Brigino E, Haraguchi S, Koutsonikolis A, Cianciolo G J, Owens U, Good R A, Day N K
Department of Pediatrics, University of South Florida, St. Petersburg 33701, USA.
Proc Natl Acad Sci U S A. 1997 Apr 1;94(7):3178-82. doi: 10.1073/pnas.94.7.3178.
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 gamma 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.
HIV-1 Nef蛋白与免疫抑制且高度保守的逆转录病毒跨膜蛋白p15E具有显著同源性。在本研究中,细胞外Nef蛋白可诱导人外周血单个核细胞以及H9 T和U937人原单核细胞系细胞中白细胞介素(IL)-10 mRNA的表达。Nef刺激外周血单个核细胞后,IL-10蛋白释放到上清液中的过程呈剂量依赖性。细胞因子IL-2、IL-4、IL-5、IL-12 p40、IL-13和干扰素γ的表达不受Nef刺激的影响。Nef诱导的IL-10蛋白产生受到钙/钙调蛋白磷酸二酯酶抑制剂W-7的抑制,但不受蛋白激酶A抑制剂H-89以及蛋白激酶C抑制剂星形孢菌素和钙磷蛋白C的抑制。钙螯合剂EGTA也抑制Nef诱导的IL-10产生,并且通过同时添加钙和Nef可逆转这种抑制作用。这些发现表明,细胞外Nef可能通过诱导IL-10而在HIV感染的免疫发病机制中发挥作用。