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成人T细胞白血病细胞中白细胞介素8的产生:人T细胞白血病病毒I型tax可能对白细胞介素8基因进行反式激活。

Production of interleukin 8 in adult T-cell leukemia cells: possible transactivation of the interleukin 8 gene by human T-cell leukemia virus type I tax.

作者信息

Mori N, Murakami S, Oda S, Prager D, Eto S

机构信息

First Department of Internal Medicine, University of Occupational and Environmental Health, School of Medicine, Kitakyushu, Japan.

出版信息

Cancer Res. 1995 Aug 15;55(16):3592-7.

PMID:7627968
Abstract

Interleukin 8 (IL-8) mRNA was detected in peripheral leukemic cells obtained from adult T-cell leukemia patients, as well as in cultured human T-cell leukemia virus type I (HTLV-I)-infected T-cell lines (HUT-102, MT-1, SALT-3, and SKT-1B). With the use of ELISA, IL-8 protein was also detected in the culture medium of these cells and in the extracellular fluids of patients. Furthermore, we demonstrated that the HTLV-I-derived transactivator protein, tax, could stimulate endogenous IL-8 gene expression in an uninfected T-cell line (Jurkat) and in a rheumatoid synovial cell line (E-11). Induction of IL-8 by tax at protein level was also demonstrated in transfected cells. We found that the IL-8 NF-kappa B-binding site specifically formed a complex with NF-kappa B-containing nuclear extracts from HTLV-I-infected T-cell lines and freshly isolated leukemic cells from adult T-cell leukemia patients. Finally, transfection of HTLV-I tax into Jurkat cells resulted in induction of specific binding of nuclear extracts to the NF-kappa B sequence. These results suggest that the HTLV-I tax gene may transactivate the IL-8 gene through the kappa B site in HTLV-I-infected cells and that constitutive expression of the IL-8 gene may play a role in HTLV-I-associated pathogenesis.

摘要

在从成人T细胞白血病患者获取的外周白血病细胞中检测到白细胞介素8(IL-8)信使核糖核酸(mRNA),在培养的人I型T细胞白血病病毒(HTLV-I)感染的T细胞系(HUT-102、MT-1、SALT-3和SKT-1B)中也检测到该信使核糖核酸。使用酶联免疫吸附测定(ELISA)法,在这些细胞的培养基以及患者的细胞外液中也检测到了IL-8蛋白。此外,我们证明HTLV-I衍生的反式激活蛋白tax可刺激未感染的T细胞系(Jurkat)和类风湿性滑膜细胞系(E-11)中的内源性IL-8基因表达。在转染细胞中也证实了tax在蛋白水平上诱导IL-8的产生。我们发现IL-8核因子κB(NF-κB)结合位点与来自HTLV-I感染的T细胞系以及从成人T细胞白血病患者新鲜分离的白血病细胞中含NF-κB的核提取物特异性形成复合物。最后,将HTLV-I tax转染到Jurkat细胞中导致核提取物与NF-κB序列的特异性结合增加。这些结果表明,HTLV-I tax基因可能通过HTLV-I感染细胞中的κB位点反式激活IL-8基因,并且IL-8基因的组成型表达可能在HTLV-I相关的发病机制中起作用。

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