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Distinct effects of protein kinase C on the barrier function at different developmental stages

机译:蛋白激酶C在不同发育阶段对屏障功能的不同影响

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We show here, that activation of protein kinase C by the phorbol ester PMA improves barrier function in colon carcinoma (HT 29) cells. By contrast, in canine kidney (MDCK I) cells it caused increased permeability and opening of tight junctions; thelatter has also been noticed in other studies. Thus, with PMA confluent HT 29 cells responded with a reduced passage of 330 kDa sodium fluorescein, increased transepithelial electrical resistance, and a change in the cell shape of the HT 29 cells from anirregular to a regular, hexagonal form. Confocal imaging revealed parallel distinct changes in the staining of occludin and caludin-1, viz. a translation from cytoplasmic clusters to apical cell-cell contacts. Interestingly, in both cell lines protein kinase A activation caused a decreased in the threonine phosphorylation of occludin that correlated with tight junction assembly in HT 29 cells and tight junction disassembly in MDCK I cells. We conclude that protein kinase C regulation of the epithelialbarrier involves specific molecular mechanisms and achieves distinct effects at different developmental stages.
机译:我们在这里表明,佛波酯PMA激活蛋白激酶C可以改善结肠癌(HT 29)细胞的屏障功能。相反,在犬肾脏(MDCK I)细胞中,它导致通透性增加和紧密连接的打开;其他研究也注意到了这一点。因此,使用PMA融合的HT 29细胞,其通过的330 kDa荧光素钠传递减少,跨上皮电阻增加,并且HT 29细胞的细胞形状从不规则形状变为规则的六角形。共聚焦成像揭示了occludin和caludin-1染色的平行平行变化,即。从细胞质簇到顶端细胞间接触的翻译。有趣的是,在这两种细胞系中,蛋白激酶A的激活都会导致occludin的苏氨酸磷酸化降低,这与HT 29细胞中的紧密连接装配和MDCK I细胞中的紧密连接拆卸有关。我们得出结论,上皮屏障的蛋白激酶C调节涉及特定的分子机制,并在不同的发育阶段达到独特的效果。

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