Deng Jingti, James Christian H, Patel Lisa, Smith Alberto, Burnand Kevin G, Rahmoune Hassan, Lamb Jonathan R, Davis Bill
GlaxoSmithKline Clinical Unit, Addenbrooke's Centre for Clinical Investigation, Addenbrooke's Hospital, Cambridge CB2 2GG, U.K.
Clin Sci (Lond). 2009 Feb;116(3):241-8. doi: 10.1042/CS20080058.
Mammalian orthologues of the Drosophila tribbles protein (Trb1, Trb2 and Trb3) are a recently described family of signalling molecules that regulate gene expression by modulation of protein kinase signalling pathways. In the present study, a screen for mRNA species specifically regulated in vulnerable regions of human atherosclerotic plaque demonstrated the up-regulation of both Trb1 and Trb2, the latter by more than 8-fold. In vitro experiments in primary human monocyte-derived macrophages showed that Trb2 expression was up-regulated by treatment with oxidized LDL (low-density lipoprotein), and that expression of recombinant Trb2 specifically reduced macrophage levels of IL-10 (interleukin-10) mRNA. Our results thus identify Trb2 as a highly regulated gene in vulnerable atherosclerotic lesions, and demonstrate inhibition of macrophage IL-10 biosynthesis as a potential pro-inflammatory consequence of high Trb2 expression, which may contribute to plaque instability.
果蝇类三磷酸肌醇结合蛋白(Trb1、Trb2和Trb3)的哺乳动物直系同源物是最近描述的一类信号分子家族,它们通过调节蛋白激酶信号通路来调控基因表达。在本研究中,一项针对人类动脉粥样硬化斑块易损区域特异性调控的mRNA种类的筛选显示,Trb1和Trb2均上调,后者上调超过8倍。原代人单核细胞衍生巨噬细胞的体外实验表明,氧化型低密度脂蛋白(LDL)处理可上调Trb2表达,并且重组Trb2的表达特异性降低了巨噬细胞中白细胞介素-10(IL-10)mRNA的水平。因此,我们的结果确定Trb2是易损动脉粥样硬化病变中一个高度受调控的基因,并证明抑制巨噬细胞IL-10生物合成是Trb2高表达的潜在促炎后果,这可能导致斑块不稳定。