Suppr超能文献

白细胞介素(IL)-10可抑制大鼠腹膜肥大细胞长期产生IL-6,但不抑制其预先形成的介质释放。

Interleukin (IL)-10 inhibits long-term IL-6 production but not preformed mediator release from rat peritoneal mast cells.

作者信息

Marshall J S, Leal-Berumen I, Nielsen L, Glibetic M, Jordana M

机构信息

Intestinal Disease Research Programme, McMaster University, Health Science Centre, Hamilton, Ontario, Canada.

出版信息

J Clin Invest. 1996 Feb 15;97(4):1122-8. doi: 10.1172/JCI118506.

Abstract

Mast cells have been implicated in a number of diseases involving chronic inflammation including asthma, rheumatoid arthritis, and inflammatory bowel diseases. They are a potent source of several cytokines, including IL-6 and TNF-alpha. Freshly isolated rat peritoneal mast cells will produce IL-6 in response to anti-IgE, LPS, PGE1, or PGE2; however, the mechanisms by which such cytokine production is regulated are poorly understood. IL-10 is recognized as an important immunoregulatory cytokine with effects on T cell development and the production of inflammatory cytokines. IL-10 has previously been described to enhance mast cell development in the context of IL-3 and IL-4. In the current study, we have examined the ability of IL-10 to modulate rat peritoneal mast cell IL-6 and TNF-alpha production in response to a variety of stimuli. We have observed that recombinant murine IL-10 can inhibit the production of both IL-6 and TNF-alpha by mast cells without altering the degree of histamine release in response to anti-IgE. Concentrations of IL-10 as low as 0.2 ng/ml were sufficient to inhibit IL-6 production by LPS- or anti-IgE-activated cells significantly. IL-10 also inhibited PGE1- and PGE2-induced IL-6 production. The relative potency of IL-10 as an inhibitor of mast cell IL-6 production was highly dependent upon the stimulus used, with a 10-fold difference in the IC50 for LPS- or anti-IgE-activated cells (0.21 ng/ml) and cells activated with a combination of LPS and PGE2 (2.29 ng/ml). This suggests that prostanoids may limit the ability of IL-10 to modulate mast cell IL-6 production in the context of inflammation. These data have important implications for the regulation of mast cell IL-6 in inflammatory diseases involving prostanoid production and the effects of treatment with cyclooxygenase inhibitors. Our results also demonstrate a dual role for IL-10 on mast cells as a growth factor and inhibitor of cytokine production.

摘要

肥大细胞与包括哮喘、类风湿性关节炎和炎症性肠病在内的多种慢性炎症性疾病有关。它们是多种细胞因子的重要来源,包括白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)。新鲜分离的大鼠腹膜肥大细胞会因抗IgE、脂多糖(LPS)、前列腺素E1(PGE1)或前列腺素E2(PGE2)而产生IL-6;然而,这种细胞因子产生的调节机制尚不清楚。白细胞介素-10(IL-10)被认为是一种重要的免疫调节细胞因子,对T细胞发育和炎症细胞因子的产生有影响。此前曾描述过IL-10在白细胞介素-3(IL-3)和白细胞介素-4(IL-4)的背景下可促进肥大细胞发育。在本研究中,我们检测了IL-10调节大鼠腹膜肥大细胞对多种刺激产生IL-6和TNF-α的能力。我们观察到重组小鼠IL-10可抑制肥大细胞产生IL-6和TNF-α,而不改变其对抗IgE的组胺释放程度。低至0.2 ng/ml的IL-10浓度就足以显著抑制LPS或抗IgE激活的细胞产生IL-6。IL-10也抑制PGE1和PGE2诱导的IL-6产生。IL-10作为肥大细胞IL-6产生抑制剂的相对效力高度依赖于所使用的刺激物,LPS或抗IgE激活的细胞(0.21 ng/ml)与LPS和PGE2联合激活的细胞(2.29 ng/ml)的半数抑制浓度(IC50)相差10倍。这表明前列腺素可能会限制IL-10在炎症背景下调节肥大细胞IL-6产生的能力。这些数据对于涉及前列腺素产生的炎症性疾病中肥大细胞IL-6的调节以及环氧化酶抑制剂治疗的效果具有重要意义。我们的结果还证明了IL-10在肥大细胞上作为生长因子和细胞因子产生抑制剂的双重作用。

相似文献

引用本文的文献

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验