Polentarutti N, Picardi G, Basile A, Cenzuales S, Rivolta A, Matteucci C, Peri G, Mantovani A, Introna M
Department of Immunology and Cell Biology, Istituto di Ricerche Farmacologiche Mario Negri, Milano, Italy.
Eur J Immunol. 1998 Feb;28(2):496-501. doi: 10.1002/(SICI)1521-4141(199802)28:02<496::AID-IMMU496>3.0.CO;2-V.
PTX3 is a prototypic long pentraxin expressed by various cell types, most prominently monocytes and endothelial cells, in response to interleukin-1 (IL-1), tumor necrosis factor (TNF) and bacterial products. In the present report, we show that interferon-gamma (IFN-gamma) inhibits the expression of the PTX3 gene induced by exposure to IL-1, TNF or lipopolysaccharide in human monocytes. This effect is dose dependent and observable when IFN-gamma is added from 24 h before up to 3 h after the addition of IL-1. While the time course of the IL-1-induced PTX3 mRNA expression is not affected, IFN-gamma reduces the stability of the PTX3 mRNA as well as its transcription. The inhibition of PTX3 expression is restricted to monocytes in that no inhibition occurs in cytokine-stimulated fibroblasts and endothelial cells. Under the same conditions, as expected, IFN-gamma augmented monocyte chemotactic protein-1 expression in the same cell preparations. PTX3 protein secretion by activated monocytes is also suppressed by exposure to IFN-gamma. Altogether, these data identify a negative pathway of regulation mediated by IFN-gamma, which may occur under inflammatory conditions.
PTX3是一种典型的长链五聚体蛋白,由多种细胞类型表达,最显著的是单核细胞和内皮细胞,其表达是对白细胞介素-1(IL-1)、肿瘤坏死因子(TNF)和细菌产物的反应。在本报告中,我们表明干扰素-γ(IFN-γ)可抑制人单核细胞暴露于IL-1、TNF或脂多糖后诱导的PTX3基因表达。这种效应具有剂量依赖性,并且当在添加IL-1前24小时至添加IL-1后3小时添加IFN-γ时均可观察到。虽然IL-1诱导的PTX3 mRNA表达的时间进程不受影响,但IFN-γ会降低PTX3 mRNA的稳定性及其转录。PTX3表达的抑制仅限于单核细胞,因为在细胞因子刺激的成纤维细胞和内皮细胞中未发生抑制。在相同条件下,正如预期的那样,IFN-γ会增强同一细胞制剂中单核细胞趋化蛋白-1的表达。暴露于IFN-γ也会抑制活化单核细胞分泌PTX3蛋白。总之,这些数据确定了一种由IFN-γ介导的负调控途径,这种途径可能在炎症条件下发生。