Sairenji T, Ohnishi E, Inouye S, Kurata T
Department of Biosignaling, School of Life Science, Faculty of Medicine, Tottori University, Yonago, Japan.
Viral Immunol. 1998;11(4):221-31. doi: 10.1089/vim.1998.11.221.
Human (h) interleukin-10 (IL-10) exhibits a strong DNA and amino acid sequence homology to the Epstein-Barr virus (EBV) BCRF1 genome, viral (v) IL-10. We analyzed the production of IL-10 for EBV activation in B-cell lines. The latent EBV in Akata cells was activated by the cross-linking of surface immunoglobulin G (IgG) with anti-human IgG. The levels of IL-10(h+v) and vIL-10 in the culture fluids were measured by a specific enzyme-linked immunosorbent assay (ELISA). IL-10(h+v) was detected at the same time for EBV immediate early gene BZLF1 product ZEBRA and early gene BMRF1 product EA-D. This was more than 4 hours prior to the appearance of vIL-10, and late gene products gp 350/220 and viral capsid antigen. The induction of hIL-10 and vIL-10 mRNAs were detected in anti-IgG-treated Akata cells by reverse transcription-polymerase chain reaction. The induction of IL-10(h+v) and vIL-10 was inhibited with a tyrosine kinase inhibitor, herbimycin, or with an inhibitor of herpesvirus DNA polymerase, phosphonoacetic acid, or acyclovir. IL-10(h+v) and vIL-10 were also detected in the supernatants of Akata and Daudi but not Ramos cells infected with P3HR-1 EBV. These results show the IL-10 induction on EBV activation in EBV-carrying B-cell lines.
人(h)白细胞介素-10(IL-10)与爱泼斯坦-巴尔病毒(EBV)的BCRF1基因组即病毒(v)IL-10在DNA和氨基酸序列上具有高度同源性。我们分析了B细胞系中EBV激活时IL-10的产生情况。用抗人IgG交联表面免疫球蛋白G(IgG)可激活Akata细胞中的潜伏EBV。通过特异性酶联免疫吸附测定(ELISA)检测培养液中IL-10(h + v)和vIL-10的水平。在检测到EBV即刻早期基因BZLF1产物ZEBRA和早期基因BMRF1产物EA-D的同时检测到了IL-10(h + v)。这比vIL-10以及晚期基因产物gp 350/220和病毒衣壳抗原出现的时间早4个多小时。通过逆转录-聚合酶链反应在抗IgG处理的Akata细胞中检测到了hIL-10和vIL-10 mRNA的诱导。酪氨酸激酶抑制剂赫伯霉素、疱疹病毒DNA聚合酶抑制剂膦甲酸或阿昔洛韦可抑制IL-10(h + v)和vIL-10的诱导。在感染P3HR-1 EBV的Akata和Daudi细胞的上清液中也检测到了IL-10(h + v)和vIL-10,但在Ramos细胞中未检测到。这些结果表明在携带EBV的B细胞系中EBV激活可诱导IL-10产生。