Thacker Seth G, Berthier Celine C, Mattinzoli Deborah, Rastaldi Maria Pia, Kretzler Matthias, Kaplan Mariana J
Division of Rheumatology, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
J Immunol. 2010 Oct 1;185(7):4457-69. doi: 10.4049/jimmunol.1001782. Epub 2010 Aug 30.
Systemic lupus erythematosus (SLE) is characterized by increased vascular risk due to premature atherosclerosis independent of traditional risk factors. We previously proposed that IFN-α plays a crucial role in premature vascular damage in SLE. IFN-α alters the balance between endothelial cell apoptosis and vascular repair mediated by endothelial progenitor cells (EPCs) and myeloid circulating angiogenic cells (CACs). In this study, we demonstrate that IFN-α promotes an antiangiogenic signature in SLE and control EPCs/CACs, characterized by transcriptional repression of IL-1α and β, IL-1R1, and vascular endothelial growth factor A, and upregulation of IL-1R antagonist and the decoy receptor IL-1R2. IL-1β promotes significant improvement in the functional capacity of lupus EPCs/CACs, therefore abrogating the deleterious effects of IFN-α. The beneficial effects from IL-1 are mediated, at least in part, by increases in EPC/CAC proliferation, by decreases in EPC/CAC apoptosis, and by preventing the skewing of CACs toward nonangiogenic pathways. IFN-α induces STAT2 and 6 phosphorylation in EPCs/CACs, and JAK inhibition abrogates the transcriptional antiangiogenic changes induced by IFN-α in these cells. Immunohistochemistry of renal biopsies from patients with lupus nephritis, but not anti-neutrophil cytoplasmic Ab-positive vasculitis, showed this pathway to be operational in vivo, with increased IL-1R antagonist, downregulation of vascular endothelial growth factor A, and glomerular and blood vessel decreased capillary density, compared with controls. Our study introduces a novel putative pathway by which type I IFNs may interfere with vascular repair in SLE through repression of IL-1-dependent pathways. This could promote atherosclerosis and loss of renal function in this disease.
系统性红斑狼疮(SLE)的特征是由于早发性动脉粥样硬化导致血管风险增加,且这种情况与传统风险因素无关。我们之前提出,干扰素-α(IFN-α)在SLE的早发性血管损伤中起关键作用。IFN-α改变了内皮细胞凋亡与由内皮祖细胞(EPC)和髓系循环血管生成细胞(CAC)介导的血管修复之间的平衡。在本研究中,我们证明IFN-α在SLE及对照EPC/CAC中促进抗血管生成特征,其特点是白细胞介素-1α和β(IL-1α和β)、IL-1受体1(IL-1R1)以及血管内皮生长因子A(VEGF-A)的转录抑制,以及IL-1受体拮抗剂和诱饵受体IL-1R2的上调。IL-1β显著改善狼疮EPC/CAC的功能能力,从而消除IFN-α的有害作用。IL-1的有益作用至少部分是通过EPC/CAC增殖增加、EPC/CAC凋亡减少以及防止CAC向非血管生成途径的偏移来介导的。IFN-α诱导EPC/CAC中的信号转导和转录激活因子2(STAT2)和6磷酸化,而抑制Janus激酶(JAK)可消除IFN-α在这些细胞中诱导的转录性抗血管生成变化。狼疮性肾炎患者而非抗中性粒细胞胞浆抗体阳性血管炎患者的肾活检免疫组织化学显示,与对照组相比,该途径在体内起作用,表现为IL-1受体拮抗剂增加、血管内皮生长因子A下调以及肾小球和血管的毛细血管密度降低。我们的研究引入了一条新的假定途径,通过该途径I型干扰素可能通过抑制IL-依赖性途径干扰SLE中的血管修复。这可能会促进该疾病中的动脉粥样硬化和肾功能丧失。