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IgA肾病与扁桃体、血清及肾小球IgA1的异常糖基化

IgA nephropathy and aberrant glycosylation of tonsillar, serum and glomerular IgA1.

作者信息

Hiki Yoshiyuki, Ito Akihiko, Yamamoto Yoshihiro, Yamamoto Koichiro, Iwase Hitoo

机构信息

School of Health Sciences and Medicine, Fujita Health University, Aichi, Japan.

出版信息

Adv Otorhinolaryngol. 2011;72:68-70. doi: 10.1159/000324609. Epub 2011 Aug 18.

DOI:10.1159/000324609
PMID:21865693
Abstract

Human IgA1, which is the predominant subtype deposited in the glomeruli in IgA nephropathy (IgAN), has a unique mucin-like structure in its hinge region. Several studies suggested that the IgA1 molecules in IgAN patients had an aberrant structure of O-glycans. The paper summarizes the analyses of O-glycan structure in the IgA1 molecules taken from tonsils, sera and glomeruli of patients with IgAN. Hypoglycosylation, especially hypogalactosylation of O-glycans has been observed not only in serum and glomerular IgA1 but also in tonsillar IgA1.

摘要

人类IgA1是IgA肾病(IgAN)中沉积于肾小球的主要亚型,其铰链区具有独特的黏蛋白样结构。多项研究表明,IgAN患者的IgA1分子具有异常的O-聚糖结构。本文总结了对取自IgAN患者扁桃体、血清和肾小球的IgA1分子中O-聚糖结构的分析。不仅在血清和肾小球IgA1中,而且在扁桃体IgA1中都观察到了O-聚糖的低糖化,尤其是低半乳糖基化。

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IgA nephropathy and aberrant glycosylation of tonsillar, serum and glomerular IgA1.IgA肾病与扁桃体、血清及肾小球IgA1的异常糖基化
Adv Otorhinolaryngol. 2011;72:68-70. doi: 10.1159/000324609. Epub 2011 Aug 18.
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