Date Published:
2007
Publication Type:
Journal Article
Authors:
Secondary:
The FASEB Journal: Official Publication of the Federation of American Societies for Experimental Biology
Volume:
21
Pagination:
777-89
URL:
https://pubmed.ncbi.nlm.nih.gov/
Keywords:
Astrocytes;Brain;Cell Cycle Proteins;Endothelin-1;External;Gene Expression Regulation;Gene Products;HIV Infections;HIV-1;Humans;Interleukin-6;Interleukin-8;Messenger;Neoplastic;NF-kappa B;Promoter Regions (Genetics);RNA;tat;tat Gene Prod
Abstract:
<p>Human Immune Deficiency Virus-1 (HIV-1) infection can induce severe and debilitating neurological problems, including behavioral abnormalities, motor dysfunction, and dementia. HIV can persistently infect astrocytes, during which viral accessory proteins are produced that are unaffected by current antiretroviral therapy. The effect of these proteins on astrocyte function remains unknown. Astrocytes are the predominant cells within the brain; thus, disruption of astrocyte function could influence the neuropathogenesis of HIV infection. To explore further these effects, we constitutively expressed HIV-Tat protein in astrocytes. Since the nuclear presence of Tat protein leads to alteration of host gene expression, we further analyzed the effects of Tat on host gene transcripts. Endothelin-1 (ET-1) was a significantly elevated transcript as verified by reverse transcription-polymerase chain reaction (RT-PCR), and it was subsequently released extracellularly in Tat-expressing and HIV-infected astrocytes. ET-1 expression was also prominent in reactive astrocytes and neurons in brain tissues from basal ganglia and frontal lobes of HIV encephalitic patients. HIV-Tat regulated ET-1 at the transcriptional level through NF-kappaB (NF-kappaB)-responsive sites in the ET-1 promoter. Intriguingly, simvastatin (10 microM) down-regulated HIV-Tat-induced ET-1 and also inhibited activation of NF-kappaB in astrocytes. Our findings suggest that ET-1 may be critical in mediating the neuropathogenesis of HIV dementia and that statins may have therapeutic potential in these patients.</p>