Suppr超能文献

炎性细胞因子可诱导人视网膜色素上皮细胞培养物合成细胞间黏附分子-1(ICAM-1)mRNA并分泌其蛋白。

Inflammatory cytokines induce intercellular adhesion molecule-1 (ICAM-1) mRNA synthesis and protein secretion by human retinal pigment epithelial cell cultures.

作者信息

Nagineni C N, Kutty R K, Detrick B, Hooks J J

机构信息

Immunology & Virology Section, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Cytokine. 1996 Aug;8(8):622-30. doi: 10.1006/cyto.1996.0083.

Abstract

Retinal inflammatory diseases in man are associated with an upregulation in the expression of intercellular adhesion molecule-1 (ICAM-1) in cells within the retina and with an increase in soluble ICAM-1 within the vitreous. These studies suggest that this protein may contribute to immunopathological processes within the eye. The effects of inflammatory mediators on the regulation of the expression and secretion of ICAM-1 by human retinal pigment epithelial cell cultures (HRPE) were investigated in order to identify the possible source of soluble ICAM-1 and the conditions which enhance its production. Immunofluorescence studies on TNF-alpha and/or IFN-gamma treated HRPE cells demonstrated cellular expression of ICAM-1 which was predominantly localized to intercellular junctions. Moreover, treatment of HRPE for 24 h with tumour necrosis factor alpha (TNF-alpha) (10 ng/ml), interferon gamma (IFN-gamma) (500 u/ml), interleukin 1 alpha (IL-1 alpha) (10 ng/ml) and IL-1 beta (10 ng/ml) results in the secretion of ICAM-1, ranging from 9 to 13 ng per 10(6) cells. IFN-gamma acts synergistically with (TNF-alpha) and IL-1 in the secretion of ICAM-1 by HRPE. Only 1.75 ng of soluble ICAM-1 was detected in untreated HRPE cells. In contrast, lipopolysaccharide (LPS), IL-6, IFN-alpha or TGF-beta did not exhibit any influence on ICAM-1 secretion by these cells. Northern blot analysis reveals an increased expression of ICAM-1 mRNA in HRPE stimulated with IFN-gamma, TNF-alpha or IL-1 for 24 h. In untreated cells, ICAM-1 mRNA is not detectable. There is a progressive increase in ICAM-1 mRNA levels in cytokine-treated HRPE, that reaches steady state by 12 h. Furthermore, a close correlation is noted between ICAM-1 mRNA levels and the secretion of ICAM-1 protein, suggesting regulation at the level of gene transcription. ICAM-1 secretion by RPE might actively participate in the immune reactions in the retina, by recruiting and activating lymphocytes, and contribute to the immunopathological processes in inflammatory diseases.

摘要

人类视网膜炎症性疾病与视网膜内细胞间黏附分子 -1(ICAM -1)表达上调以及玻璃体内可溶性 ICAM -1 增加有关。这些研究表明,这种蛋白质可能参与眼部的免疫病理过程。为了确定可溶性 ICAM -1 的可能来源以及增强其产生的条件,研究了炎症介质对人视网膜色素上皮细胞培养物(HRPE)中 ICAM -1 表达和分泌的调节作用。对经肿瘤坏死因子 -α(TNF -α)和 / 或干扰素 -γ(IFN -γ)处理的 HRPE 细胞进行免疫荧光研究,结果显示 ICAM -1 的细胞表达主要定位于细胞间连接。此外,用肿瘤坏死因子 -α(TNF -α)(10 ng/ml)、干扰素 -γ(IFN -γ)(500 u/ml)、白细胞介素 -1α(IL -1α)(10 ng/ml)和白细胞介素 -1β(IL -1β)(10 ng/ml)处理 HRPE 24 小时后,会导致 ICAM -1 的分泌,每 10⁶ 个细胞分泌量在 9 到 13 ng 之间。IFN -γ 与 TNF -α 和 IL -1 在 HRPE 分泌 ICAM -1 方面具有协同作用。在未处理的 HRPE 细胞中仅检测到 1.75 ng 的可溶性 ICAM -1。相比之下,脂多糖(LPS)、IL -6、IFN -α 或转化生长因子 -β(TGF -β)对这些细胞的 ICAM -1 分泌没有任何影响。Northern 印迹分析显示,经 IFN -γ、TNF -α 或 IL -1 刺激 24 小时的 HRPE 中 ICAM -1 mRNA 的表达增加。在未处理的细胞中,无法检测到 ICAM -1 mRNA。细胞因子处理的 HRPE 中 ICAM -1 mRNA 水平逐渐升高,在 12 小时时达到稳定状态。此外,注意到 ICAM -1 mRNA 水平与 ICAM -1 蛋白分泌之间存在密切相关性,这表明在基因转录水平上存在调节。RPE 分泌的 ICAM -1 可能通过募集和激活淋巴细胞,积极参与视网膜中的免疫反应,并促成炎症性疾病中的免疫病理过程。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验