Eder Katalin, Guan Hongtao, Sung Hye Y, Ward Jon, Angyal Adrienn, Janas Michelle, Sarmay Gabriella, Duda Erno, Turner Martin, Dower Steven K, Francis Sheila E, Crossman David C, Kiss-Toth Endre
Cardiovascular Research Unit, University of Sheffield, Sheffield, UK.
Int Immunol. 2008 Dec;20(12):1543-50. doi: 10.1093/intimm/dxn116. Epub 2008 Oct 24.
Inflammatory activation of monocytes is an essential part of both innate immune responses and the pathogenesis of conditions such as atherosclerosis. However, the mechanisms which modulate the response of monocytes to inflammatory stimuli are still poorly understood. Here, we report that tribbles-2 (trb-2) is a novel regulator of inflammatory activation of monocytes. Down-regulation of trb-2 levels potentiates LPS-induced IL-8 production via enhanced activation of the extracellular signal-regulated kinase and jun kinase mitogen-activated protein kinase (MAPK) pathways. In keeping with this, the endogenous level of trb-2 expression in human primary monocytes is inversely correlated to the cell's ability to produce IL-8. We show that trb-2 is a binding partner and a negative regulator of selected MAPKs. The potential in vivo relevance of these findings is highlighted by the observation that modified low-density lipoprotein profoundly down-regulates trb-2 expression, which may, in turn, significantly contribute to the inflammatory processes in the development of vascular disease. Taken together, our results define trb-2 as a potent novel regulator of monocyte biology, controlling the activation of these cells.
单核细胞的炎症激活是先天性免疫反应和动脉粥样硬化等疾病发病机制的重要组成部分。然而,调节单核细胞对炎症刺激反应的机制仍知之甚少。在此,我们报告tribbles-2(trb-2)是单核细胞炎症激活的一种新型调节因子。trb-2水平的下调通过增强细胞外信号调节激酶和Jun激酶丝裂原活化蛋白激酶(MAPK)途径的激活来增强脂多糖诱导的白细胞介素-8(IL-8)产生。与此一致的是,人原代单核细胞中trb-2表达的内源性水平与细胞产生IL-8的能力呈负相关。我们表明,trb-2是特定MAPK的结合伙伴和负调节因子。修饰的低密度脂蛋白显著下调trb-2表达这一观察结果突出了这些发现的潜在体内相关性,这反过来可能对血管疾病发展中的炎症过程有显著贡献。综上所述,我们的结果将trb-2定义为单核细胞生物学的一种强效新型调节因子,控制这些细胞的激活。