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非造血细胞中的CD40功能。核因子κB的激活及白细胞介素-6生成的诱导。

CD40 function in nonhematopoietic cells. Nuclear factor kappa B mobilization and induction of IL-6 production.

作者信息

Hess S, Rensing-Ehl A, Schwabe R, Bufler P, Engelmann H

机构信息

Institute for Immunology, University of Munich, Germany.

出版信息

J Immunol. 1995 Nov 15;155(10):4588-95.

PMID:7594457
Abstract

CD40 is a member of the TNF receptor family that was first characterized as an important T-B cell interaction molecule. This receptor is also expressed on many other cell types, including normal basal epithelium, carcinomas, and transformed cell lines. The functions of CD40 in non-B cells are largely unknown. Our studies demonstrate that CD40 mediates nuclear factor kappa B (NF-kappa B) mobilization and IL-6 production in nonhematopoietic cells. Stimulation of the transformed fibroblast cell line SV80 with CD40 ligand (CD40L) or anti-CD40 Ab resulted in the production of IL-6; this could be increased by IFN-gamma pretreatment, which is known to up-regulate CD40 expression. Studies with transfectants overexpressing CD40 demonstrated that activation of CD40 alone is sufficient to induce IL-6 production. The transcription factor NF-kappa B appears to play a central role in CD40-mediated activation of the IL-6 gene; NF-kappa B mobilization directly preceded CD40-mediated IL-6 production, and suppression of NF-kappa B mobilization with the metabolic inhibitor D609 also suppressed the IL-6 response. A striking similarity to the requirements for TNF-induced IL-6 production, which is mediated by the p55TNF receptor in SV80 cells, was observed. In view of the intracellular homologies between CD40 and the p55TNF receptor, it should be considered that the two receptors share common components in their signaling pathways that lead to IL-6 production.

摘要

CD40是肿瘤坏死因子受体家族的成员,最初被鉴定为一种重要的T细胞与B细胞相互作用分子。该受体也在许多其他细胞类型中表达,包括正常基底上皮细胞、癌细胞和转化细胞系。CD40在非B细胞中的功能大多未知。我们的研究表明,CD40在非造血细胞中介导核因子κB(NF-κB)的激活和白细胞介素-6(IL-6)的产生。用CD40配体(CD40L)或抗CD40抗体刺激转化的成纤维细胞系SV80可导致IL-6的产生;已知干扰素-γ预处理可上调CD40表达,从而增加IL-6的产生。对过表达CD40的转染子的研究表明,单独激活CD40足以诱导IL-6的产生。转录因子NF-κB似乎在CD40介导的IL-6基因激活中起核心作用;NF-κB的激活直接先于CD40介导的IL-6产生,用代谢抑制剂D609抑制NF-κB的激活也抑制了IL-6反应。观察到与SV80细胞中由p55肿瘤坏死因子受体介导的肿瘤坏死因子诱导的IL-6产生的需求有显著相似性。鉴于CD40与p55肿瘤坏死因子受体之间的细胞内同源性,应该认为这两种受体在导致IL-6产生的信号通路中共享共同成分。

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