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蛋白质组学分析有助于更好地了解乳糜泻:重点关注表位识别和自身抗体。

Proteomic analyses lead to a better understanding of celiac disease: focus on epitope recognition and autoantibodies.

机构信息

Experimental and Clinical Pharmacology Unit, Molecular Oncology and Translational Medicine, Domert, Centro di Riferimento Oncologico, IRCCS National Cancer Institute, via F. Gallini 2, Aviano, PN, Italy.

出版信息

Dig Dis Sci. 2010 Nov;55(11):3041-6. doi: 10.1007/s10620-010-1323-1. Epub 2010 Jul 15.

DOI:10.1007/s10620-010-1323-1
PMID:20632103
Abstract

Proteomic technologies are being used with increasing frequency in the scientific community. In this review, we have highlighted their use in celiac disease (CD). The available techniques, which include two-dimensional (2D) gel electrophoresis, mass spectrometry, and antibody and tissue arrays, have been used to identify proteins or changes in protein expression specific to gut tissue from patients with CD. A number of studies have employed proteomic methodologies to determine the diagnostic biomarkers in body fluids or to examine changes in protein expression and posttranslational modifications during signaling. A fast technological development of these methods, along with the combination of classic techniques with proteomics, will lead to new discoveries, which will consent a better understanding of the pathogenesis of CD.

摘要

蛋白质组学技术在科学界中的应用越来越频繁。在这篇综述中,我们强调了它们在乳糜泻(CD)中的应用。现有的技术包括二维(2D)凝胶电泳、质谱和抗体及组织阵列,这些技术被用于鉴定来自 CD 患者肠道组织的特异性蛋白或蛋白表达变化。许多研究采用蛋白质组学方法来确定体液中的诊断生物标志物,或检查信号转导过程中蛋白表达和翻译后修饰的变化。这些方法的快速技术发展,以及经典技术与蛋白质组学的结合,将带来新的发现,这将有助于更好地理解 CD 的发病机制。

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Proteomic analyses lead to a better understanding of celiac disease: focus on epitope recognition and autoantibodies.蛋白质组学分析有助于更好地了解乳糜泻:重点关注表位识别和自身抗体。
Dig Dis Sci. 2010 Nov;55(11):3041-6. doi: 10.1007/s10620-010-1323-1. Epub 2010 Jul 15.
2
Epitope mapping of the N-terminal portion of tissue transglutaminase protein antigen to identify linear epitopes in celiac disease.组织转谷氨酰胺酶蛋白抗原N端部分的表位作图,以鉴定乳糜泻中的线性表位。
J Pept Sci. 2014 Sep;20(9):689-95. doi: 10.1002/psc.2650. Epub 2014 May 15.
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Antibodies to human tissue transglutaminase for the diagnosis of celiac disease.用于诊断乳糜泻的抗人组织转谷氨酰胺酶抗体。
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引用本文的文献

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The Screening of Critical Related Genes in Celiac Disease Based on Intraepithelial Lymphocytes Investigation: A Bioinformatics Analysis.基于上皮内淋巴细胞研究的乳糜泻关键相关基因筛选:一项生物信息学分析
Galen Med J. 2019 Aug 14;8:e1407. doi: 10.31661/gmj.v8i0.1407. eCollection 2019.
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Protein-protein interaction network of celiac disease.乳糜泻的蛋白质-蛋白质相互作用网络。
Gastroenterol Hepatol Bed Bench. 2016 Fall;9(4):268-277.
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Overexpression of Hsp70 confers cytoprotection during gliadin exposure in Caco-2 cells.热休克蛋白70(Hsp70)的过表达在麦醇溶蛋白暴露期间赋予Caco-2细胞细胞保护作用。

本文引用的文献

1
Do gliadin and tissue transglutaminase mediate PPAR downregulation in intestinal cells of patients with coeliac disease?麦醇溶蛋白和组织转谷氨酰胺酶是否介导乳糜泻患者肠道细胞中过氧化物酶体增殖物激活受体(PPAR)的下调?
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PPAR signaling pathway and cancer-related proteins are involved in celiac disease-associated tissue damage.过氧化物酶体增殖物激活受体(PPAR)信号通路及癌症相关蛋白参与了乳糜泻相关的组织损伤。
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麦醇溶蛋白 p31-43 肽在肠上皮细胞和乳糜泻黏膜中的溶酶体积累诱导氧化应激和组织转谷氨酰胺酶介导的过氧化物酶体增殖物激活受体 γ 下调。
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Galectin-10, eosinophils, and celiac disease.半乳糖凝集素-10、嗜酸性粒细胞与乳糜泻
Ann N Y Acad Sci. 2009 Sep;1173:357-64. doi: 10.1111/j.1749-6632.2009.04627.x.
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The metabonomic signature of celiac disease.乳糜泻的代谢组学特征。
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6
A new HLA-A*680106 allele identified in individuals with celiac disease from the Friuli area of northeast Italy.在意大利东北部弗留利地区患有乳糜泻的个体中鉴定出一种新的HLA - A*680106等位基因。
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7
Secretion of celiac disease autoantibodies after in vitro gliadin challenge is dependent on small-bowel mucosal transglutaminase 2-specific IgA deposits.体外麦醇溶蛋白激发后乳糜泻自身抗体的分泌取决于小肠黏膜转谷氨酰胺酶2特异性IgA沉积。
BMC Immunol. 2008 Feb 29;9:6. doi: 10.1186/1471-2172-9-6.
8
Mechanisms of epithelial translocation of the alpha(2)-gliadin-33mer in coeliac sprue.乳糜泻中α(2)-麦醇溶蛋白-33聚体的上皮转运机制
Gut. 2008 Jun;57(6):747-54. doi: 10.1136/gut.2007.136366. Epub 2008 Feb 27.
9
Mass spectrometry analysis of gliadins in celiac disease.乳糜泻中醇溶蛋白的质谱分析
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10
Associated autoantibodies in celiac disease.乳糜泻相关的自身抗体。
Autoimmun Rev. 2007 Sep;6(8):559-65. doi: 10.1016/j.autrev.2007.02.006. Epub 2007 Mar 6.