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5-羟二十碳四烯酸和白三烯 D4 增加肠道上皮细胞的旁细胞通透性。

5-Hydroxyeicosatetraenoic acid and leukotriene D4 increase intestinal epithelial paracellular permeability.

机构信息

Departament de Fisiologia, Facultat de Farmàcia, Universitat de Barcelona, 08028 Barcelona, Spain.

出版信息

Int J Biochem Cell Biol. 2013 Jul;45(7):1318-26. doi: 10.1016/j.biocel.2013.04.005. Epub 2013 Apr 10.

DOI:10.1016/j.biocel.2013.04.005
PMID:23583294
Abstract

The loss of epithelial barrier function plays a crucial role in the pathogenesis of inflammatory bowel disease, with levels of 5-lipoxygenase metabolites being increased in the mucosa of these patients. The objective of this study was to determine the effect of the eicosanoids produced by the 5-lipoxygenase pathway, leukotriene B4 and D4, and 5-hydroxyeicosatetraenoic acid on epithelial barrier function. Paracellular permeability was estimated from fluorescein isothiocyanate-dextran fluxes and transepithelial electrical resistance in differentiated Caco-2 cells. Our results suggest that leukotriene D4 and 5-hydroxyeicosatetraenoic acid altered both parameters. Identification of the receptors involved in these changes indicated that cysteinyl-leukotriene receptor 1 participates in the effects of leukotriene D4. For both eicosanoids, these effects were mediated by activation of the phospholipase C/Ca(2+)/protein kinase C pathway, in addition to cAMP-independent protein kinase A activation. Furthermore, we observed a correlation between increased paracellular permeability and the redistribution of occludin, and for leukotriene D4, the disorganization of the subapical actin ring and myosin light chain kinase activation. In conclusion, on the basis of our results, we propose that 5-lipoxygenase pathway metabolites participate in the disruption of epithelial barrier function that is characteristic of inflammatory bowel disease.

摘要

上皮屏障功能的丧失在炎症性肠病的发病机制中起着关键作用,这些患者的黏膜中 5-脂氧合酶代谢物的水平增加。本研究的目的是确定 5-脂氧合酶途径产生的类二十烷酸,白三烯 B4 和 D4 以及 5-羟二十碳四烯酸对上皮屏障功能的影响。通过荧光素异硫氰酸酯-葡聚糖通量和分化的 Caco-2 细胞中的跨上皮电阻来估计旁细胞通透性。我们的结果表明白三烯 D4 和 5-羟二十碳四烯酸改变了这两个参数。参与这些变化的受体的鉴定表明半胱氨酰白三烯受体 1 参与了白三烯 D4 的作用。对于这两种类二十烷酸,这些作用是通过激活磷脂酶 C/Ca(2+)/蛋白激酶 C 途径介导的,除了 cAMP 非依赖性蛋白激酶 A 激活。此外,我们观察到旁细胞通透性增加与闭合蛋白重分布之间存在相关性,对于白三烯 D4,还观察到亚顶点肌动球蛋白环的紊乱和肌球蛋白轻链激酶的激活。总之,根据我们的结果,我们提出 5-脂氧合酶途径代谢物参与了炎症性肠病特征性的上皮屏障功能破坏。

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