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在1型糖尿病患者及其亲属中,zonulin上调与肠道通透性增加有关。

Zonulin upregulation is associated with increased gut permeability in subjects with type 1 diabetes and their relatives.

作者信息

Sapone Anna, de Magistris Laura, Pietzak Michelle, Clemente Maria G, Tripathi Amit, Cucca Francesco, Lampis Rosanna, Kryszak Deborah, Cartenì Maria, Generoso Maddalena, Iafusco Dario, Prisco Francesco, Laghi Francesca, Riegler Gabriele, Carratu Romano, Counts Debra, Fasano Alessio

机构信息

Mucosal Biology Research Center, University of Maryland School of Medicine, 20 Penn Street, Room 345, Baltimore, MD 21201, USA.

出版信息

Diabetes. 2006 May;55(5):1443-9. doi: 10.2337/db05-1593.

Abstract

Zonulin, a protein that modulates intestinal permeability, is upregulated in several autoimmune diseases and is involved in the pathogenesis of autoimmune diabetes in the BB/Wor animal model of the disease. To verify the association between serum zonulin levels and in vivo intestinal permeability in patients with type 1 diabetes, both parameters were investigated in different stages of the autoimmune process. Forty-two percent (141 of 339) of the patients had abnormal serum zonulin levels, as compared with age-matched control subjects. The increased zonulin levels correlated with increased intestinal permeability in vivo and changes in claudin-1, claudin-2, and myosin IXB genes expression, while no changes were detected in ZO1 and occludin genes expression. When tested in serum samples collected during the pre-type 1 diabetes phase, elevated serum zonulin was detected in 70% of subjects and preceded by 3.5 +/- 0.9 years the onset of the disease in those patients who went on to develop type 1 diabetes. Combined, these results suggest that zonulin upregulation is associated with increased intestinal permeability in a subgroup of type 1 diabetic patients. Zonulin upregulation seems to precede the onset of the disease, providing a possible link between increased intestinal permeability, environmental exposure to non-self antigens, and the development of autoimmunity in genetically susceptible individuals.

摘要

闭合蛋白,一种调节肠道通透性的蛋白质,在几种自身免疫性疾病中上调,并参与了该疾病的BB/Wor动物模型中自身免疫性糖尿病的发病机制。为了验证1型糖尿病患者血清闭合蛋白水平与体内肠道通透性之间的关联,在自身免疫过程的不同阶段对这两个参数进行了研究。与年龄匹配的对照受试者相比,42%(339例中的141例)患者的血清闭合蛋白水平异常。闭合蛋白水平升高与体内肠道通透性增加以及紧密连接蛋白-1、紧密连接蛋白-2和肌球蛋白IXB基因表达的变化相关,而在ZO1和闭合蛋白基因表达中未检测到变化。在1型糖尿病前期采集的血清样本中进行检测时,70%的受试者检测到血清闭合蛋白升高,在那些继续发展为1型糖尿病的患者中,该升高比疾病发作提前3.5±0.9年。综合来看,这些结果表明闭合蛋白上调与一部分1型糖尿病患者肠道通透性增加有关。闭合蛋白上调似乎在疾病发作之前出现,这为肠道通透性增加、环境中接触非自身抗原以及遗传易感个体自身免疫的发展之间提供了一个可能的联系。

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