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热休克蛋白70在细胞因子产生中的作用。

Role of hsp70 in cytokine production.

作者信息

Hall T J

机构信息

Ciba Geigy Ltd, Research Department, Basel, Switzerland.

出版信息

Experientia. 1994 Nov 30;50(11-12):1048-53. doi: 10.1007/BF01923460.

Abstract

Interleukin-1 and tumor necrosis factor-alpha are potent, multifunctional cytokine mediators of inflammation and immune responses that are produced primarily by activated monocytes and macrophages. Three published papers by different groups have shown that heat shock and chemical stress with heavy metal salts or sulfhydryl reagents, all of which induce the expression of heat shock protein 70 (hsp70), concomitantly inhibit the production of these cytokines in human monocytes and mouse macrophages activated by lipopolysaccharide. These papers are reviewed and discussed in some detail. Other studies suggest that various anti-inflammatory drugs, including acetylsalicyclic acid, auranofin and dexamethasone, can also facilitate HSP expression in macrophages. However, while these studies are interesting, it is clear that not a great deal of work has been done and/or published in this area. Since many pharmaceutical companies are developing cytokine synthesis inhibitors as potential anti-inflammatory drugs, one aim of this article is to emphasize that understanding the molecular mechanism(s) that lead to increased HSP expression and decreased cytokine biosynthesis may assist in achieving this goal.

摘要

白细胞介素 -1 和肿瘤坏死因子 -α 是炎症和免疫反应中强大的多功能细胞因子介质,主要由活化的单核细胞和巨噬细胞产生。不同研究小组发表的三篇论文表明,热休克以及用重金属盐或巯基试剂进行化学应激,所有这些都会诱导热休克蛋白 70(hsp70)的表达,同时抑制脂多糖激活的人单核细胞和小鼠巨噬细胞中这些细胞因子的产生。本文将对这些论文进行较为详细的综述和讨论。其他研究表明,包括乙酰水杨酸、金诺芬和地塞米松在内的各种抗炎药物,也可以促进巨噬细胞中热休克蛋白的表达。然而,尽管这些研究很有趣,但很明显在这个领域尚未开展大量工作和/或发表大量成果。由于许多制药公司正在开发细胞因子合成抑制剂作为潜在的抗炎药物,本文的一个目的是强调,了解导致热休克蛋白表达增加和细胞因子生物合成减少的分子机制可能有助于实现这一目标。

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