps
through inhibiting the release of glial factors that protect neurons from variety of insults. Here, in an effort to find the mediators of HIV-induced brain damage, we examined the possible effect of a HIV-1 transmenbrane protein gp41 peptide
(583-599)
on expression and metabolism of amyloid precursor protein (APP) using human astroglial cell line. RT-PCR analysis demonstrated that gp 41 peptide did not significantly change expression patterns of APP mRNAs in lipopolysaccharide (LPS) activated
astroglial cells for 6h. In contrast, gp41 peptide remarkably downregulated the level of secreted from of APP (sAPPa), which has been recently demonstrated as a potent neuroprotective factor. The reverse peptide, used as control had no such
effect.
The
mechanism of gp41 peptide-induced down regulation of sAPPa production appears to be TGF-βindependent. These results implicate that gp41 peptide could be one of the mediator involved in the modulation of APP secretion within CNS, possibly
contributing
to the neuronal degeneration in HIV-1 associated neurological disease.
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