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pubmed-article:11919157pubmed:abstractTextIn HIV-infected patients, production of interleukin-10 (IL-10), a highly immunosuppressive cytokine, is associated with the disease progression toward AIDS. We have previously shown that HIV-1 Tat induces IL-10 production by human monocytes via a protein kinase C (PKC) -dependent pathway. Here we show that PKC activation by Tat is essential for IL-10 induction. Among the eight PKC isoforms present in human monocytes, we investigated which isoform(s) plays this crucial role in Tat-mediated IL-10 production and show that 1) Tat can activate PKC-alpha, PKC-betaII, PKC-delta, and PKC-epsilon, 2) of these four potential candidates, only PKC-betaII, PKC-delta, and PKC-epsilon are activated by the active domain Tat 1-45, which is responsible for IL-10 production and depleted by long-term exposure to PMA, which abolishes Tat-mediated IL-10 production, 3) whereas selective inhibition of PKC-alpha and PKC-epsilon by specific antisense oligonucleotides has no effect on Tat-mediated IL-10 induction, inhibition of either PKC-betaII or PKC-delta partially inhibits IL-10 production; and 4) the simultaneous inhibition of PKC-betaII and PKC-delta totally inhibits Tat-mediated IL-10. Altogether, these results suggest that the induction of IL-10 by Tat is strictly dependent on the PKC-delta and -betaII isoforms.lld:pubmed
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pubmed-article:11919157pubmed:pagination546-54lld:pubmed
pubmed-article:11919157pubmed:dateRevised2009-11-19lld:pubmed
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pubmed-article:11919157pubmed:articleTitleHIV-1 Tat protein induces interleukin-10 in human peripheral blood monocytes: involvement of protein kinase C-betaII and -delta.lld:pubmed
pubmed-article:11919157pubmed:affiliationLaboratoire d'Immuno-Virologie, EA 3038, Université Paul Sabatier, 31062 Toulouse, France.lld:pubmed
pubmed-article:11919157pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11919157pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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