Patschan Susann, Patschan Daniel, Henze Elvira, Blaschke Sabine, Wessels Johannes T, Müller Gerhard Anton
Department of Nephrology and Rheumatology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Int J Nephrol. 2012;2012:715049. doi: 10.1155/2012/715049. Epub 2012 Jun 26.
Background. Granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) are autoimmune-mediated diseases characterized by vasculitic inflammation of respiratory tract and kidneys. Clinical observations indicated a strong association between disease activity and serum levels of certain types of autoantibodies (antineutrophil cytoplasm antibodies with cytoplasmic [cANCA in GPA] or perinuclear [pAN CA in MPA] immunofluorescence). Pathologically, both diseases are characterized by severe microvascular endothelial cell damage. Early endothelial outgrowth cells (eEOCs) have been shown to be critically involved in neovascularization under both physiological and pathological condition. Objectives. The principal aims of our study were (i) to analyze the regenerative activity of the eEOC system and (ii) to determine mPR3 and MPO expression in myelo monocytic cells with endothelial characteristics in GPA and MPA patients. Methods. In 27 GPA and 10 MPA patients, regenerative activity blood-derived eEOCs were analyzed using a culture-forming assay. Flk-1(+), CD133(+)/Flk-1(+), mPR3(+), and Flk-1(+)/mPR3(+) myelomonocytic cells were quantified by FACS analysis. Serum levels of Angiopoietin-1 and TNF-α were measured by ELISA. Results. We found reduced eEOC regeneration, accompanied by lower serum levels of Angiopoietin-1 in GPA patients as compared to healthy controls. In addition, the total numbers of Flk-1(+) myelomonocytic cells in the peripheral circulation were decreased. Membrane PR3 expression was significantly higher in total as well as in Flk-1(+) myelomonocytic cells. Expression of MPO was not different between the groups. Conclusions. These data suggest impairment of the eEOC system and a possible role for PR3 in this process in patients suffering from GPA.
背景。肉芽肿性多血管炎(GPA)和显微镜下多血管炎(MPA)是自身免疫介导的疾病,其特征为呼吸道和肾脏的血管炎性炎症。临床观察表明疾病活动与某些类型自身抗体(在GPA中为胞质抗中性粒细胞胞质抗体[cANCA],在MPA中为核周抗中性粒细胞胞质抗体[pANCA])的血清水平之间存在密切关联。病理上,这两种疾病均以严重的微血管内皮细胞损伤为特征。早期内皮祖细胞(eEOCs)已被证明在生理和病理条件下的新生血管形成中起关键作用。目的。我们研究的主要目的是:(i)分析eEOC系统的再生活性;(ii)确定GPA和MPA患者具有内皮特征的髓单核细胞中mPR3和MPO的表达。方法。对27例GPA患者和10例MPA患者,采用集落形成试验分析血液来源的eEOCs的再生活性。通过流式细胞术分析对Flk-1(+)、CD133(+)/Flk-1(+)、mPR3(+)和Flk-1(+)/mPR3(+)髓单核细胞进行定量。采用酶联免疫吸附测定法检测血清血管生成素-1和肿瘤坏死因子-α水平。结果。我们发现与健康对照相比,GPA患者的eEOC再生减少,同时血清血管生成素-1水平降低。此外,外周循环中Flk-1(+)髓单核细胞的总数减少。膜PR3在总的以及Flk-1(+)髓单核细胞中的表达均显著更高。两组之间MPO的表达无差异。结论。这些数据提示GPA患者的eEOC系统受损,且PR3在此过程中可能发挥作用。