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人淋巴细胞和单核细胞系中核褪黑素受体表达与细胞因子产生增强之间的相关性。

Correlation between nuclear melatonin receptor expression and enhanced cytokine production in human lymphocytic and monocytic cell lines.

作者信息

García-Mauriño S, Pozo D, Calvo J R, Guerrero J M

机构信息

Department of Medical Biochemistry and Molecular Biology, The University of Seville School of Medicine and Virgen Macarena Hospital, Spain.

出版信息

J Pineal Res. 2000 Oct;29(3):129-37. doi: 10.1034/j.1600-079x.2000.290301.x.

Abstract

The report shows that melatonin enhances IL-2 and IL-6 production by two human lymphocytic (Jurkat) and monocytic (U937) cell lines via a nuclear receptor-mediated mechanism. Jurkat cells express nuclear (RZRalpha, RORalpha1 and RORalpha2) and membrane (mt1) melatonin receptors, and melatonin binds to Jurkat nuclei and membranes with the same affinity described for human peripheral blood mononuclear cells (PBMCs). Melatonin enhances IL-2 production by Jurkat cells activated by either phytohemagglutinin (PHA) or phorbol myristate acetate (PMA). PHA activation of Jurkat cells does not change the profile of melatonin receptor expression; on the contrary, PMA activation negatively regulates the mtl receptor. In the absence of the membrane receptor, melatonin still activates IL-2 production. U937 cells express only the mtl receptor. Although melatonin binds to both U937 nuclei and membranes, CGP 52608, a ligand of the nuclear receptor for melatonin, does not inhibit melatonin binding to U937 nuclei, suggesting that a protein other than the RZR/RORalpha receptor was involved in the process. In U937 cells, melatonin did not modify basal production of IL-6 or when activated by PMA plus LPS (lipopolysaccharide), a treatment that downregulates the expression of the mtl receptor. However, in U937 cells activated with IFN-gamma, which induces the expression of the RORgamma1 and RORalpha2 nuclear receptors and represses the expression of the mt1 receptor, melatonin can activate IL-6 production. These results show that the expression of nuclear melatonin receptor is sufficient for melatonin to activate cytokine production in human lymphocytic and monocytic cell lines.

摘要

该报告显示,褪黑素通过核受体介导的机制增强了两种人类淋巴细胞(Jurkat)和单核细胞(U937)细胞系中IL-2和IL-6的产生。Jurkat细胞表达核(RZRα、RORα1和RORα2)和膜(mt1)褪黑素受体,并且褪黑素以与人类外周血单核细胞(PBMC)相同的亲和力与Jurkat细胞核和膜结合。褪黑素增强了由植物血凝素(PHA)或佛波酯(PMA)激活的Jurkat细胞中IL-2的产生。Jurkat细胞的PHA激活不会改变褪黑素受体表达的概况;相反,PMA激活会负向调节mtl受体。在没有膜受体的情况下,褪黑素仍能激活IL-2的产生。U937细胞仅表达mtl受体。尽管褪黑素与U937细胞核和膜都结合,但CGP 52608,一种褪黑素核受体的配体,并不抑制褪黑素与U937细胞核的结合,这表明除RZR/RORα受体之外的一种蛋白质参与了该过程。在U937细胞中,褪黑素不会改变IL-6的基础产生,也不会改变由PMA加脂多糖(LPS)激活时IL-6的产生,PMA加LPS的处理会下调mtl受体的表达。然而,在用干扰素-γ激活的U937细胞中,干扰素-γ诱导RORγ1和RORα2核受体的表达并抑制mt1受体的表达,褪黑素可以激活IL-6的产生。这些结果表明,核褪黑素受体的表达足以使褪黑素激活人类淋巴细胞和单核细胞系中细胞因子的产生。

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