Yamagata K, Tagami M, Takenaga F, Yamori Y, Nara Y, Itoh S
Division of Life Science, Graduate School of Integrated Science and Art, University of East Asia, Shimonoseki, Yamaguchi, Japan.
Neuroscience. 2003;116(3):649-56. doi: 10.1016/s0306-4522(02)00715-7.
Tight junctions create a rate-limiting barrier to the diffusion of solutes between vertebrate epithelial cells and endothelial cells. They are also controlled within individual cells by a variety of physiologically relevant signals. We investigated the effects of polyunsaturated fatty acids on the formation of tight junctions in brain capillary endothelial cells, monitoring the transepithelial electrical resistance, and analyzed the expression of occludin messenger RNA. Brain-capillary endothelial cells were grown to confluence on filters and exposed to eicosapentaenoic acids, gamma linolenic acid and linoleic acid. Transepithelial electrical resistance was determined with voltage-measuring electrodes. The messenger RNA expression of occludin was quantitated by real-time quantitative reverse transcriptase-polymerase chain reaction. The basal resistance across monolayers of porcine brain capillary endothelial cells was 83+/-8.1 Omega cm(2). Cells cultured in eicosapentaenoic acids and gamma linolenic acid, but not linolenic acid, displayed a 2.7-fold increase in transepithelial electrical resistance at 10 microM in brain capillary endothelial cells. The expression level of occludin messenger RNA increased markedly immediately after the exposure to eicosapentaenoic acids or gamma linolenic acid. Following an 8 h exposure to exogenous eicosapentaenoic acids or gamma linolenic acid, occludin messenger RNA levels were significantly increased. In addition, the rise in transepithelial electrical resistance induced by eicosapentaenoic acids and gamma linolenic acid was markedly inhibited by the tyrosine kinase inhibitors genistein and PP2 and protein kinase C inhibitor, calphostin C. In contrast, the rise in transepithelial electrical resistance induced by eicosapentaenoic acids and gamma linolenic acid was not inhibited by the PI 3-kinase inhibitor, LY294002. We conclude that eicosapentaenoic acids and gamma linolenic acid increased the transepithelial electrical resistance and the expression of occludin messenger RNA in brain capillary endothelial cells. This gamma linolenic acid and eicosapentaenoic acid induced assembly of tight junction is likely to be regulated by protein kinase C and tyrosine kinase activity.
紧密连接对溶质在脊椎动物上皮细胞和内皮细胞之间的扩散形成了限速屏障。它们在单个细胞内也受到多种生理相关信号的调控。我们研究了多不饱和脂肪酸对脑毛细血管内皮细胞紧密连接形成的影响,监测跨上皮电阻,并分析了闭合蛋白信使核糖核酸的表达。将脑毛细血管内皮细胞在滤器上培养至汇合,然后分别用二十碳五烯酸、γ-亚麻酸和亚油酸处理。用电压测量电极测定跨上皮电阻。通过实时定量逆转录聚合酶链反应对闭合蛋白的信使核糖核酸表达进行定量。猪脑毛细血管内皮细胞单层的基础电阻为83±8.1Ω·cm²。在脑毛细血管内皮细胞中,用二十碳五烯酸和γ-亚麻酸而非亚麻酸培养的细胞,在10μM时跨上皮电阻增加了2.7倍。暴露于二十碳五烯酸或γ-亚麻酸后,闭合蛋白信使核糖核酸的表达水平立即显著增加。在暴露于外源性二十碳五烯酸或γ-亚麻酸8小时后,闭合蛋白信使核糖核酸水平显著升高。此外,酪氨酸激酶抑制剂染料木黄酮和PP2以及蛋白激酶C抑制剂钙泊三醇可显著抑制二十碳五烯酸和γ-亚麻酸诱导的跨上皮电阻升高。相比之下,PI 3-激酶抑制剂LY294002对二十碳五烯酸和γ-亚麻酸诱导的跨上皮电阻升高没有抑制作用。我们得出结论,二十碳五烯酸和γ-亚麻酸增加了脑毛细血管内皮细胞的跨上皮电阻和闭合蛋白信使核糖核酸的表达。这种由γ-亚麻酸和二十碳五烯酸诱导的紧密连接组装可能受蛋白激酶C和酪氨酸激酶活性的调节。