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本文引用的文献

1
Patients with primary membranous nephropathy lack auto-antibodies against LDL receptor, the homologue of megalin in human glomeruli.原发性膜性肾病患者缺乏针对LDL受体(人肾小球中巨膜蛋白的同源物)的自身抗体。
Clin Kidney J. 2012 Apr;5(2):178-179. doi: 10.1093/ndtplus/sfp002. Epub 2012 Jan 31.
2
M-type phospholipase A2 receptor as target antigen in idiopathic membranous nephropathy.M型磷脂酶A2受体作为特发性膜性肾病的靶抗原
N Engl J Med. 2009 Jul 2;361(1):11-21. doi: 10.1056/NEJMoa0810457.
3
Oxidative stress mediates cardiac fibrosis by enhancing transforming growth factor-beta1 in hypertensive rats.氧化应激通过增强高血压大鼠体内的转化生长因子-β1来介导心脏纤维化。
Mol Cell Biochem. 2008 Oct;317(1-2):43-50. doi: 10.1007/s11010-008-9803-8. Epub 2008 Jun 26.
4
Chronic hypoxia aggravates renal injury via suppression of Cu/Zn-SOD: a proteomic analysis.慢性缺氧通过抑制铜锌超氧化物歧化酶加重肾损伤:蛋白质组学分析
Am J Physiol Renal Physiol. 2008 Jan;294(1):F62-72. doi: 10.1152/ajprenal.00113.2007. Epub 2007 Oct 24.
5
Target antigens and nephritogenic antibodies in membranous nephropathy: of rats and men.膜性肾病中的靶抗原和致肾炎抗体:大鼠与人的研究
Semin Immunopathol. 2007 Nov;29(4):445-58. doi: 10.1007/s00281-007-0091-2. Epub 2007 Sep 26.
6
Glomerular clusterin is associated with PKC-alpha/beta regulation and good outcome of membranous glomerulonephritis in humans.肾小球簇集蛋白与蛋白激酶C-α/β调节及人类膜性肾小球肾炎的良好预后相关。
Kidney Int. 2006 Aug;70(3):477-85. doi: 10.1038/sj.ki.5001563. Epub 2006 Jun 14.
7
Developmental expression and function of aldehyde reductase in proximal tubules of the kidney.醛还原酶在肾脏近端小管中的发育表达及功能
Am J Physiol Renal Physiol. 2005 Jul;289(1):F200-7. doi: 10.1152/ajprenal.00411.2004. Epub 2005 Mar 15.
8
Aldose reductase-catalyzed reduction of aldehyde phospholipids.醛糖还原酶催化的醛磷脂还原反应。
J Biol Chem. 2004 Dec 17;279(51):53395-406. doi: 10.1074/jbc.M403416200. Epub 2004 Oct 1.
9
Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathies.MME基因截短突变在母胎同种免疫和产前肾小球病中的作用。
Lancet. 2004;364(9441):1252-9. doi: 10.1016/S0140-6736(04)17142-0.
10
Pathomechanisms and molecular basis of membranous glomerulopathy.膜性肾小球病的发病机制及分子基础
Lancet. 2004;364(9441):1194-6. doi: 10.1016/S0140-6736(04)17154-7.

膜性肾病中的自身免疫反应针对醛糖还原酶和 SOD2。

Autoimmunity in membranous nephropathy targets aldose reductase and SOD2.

机构信息

Division of Nephrology and Laboratory on Pathophysiology of Uremia, G. Gaslini Children Hospital, Genova, Italy.

出版信息

J Am Soc Nephrol. 2010 Mar;21(3):507-19. doi: 10.1681/ASN.2008121259. Epub 2010 Feb 11.

DOI:10.1681/ASN.2008121259
PMID:20150532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2831859/
Abstract

Glomerular targets of autoimmunity in human membranous nephropathy are poorly understood. Here, we used a combined proteomic approach to identify specific antibodies against podocyte proteins in both serum and glomeruli of patients with membranous nephropathy (MN). We detected specific anti-aldose reductase (AR) and anti-manganese superoxide dismutase (SOD2) IgG(4) in sera of patients with MN. We also eluted high titers of anti-AR and anti-SOD2 IgG(4) from microdissected glomeruli of three biopsies of MN kidneys but not from biopsies of other glomerulonephritides characterized by IgG deposition (five lupus nephritis and two membranoproliferative glomerulonephritis). We identified both antigens in MN biopsies but not in other renal pathologies or normal kidney. Confocal and immunoelectron microscopy (IEM) showed co-localization of anti-AR and anti-SOD2 with IgG(4) and C5b-9 in electron-dense podocyte immune deposits. Preliminary in vitro experiments showed an increase of SOD2 expression on podocyte plasma membrane after treatment with hydrogen peroxide. In conclusion, our data support AR and SOD2 as renal antigens of human MN and suggest that oxidative stress may drive glomerular SOD2 expression.

摘要

人类膜性肾病中自身免疫的肾小球靶点知之甚少。在这里,我们使用联合蛋白质组学方法来鉴定膜性肾病患者血清和肾小球中足细胞蛋白的特异性抗体。我们在膜性肾病患者的血清中检测到了特异性的醛糖还原酶 (AR) 和锰超氧化物歧化酶 (SOD2) IgG(4)。我们还从 3 例膜性肾病肾活检中微切割的肾小球洗脱了高滴度的抗 AR 和抗 SOD2 IgG(4),但从其他以 IgG 沉积为特征的肾小球肾炎(5 例狼疮性肾炎和 2 例膜性增生性肾小球肾炎)的活检中没有洗脱。我们在 MN 活检中鉴定了这两种抗原,但在其他肾脏病变或正常肾脏中没有鉴定到。共聚焦和免疫电镜 (IEM) 显示抗 AR 和抗 SOD2 与 IgG(4) 和 C5b-9 在电子致密的足细胞免疫沉积物中共同定位。初步的体外实验表明,用过氧化氢处理后足细胞质膜上 SOD2 的表达增加。总之,我们的数据支持 AR 和 SOD2 作为人类 MN 的肾脏抗原,并表明氧化应激可能驱动肾小球 SOD2 的表达。