Interleukin 10 is Induced by Recombinant HIV-1 Nef Protein Involving the Calcium/Calmodulin-Dependent Phosphodiesterase Signal Transduction Pathway

HIV-1 Nef protein shares a significant homology with the immunosuppressive and highly conserved retroviral transmembrane protein p15E. In the present study, extracellular Nef protein is shown to induce interleukin (IL)-10 mRNA expression in human peripheral blood mononuclear cells as well as in cell...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 94; no. 7; pp. 3178 - 3182
Main Authors Brigino, Emerita, Haraguchi, Soichi, Koutsonikolis, Angelos, Cianciolo, George J., Owens, Una, Good, Robert A., Day, Noorbibi K.
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences of the United States of America 01.04.1997
National Acad Sciences
National Academy of Sciences
The National Academy of Sciences of the USA
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Summary:HIV-1 Nef protein shares a significant homology with the immunosuppressive and highly conserved retroviral transmembrane protein p15E. In the present study, extracellular Nef protein is shown to induce interleukin (IL)-10 mRNA expression in human peripheral blood mononuclear cells as well as in cells of H9 T and U937 promonocytic human cell lines. Release of IL-10 protein into supernatants of peripheral blood mononuclear cells stimulated with Nef is dose-dependent. Expression of cytokines IL-2, IL-4, IL-5, IL-12 p40, IL-13, and interferon γ is not affected by Nef stimulation. IL-10 protein production induced by Nef is inhibited by the calcium/calmodulin phosphodiesterase inhibitor W-7 but not by the protein kinase A inhibitor H-89 nor the protein kinase C inhibitors staurosporine and calphostin C. The calcium chelating agent EGTA also inhibits the IL-10 production induced by Nef, and this inhibition is reversed by the addition of calcium along with Nef. These findings indicate that extracellular Nef may contribute to the immunopathogenesis of HIV infection by inducing IL-10.
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To whom reprint requests should be addressed at: Department of Pediatrics, All Children’s Hospital, 801 Sixth Street South, St. Petersburg, FL 33701.
Robert A. Good
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.94.7.3178