Pendergraft W F, Alcorta D A, Segelmark M, Yang J J, Tuttle R, Jennette J C, Falk R J, Preston G A
Division of Nephrology and Hypertension, Department of Medicine, University of North Carolina at Chapel Hill, 27599, USA.
Kidney Int. 2000 May;57(5):1981-90. doi: 10.1046/j.1523-1755.2000.00048.x.
One hypothesis for the pathogenesis of vasculitis associated with antineutrophil cytoplasmic autoantibodies (ANCAs) proposes that ANCAs bind to ANCA antigens, such as proteinase 3 (PR3) or myeloperoxidase (MPO), which are produced by endothelial cells and expressed on their surfaces. There are conflicting reports, however, on whether endothelial cells express the ANCA antigen PR3, and there are no reports on endothelial expression of MPO. The aim of this study was to determine the presence or absence of PR3 and MPO mRNA in both venous and arterial endothelial cells, employing standard reverse transcription-polymerase chain reaction (RT-PCR) techniques and also the quantitative and highly specific method, TaqMan PCR.
RT-PCR (with 3 primer sets) and TaqMan PCR, a method for detecting low copy transcripts, were used to probe for PR3 and MPO transcripts in human endothelial cells from umbilical vein (HUVEC) and artery (HUAEC) and from lung microvascular (HLMVEC). Cells were treated with interferon-gamma (200 units/mL) or tumor necrosis factor-alpha (3 or 10 ng/mL) or both.
Transcripts for PR3 and/or MPO were not detected in HUVEC, HUAEC, and HLMVEC by standard RT-PCR. Analyses for PR3 protein confirmed that PR3 is not expressed in HUVEC. HUVEC and HUAEC were negative for PR3 and MPO by TaqMan PCR.
PR3 and MPO are not expressed in HUVEC, HUAEC, or HLMVEC. Endothelial cell presentation of endogenous PR3 and MPO antigens is not involved in the pathogenesis of ANCA-associated vasculitis. Alternative explanations need to be explored to determine the pathogenic effect of ANCAs.
抗中性粒细胞胞浆自身抗体(ANCA)相关血管炎发病机制的一种假说是,ANCA与蛋白酶3(PR3)或髓过氧化物酶(MPO)等ANCA抗原结合,这些抗原由内皮细胞产生并表达于其表面。然而,关于内皮细胞是否表达ANCA抗原PR3的报道存在矛盾,且尚无关于内皮细胞表达MPO的报道。本研究的目的是采用标准逆转录-聚合酶链反应(RT-PCR)技术以及定量且高度特异的TaqMan PCR方法,确定静脉和动脉内皮细胞中PR3和MPO mRNA的有无。
RT-PCR(使用3对引物)和用于检测低拷贝转录本的TaqMan PCR,用于检测来自脐静脉(HUVEC)、动脉(HUAEC)和肺微血管(HLMVEC)的人内皮细胞中的PR3和MPO转录本。细胞用γ干扰素(200单位/毫升)或肿瘤坏死因子-α(3或10纳克/毫升)或两者进行处理。
通过标准RT-PCR在HUVEC、HUAEC和HLMVEC中未检测到PR3和/或MPO的转录本。对PR3蛋白的分析证实PR3在HUVEC中不表达。通过TaqMan PCR检测,HUVEC和HUAEC中PR3和MPO均为阴性。
PR3和MPO在HUVEC、HUAEC或HLMVEC中不表达。内源性PR3和MPO抗原的内皮细胞呈递不参与ANCA相关血管炎的发病机制。需要探索其他解释来确定ANCA的致病作用。