Cedars-Sinai Medical Center, Davis Bldg. 1016, 8700 Beverly Blvd., Los Angeles, CA 90048, USA.
FASEB J. 2010 Mar;24(3):810-22. doi: 10.1096/fj.09-140780. Epub 2009 Nov 16.
Neovascularization is critical to destabilization of atheroma. We previously reported that the angiogenic growth factor pleiotrophin (PTN) coaxes monocytes to assume the phenotype of functional endothelial cells in vitro and in vivo. In this study we show that PTN expression is colocalized with capillaries of human atherosclerotic plaques. Among the various reagents that are critical to the pathogenesis of atherosclerosis, interferon (IFN)-gamma was found to markedly induce PTN mRNA expression in a dose-dependent manner in macrophages. Mechanistic studies revealed that the Janus kinase inhibitors, WHI-P154 and ATA, efficiently blocked STAT1 phosphorylation in a concentration- and time-dependent manner. Notably, the level of phosphorylated STAT1 was found to correlate directly with the PTN mRNA levels. In addition, STAT1/STAT3/p44/42 signaling molecules were found to be phosphorylated by IFN-gamma in macrophages, and they were translocated into the nucleus. Further, PTN promoter analysis showed that a gamma-activated sequence (GAS) located at -2086 to -2078 bp is essential for IFN-gamma-regulated promoter activity. Moreover, electrophoretic mobility shift, supershift, and chromatin immunoprecipitation analyses revealed that both STAT1 and STAT3 bind to the GAS at the chromatin level in the IFN-gamma stimulated cells. Finally, to test whether the combined effect of STAT1/STAT3/p44/42 signaling is required for the expression of PTN in macrophages, gene knockdowns of these transcription factors were performed using siRNA. Cells lacking STAT1, but not STAT3 or p42, have markedly reduced PTN mRNA levels. These data suggest that PTN expression in the human plaques may be in part regulated by IFN-gamma and that PTN is involved in the adaptive immunity.-Li, F., Tian, F., Wang, L., Williamson, I. K., Sharifi, B. G., Shah, P. K. Pleiotrophin (PTN) is expressed in vascularized human atherosclerotic plaques: IFN-gamma/JAK/STAT1 signaling is critical for the expression of PTN in macrophages.
血管新生对于动脉粥样硬化的不稳定至关重要。我们之前的研究报告表明,血管生成生长因子多效蛋白(PTN)可以诱使单核细胞在体外和体内表现出功能性内皮细胞的表型。在这项研究中,我们发现 PTN 的表达与人类动脉粥样硬化斑块的毛细血管共定位。在对动脉粥样硬化发病机制至关重要的各种试剂中,干扰素(IFN)-γ被发现以剂量依赖的方式显著诱导巨噬细胞中 PTN mRNA 的表达。机制研究表明,Janus 激酶抑制剂 WHI-P154 和 ATA 能够以浓度和时间依赖的方式有效阻断 STAT1 的磷酸化。值得注意的是,磷酸化 STAT1 的水平与 PTN mRNA 水平直接相关。此外,IFN-γ刺激巨噬细胞中发现 STAT1/STAT3/p44/42 信号分子发生磷酸化,并被转位到细胞核内。此外,PTN 启动子分析表明,位于-2086 至-2078bp 的 γ 激活序列(GAS)对于 IFN-γ调节的启动子活性是必需的。此外,电泳迁移率变动、超迁移和染色质免疫沉淀分析显示,在 IFN-γ刺激的细胞中,STAT1 和 STAT3 均在染色质水平上与 GAS 结合。最后,为了测试 STAT1/STAT3/p44/42 信号的组合效应是否是巨噬细胞中 PTN 表达所必需的,使用 siRNA 对这些转录因子进行基因敲低。缺乏 STAT1 的细胞,但不缺乏 STAT3 或 p42,PTN mRNA 水平明显降低。这些数据表明,人类斑块中的 PTN 表达可能部分受到 IFN-γ的调节,并且 PTN 参与适应性免疫。-李芳、田芳、王琳、威廉姆森、沙里菲、沙阿。多效蛋白(PTN)在血管化的人类动脉粥样硬化斑块中表达:IFN-γ/JAK/STAT1 信号对于巨噬细胞中 PTN 的表达至关重要。