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干扰素-γ下调大鼠肠道和人Caco-2/bbe细胞中Na(+)/H(+)交换体NHE2和NHE3的表达。

IFN-gamma downregulates expression of Na(+)/H(+) exchangers NHE2 and NHE3 in rat intestine and human Caco-2/bbe cells.

作者信息

Rocha F, Musch M W, Lishanskiy L, Bookstein C, Sugi K, Xie Y, Chang E B

机构信息

The Martin Boyer Laboratories, University of Chicago, Chicago, Illinois 60637, USA.

出版信息

Am J Physiol Cell Physiol. 2001 May;280(5):C1224-32. doi: 10.1152/ajpcell.2001.280.5.C1224.

Abstract

Diarrhea associated with inflammatory bowel diseases has traditionally been attributed to stimulated secretion. The purpose of this study was to determine whether chronic stimulation of intestinal mucosa by interferon-gamma (IFN-gamma) affects expression and function of the apical membrane Na(+)/H(+) exchangers NHE2 and NHE3 in rat intestine and Caco-2/bbe (C2) cells. Confluent C2 cells expressing NHE2 and NHE3 were treated with IFN-gamma for 2, 24, and 48 h. Adult rats were injected with IFN-gamma intraperitoneally for 12 and 48 h. NHE2 and NHE3 activities were measured by unidirectional (22)Na influx across C2 cells and in rat brush-border membrane vesicles. NHE protein and mRNA were assessed by Western and Northern blotting. IFN-gamma treatment of C2 monolayers caused a >50% reduction in NHE2 and NHE3 activities and protein expression. In rats, region-specific, time- and dose-dependent reductions of NHE2 and NHE3 activities, protein expression, and mRNA were observed after exposure to IFN-gamma. Chronic exposure of intestinal epithelial cells to IFN-gamma results in selective downregulation of NHE2 and NHE3 expression and activity, a potential cause of inflammation-associated diarrhea.

摘要

传统上,炎症性肠病相关的腹泻被归因于刺激分泌。本研究的目的是确定干扰素-γ(IFN-γ)对大鼠肠道和Caco-2/bbe(C2)细胞肠黏膜的慢性刺激是否会影响顶端膜Na(+)/H(+)交换体NHE2和NHE3的表达及功能。用IFN-γ处理表达NHE2和NHE3的汇合C2细胞2、24和48小时。成年大鼠腹腔注射IFN-γ 12和48小时。通过跨C2细胞和大鼠刷状缘膜囊泡的单向(22)Na内流来测量NHE2和NHE3的活性。通过蛋白质免疫印迹法和Northern印迹法评估NHE蛋白和mRNA。用IFN-γ处理C2单层细胞导致NHE2和NHE3活性及蛋白表达降低>50%。在大鼠中,暴露于IFN-γ后,观察到NHE2和NHE3活性、蛋白表达及mRNA呈区域特异性、时间和剂量依赖性降低。肠道上皮细胞长期暴露于IFN-γ会导致NHE2和NHE3表达及活性的选择性下调,这是炎症相关性腹泻的一个潜在原因。

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