Wang S Keisin, Xie Jie, Green Linden A, McCready Robert A, Motaganahalli Raghu L, Fajardo Andres, Babbey Clifford C, Murphy Michael P
Indiana University School of Medicine, Richard Roudebush Veteran Affairs Medical Center, Department of Surgery, Division of Vascular Surgery and Center for Aortic Disease, Indianapolis, Indiana.
Indiana University School of Medicine, Richard Roudebush Veteran Affairs Medical Center, Department of Surgery, Division of Vascular Surgery and Center for Aortic Disease, Indianapolis, Indiana.
J Surg Res. 2017 Dec;220:311-319. doi: 10.1016/j.jss.2017.06.078. Epub 2017 Aug 12.
The formation of abdominal aortic aneurysms (AAA) is characterized by a dominance of proinflammatory forces that result in smooth muscle cell apoptosis, extracellular matrix degradation, and progressive diameter expansion. Additional defects in the antiinflammatory response may also play a role but have yet to be fully characterized. TSG-6 (TNF-stimulated gene-6) is a potent antiinflammatory protein involved in extracellular matrix stabilization and cell migration active in many pathological conditions. Here, we describe its role in AAA formation.
Blood and/or aortic tissue samples were collected from organ donors, subjects undergoing elective AAA screening, and open surgical AAA repair. Aortic specimens collected were preserved for IHC or immediately assayed after tissue homogenization. Protein concentrations in tissue and plasma were assayed by ELISA. All immune cell populations were assayed using FACS. In vitro, macrophage polarization from monocytes was performed with young, healthy donor PBMCs.
TSG-6 was found to be abnormally elevated in both the plasma and aortic wall of patients with AAA compared with healthy and risk-factor matched non-AAA donors. We observed the highest tissue concentration of TSG-6 in the less-diseased proximal and distal shoulders compared with the central aspect of the aneurysm. IHC localized most TSG-6 to the tunica media with minor expression in the tunica adventitia of the aortic wall. Higher concentrations of both M1 and M2 macrophages where also observed, however M1/M2 ratios were unchanged from healthy controls. We observed no difference in M1/M2 ratios in the peripheral blood of risk-factor matched non-AAA and AAA patients. Interesting, TSG-6 inhibited the polarization of the antiinflammatory M2 phenotype in vitro.
AAA formation results from an imbalance of inflammatory forces causing aortic wall infiltration of mononuclear cells leading to the vessel breakdown. In the AAA condition, we report an elevation of TSG-6 expression in both the aortic wall and the peripheral circulation.
腹主动脉瘤(AAA)的形成以促炎力量占主导为特征,这会导致平滑肌细胞凋亡、细胞外基质降解以及瘤体直径逐渐增大。抗炎反应中的其他缺陷可能也起作用,但尚未完全明确。TSG-6(肿瘤坏死因子刺激基因-6)是一种强效抗炎蛋白,参与细胞外基质稳定和细胞迁移,在多种病理状况下发挥作用。在此,我们描述其在AAA形成中的作用。
从器官捐献者、接受择期AAA筛查的受试者以及AAA开放手术修复患者中采集血液和/或主动脉组织样本。采集的主动脉标本保存用于免疫组化(IHC),或在组织匀浆后立即进行检测。通过酶联免疫吸附测定(ELISA)检测组织和血浆中的蛋白浓度。使用荧光激活细胞分选术(FACS)检测所有免疫细胞群体。在体外,用年轻健康供者的外周血单核细胞(PBMC)诱导单核细胞向巨噬细胞极化。
与健康和有风险因素匹配的非AAA捐献者相比,发现AAA患者的血浆和主动脉壁中TSG-6异常升高。我们观察到,与动脉瘤中心部位相比,病变较轻的近端和远端肩部TSG-6的组织浓度最高。免疫组化显示,大多数TSG-6定位于主动脉壁的中膜,在外膜有少量表达。还观察到M1和M2巨噬细胞浓度均较高,然而M1/M2比值与健康对照无变化。我们发现有风险因素匹配的非AAA和AAA患者外周血中的M1/M2比值无差异。有趣的是,TSG-6在体外抑制抗炎M2表型的极化。
AAA的形成是由于炎症力量失衡导致单核细胞浸润主动脉壁,进而导致血管破裂。在AAA情况下,我们报告主动脉壁和外周循环中TSG-6表达均升高。