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白细胞介素1和肿瘤坏死因子-α协同增加人滑膜成纤维细胞中白细胞介素6的产生。

Interleukin 1 and tumor necrosis factor-alpha synergistically increase the production of interleukin 6 in human synovial fibroblast.

作者信息

Harigai M, Hara M, Kitani A, Norioka K, Hirose T, Hirose W, Suzuki K, Kawakami M, Masuda K, Shinmei M

机构信息

First Department of Medicine, National Defense Medical College, Saitama, Japan.

出版信息

J Clin Lab Immunol. 1991 Mar;34(3):107-13.

PMID:1667942
Abstract

We have previously reported that synovial cells could participate in B cell differentiation processes in rheumatoid arthritis (RA) by producing interleukin-6 (IL-6) spontaneously or in response to interleukin-1 (IL-1) stimulation. In this paper, we examined the effects of tumor necrosis factor-alpha (TNF-alpha) on IL-6 production by human synovial fibroblasts. TNF-alpha, as well as IL-1, is a putative relevant molecule in the inflammatory process and in articular destruction in RA. Both IL-1 and TNF-alpha induced IL-6 production by synovial fibroblasts in a dose dependent manner. When synovial fibroblasts were stimulated by IL-1 and TNF-alpha in combination, IL-6 production increased synergistically after 48 hr of a 72 hr culture period. Kinetic studies revealed that the presence of both cytokines at the early phase of stimulation was required for the synergistic effect. These results suggest that TNF-alpha could be involved in a cytokine network in the affected joints of RA and could contribute synergistically with IL-1 to the IL-6 production by synovial fibroblasts in vivo.

摘要

我们之前曾报道,滑膜细胞可通过自发产生白细胞介素-6(IL-6)或响应白细胞介素-1(IL-1)刺激参与类风湿关节炎(RA)中的B细胞分化过程。在本文中,我们研究了肿瘤坏死因子-α(TNF-α)对人滑膜成纤维细胞产生IL-6的影响。TNF-α以及IL-1是RA炎症过程和关节破坏中一种公认的相关分子。IL-1和TNF-α均以剂量依赖性方式诱导滑膜成纤维细胞产生IL-6。当滑膜成纤维细胞受到IL-1和TNF-α联合刺激时,在72小时培养期的48小时后,IL-6产生协同增加。动力学研究表明,刺激早期两种细胞因子的存在是协同效应所必需的。这些结果表明,TNF-α可能参与RA受累关节中的细胞因子网络,并可能在体内与IL-1协同促进滑膜成纤维细胞产生IL-6。

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