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内皮细胞和肾上皮细胞不表达韦格纳自身抗原——蛋白酶3。

Endothelial cells and renal epithelial cells do not express the Wegener's autoantigen, proteinase 3.

作者信息

King W J, Adu D, Daha M R, Brooks C J, Radford D J, Pall A A, Savage C O

机构信息

Department of Medicine, CCRIS, Medical School, Birmingham University, Edgbaston, UK.

出版信息

Clin Exp Immunol. 1995 Oct;102(1):98-105. doi: 10.1111/j.1365-2249.1995.tb06642.x.

Abstract

Proteinase 3 (PR3) is the major antigen for autoantibodies (C-ANCA) against cytoplasmic components of neutrophils which are strongly associated with Wegener's granulomatosis (WG). Recent data that PR3 may be expressed by renal tubular epithelial cells and endothelial cells suggest potential for a direct pathogenic effect against these cells by C-ANCA or cytoxic T lymphocytes. Using a semi-quantitative polymerase chain reaction (PCR), ELISA and indirect immunofluorescence staining we studied endothelial and epithelial cell PR3 expression. By PCR, no PR3 expression was found in human umbilical vein endothelial cells (HUVEC) either untreated, or when treated with interferon-gamma (IFN-gamma) (200 U/ml, 6 h, 24 h), IL-1 (20 U/ml, 6 h), tumour necrosis factor-alpha, (TNF-alpha) (200 U/ml, 0, 1, 2, 4, 6 h) or IFN-gamma + TNF-alpha (6 h); iliac vein and artery endothelial cells did not express PR3 either. In contrast, PR3 was detected in HL60 cells and neutrophils by PCR, expression being confirmed by sequence analysis. Three PR3 MoAbs showed no binding to unstimulated or TNF-alpha-stimulated HUVEC either by ELISA or by indirect immunofluorescence staining. The epithelial cell line A549 expressed PR3 when assayed by PCR. However, three renal epithelial cell lines (two tubular and one glomerular) showed little or no PR3 expression by PCR or ELISA. These studies fail to demonstrate evidence for PR3 expression by endothelial cells, even when using the highly sensitive PCR assay. Whilst PR3 expression by A549 cells is intriguing, the relevance of this in the pathology of WG is doubtful considering the negligible expression by renal epithelial cell lines.

摘要

蛋白酶3(PR3)是抗中性粒细胞胞质成分自身抗体(C-ANCA)的主要抗原,这些自身抗体与韦格纳肉芽肿病(WG)密切相关。最近有数据表明,PR3可能由肾小管上皮细胞和内皮细胞表达,这提示C-ANCA或细胞毒性T淋巴细胞可能对这些细胞产生直接致病作用。我们采用半定量聚合酶链反应(PCR)、酶联免疫吸附测定(ELISA)和间接免疫荧光染色法,研究了内皮细胞和上皮细胞中PR3的表达情况。通过PCR检测发现,人脐静脉内皮细胞(HUVEC)无论是未处理的,还是用γ干扰素(IFN-γ)(200 U/ml,6小时,24小时)、白细胞介素-1(IL-1)(20 U/ml,6小时)、肿瘤坏死因子-α(TNF-α)(200 U/ml,0、1、2、4、6小时)或IFN-γ + TNF-α(6小时)处理后,均未表达PR3;髂静脉和动脉内皮细胞也未表达PR3。相比之下,通过PCR在HL60细胞和中性粒细胞中检测到了PR3,序列分析证实了其表达。三种PR3单克隆抗体通过ELISA或间接免疫荧光染色,均未显示与未刺激或TNF-α刺激的HUVEC有结合。通过PCR检测,上皮细胞系A549表达PR3。然而,三种肾上皮细胞系(两种肾小管细胞系和一种肾小球细胞系)通过PCR或ELISA检测,几乎未表达或未表达PR3。这些研究未能证明内皮细胞表达PR3的证据,即使使用高灵敏度的PCR检测方法也是如此。虽然A549细胞表达PR3很有趣,但考虑到肾上皮细胞系的表达可忽略不计,这在WG病理学中的相关性值得怀疑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/948c/1553320/697f71786434/clinexpimmunol00217-0108-a.jpg

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