尿液糖蛋白图谱揭示了慢性肾脏病的新标记。

International journal of proteomics Pub Date : 2011-01-01 Epub Date: 2011-10-10 DOI:10.1155/2011/214715
Anuradha Vivekanandan-Giri, Jessica L Slocum, Carolyn L Buller, Venkatesha Basrur, Wenjun Ju, Rodica Pop-Busui, David M Lubman, Matthias Kretzler, Subramaniam Pennathur
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引用次数: 0

摘要

慢性肾脏病(CKD)是一个重大的公共卫生问题,进展到终末期肾病会导致发病率和死亡率急剧上升。疾病进展的机制尚不明确,目前的非侵入性标记物与疾病进展的相关性也不完全。因此,亟需发现治疗慢性肾功能衰竭的新型标志物。我们利用糖蛋白组剖析方法来验证一个假设,即慢性肾功能衰竭患者的尿液糖蛋白组剖析将有别于健康对照组。我们从健康对照组和 CKD 患者的尿液中分离并富集了 N-连接的糖蛋白。这一策略确定了 CKD 中多种不同表达的蛋白质,包括具有内肽酶抑制剂活性、蛋白质结合功能和急性期/免疫应激反应活性的多种蛋白质,支持了炎症可能在 CKD 中起核心作用的观点。此外,这些蛋白质中有几个以前曾与肾脏疾病相关,这暗示了它们在疾病发病机制中的作用。总之,我们的观察结果表明,人类尿液糖蛋白组可作为基于机制的新型 CKD 生物标记物的发现源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Urine glycoprotein profile reveals novel markers for chronic kidney disease.

Urine glycoprotein profile reveals novel markers for chronic kidney disease.

Urine glycoprotein profile reveals novel markers for chronic kidney disease.

Urine glycoprotein profile reveals novel markers for chronic kidney disease.

Chronic kidney disease (CKD) is a significant public health problem, and progression to end-stage renal disease leads to dramatic increases in morbidity and mortality. The mechanisms underlying progression of disease are poorly defined, and current noninvasive markers incompletely correlate with disease progression. Therefore, there is a great need for discovering novel markers for CKD. We utilized a glycoproteomic profiling approach to test the hypothesis that the urinary glycoproteome profile from subjects with CKD would be distinct from healthy controls. N-linked glycoproteins were isolated and enriched from the urine of healthy controls and subjects with CKD. This strategy identified several differentially expressed proteins in CKD, including a diverse array of proteins with endopeptidase inhibitor activity, protein binding functions, and acute-phase/immune-stress response activity supporting the proposal that inflammation may play a central role in CKD. Additionally, several of these proteins have been previously linked to kidney disease implicating a mechanistic role in disease pathogenesis. Collectively, our observations suggest that the human urinary glycoproteome may serve as a discovery source for novel mechanism-based biomarkers of CKD.

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