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糖皮质激素抗炎作用的分子机制

Molecular mechanisms of anti-inflammatory action of glucocorticoids.

作者信息

Cato A C, Wade E

机构信息

Forschungszentrum Karlsruhe, Institute of Genetics, Germany.

出版信息

Bioessays. 1996 May;18(5):371-8. doi: 10.1002/bies.950180507.

Abstract

Glucocorticoid hormones are effective in controlling inflammation, but the mechanisms that confer this action are largely unknown. Recent advances in this field have shown that both positive and negative regulation of gene expression are necessary for this process. The genes whose activity are modulated in the anti-inflammatory process code for several cytokines, adhesion molecules and enzymes. Most of them do not carry a classical binding site for regulation by a glucocorticoid receptor, but have instead regulatory sequences for transcription factors such as AP-1 or NF-kappa B. This makes them unusual targets for glucocorticoid action and emphasizes the need for novel regulatory mechanisms. Recent studies describe an important contribution by protein-protein interactions, in which several domains of the receptor participate; these studies provide a better understanding of the action of the receptor and offer opportunities for the design of steroidal compounds that could function more effectively as anti-inflammatory drugs.

摘要

糖皮质激素在控制炎症方面很有效,但赋予这种作用的机制在很大程度上尚不清楚。该领域的最新进展表明,基因表达的正调控和负调控对于这个过程都是必需的。在抗炎过程中其活性受到调节的基因编码几种细胞因子、黏附分子和酶。它们中的大多数没有糖皮质激素受体调节的经典结合位点,而是具有转录因子如AP-1或核因子κB的调控序列。这使得它们成为糖皮质激素作用的特殊靶点并强调了新型调控机制的必要性。最近的研究描述了蛋白质-蛋白质相互作用的重要贡献,其中受体的几个结构域参与其中;这些研究能更好地理解受体的作用,并为设计能更有效地发挥抗炎药物作用的甾体化合物提供了机会。

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