Meyer zum Büschenfelde Dirk, Tauber Rudolf, Huber Otmar
Department of Laboratory Medicine and Pathobiochemistry, Charité-Campus Benjamin Franklin, Hindenburgdamm 30, 12200 Berlin, Germany.
Peptides. 2006 Dec;27(12):3383-90. doi: 10.1016/j.peptides.2006.08.020. Epub 2006 Oct 2.
TFF3 plays an important role in the protection and repair of the gastrointestinal mucosa. The molecular mechanisms of TFF function, however, are still largely unknown. Increasing evidence indicates that apart from stabilizing mucosal mucins TFF3 induces cellular signals that modulate cell-cell junctions of epithelia. In transfected HT29/B6 and MDCK cells stably expressing FLAG-tagged human TFF3 we have recently shown that TFF3 down-regulates E-cadherin, impairs the function of adherens junctions and thus facilitates cell migration in wounded epithelial cell layers. Here we investigate TFF3-induced effects on the composition and function of tight junctions in these cells. TFF3 increased the cellular level of tightening claudin-1 and decreased the amount of claudin-2 known to form cation-selective channels. Expression of ZO-1, ZO-2 and occludin was not altered. The change in claudin-1 and -2 expression in TFF3-expressing HT29/B6 cells was accompanied by an increase in the transepithelial resistance in confluent monolayers of these cells. These data suggest that TFF3 plays a role in the regulation of intestinal barrier function by altering the claudin composition within tight junctions thus decreasing paracellular permeability of the intestinal mucosa.
三叶因子3(TFF3)在胃肠道黏膜的保护和修复中发挥着重要作用。然而,TFF功能的分子机制仍大多未知。越来越多的证据表明,除了稳定黏膜黏蛋白外,TFF3还能诱导调节上皮细胞间连接的细胞信号。最近,在稳定表达FLAG标签的人TFF3的转染HT29/B6和MDCK细胞中,我们发现TFF3下调E-钙黏蛋白,损害黏附连接的功能,从而促进受伤上皮细胞层中的细胞迁移。在此,我们研究TFF3对这些细胞中紧密连接的组成和功能的影响。TFF3增加了紧密连接蛋白claudin-1的细胞水平,并减少了已知形成阳离子选择性通道的claudin-2的量。ZO-1、ZO-2和闭合蛋白的表达未发生改变。在表达TFF3的HT29/B6细胞中,claudin-1和-2表达的变化伴随着这些细胞汇合单层中跨上皮电阻的增加。这些数据表明,TFF3通过改变紧密连接中的claudin组成,从而降低肠黏膜的细胞旁通透性,在肠道屏障功能的调节中发挥作用。