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Recombinant human immunodeficiency virus type-1 (HIV-1) Tat protein sequentially up-regulates IL-6 and TGF-beta 1 mRNA expression and protein synthesis in peripheral blood monocytes.
Gibellini D; Zauli G; Re MC; Milani D; Furlini G; Caramelli E; Capitani
April 30, 1995
Br J Haematol. 1994 Oct;88(2):261-7. Unique Identifier : AIDSLINE

In this study we evaluated the effect of human immunodeficiency virus type 1 (HIV-1) recombinant Tat protein on mRNA expression and protein synthesis of two inflammatory cytokines-interleukin-6 (IL-6) and transforming growth factor-beta 1 (TGF-beta 1)-by peripheral blood (PB) monocytes. Whereas maximal levels of IL-6 protein were recovered in PB monocyte culture supernatants after 24-48 h from the addition of 1 micrograms/ml of recombinant Tat, TGF-beta 1 showed a slower and progressive increase, reaching maximal levels only after 72-96 h of culture. Consistently, the analysis of the steady-state levels of mRNA showed a sharp increase of IL-6 mRNA expression after 24h of culture, with a slow decline thereafter. On the other hand, TGF-beta 1 mRNA expression showed a slow increase only after 72-96 h of culture. Moreover, IL-6 appeared involved in the up-regulation of TGF-beta 1, because the addition of a neutralizing anti-IL-6 antibody to Tat-treated PB monocyte cultures significantly reduced the amounts of TGF-beta 1 recovered in the culture supernatants after 96 h. The present demonstration that HIV-1 Tat protein directly up-regulates IL-6 expression and stimulates TGF-beta 1 production both directly and indirectly, through early IL-6 production, could have important implications in the pathogenesis of HIV-1 disease.

Blotting, Northern Cells, Cultured Gene Products, tat/*PHARMACOLOGY Human *HIV-1 Interleukin-6/*BIOSYNTHESIS/GENETICS Kinetics Monocytes/*DRUG EFFECTS/METABOLISM Recombinant Proteins/PHARMACOLOGY RNA, Messenger/GENETICS Support, Non-U.S. Gov't Transforming Growth Factor beta/*BIOSYNTHESIS/GENETICS Up-Regulation (Physiology)/DRUG EFFECTS JOURNAL ARTICLE