首页> 外文期刊>American Journal of Physiology >FXYD5 (dysadherin) regulates the paracellular permeability in cultured kidney collecting duct cells.
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FXYD5 (dysadherin) regulates the paracellular permeability in cultured kidney collecting duct cells.

机译:FXYD5(Dysadherin)调节培养的肾脏收集管道细胞的肺细胞渗透性。

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摘要

FXYD5 (dysadherin or RIC) is a member of the FXYD family of single-span transmembrane proteins associated with the Na(+)-K(+)-ATPase. Several studies have demonstrated enhanced expression of FXYD5 during metastasis and effects on cell adhesion and motility. The current study examines effects of FXYD5 on the paracellular permeability in the mouse kidney collecting duct cell line M1. Expressing FXYD5 in these cells leads to a large decrease in amiloride-insensitive transepithelial electrical resistance as well as increased permeability to 4-kDa dextran. Impairment of cell-cell contact was also demonstrated by staining cells for the tight and adherence junction markers zonula occludens-1 and beta-catenin, respectively. This is further supported by large expansions of the interstitial spaces, visualized in electron microscope images. Expressing FXYD5 in M1 cells resulted in a decrease in N-glycosylation of beta1 Na(+)-K(+)-ATPase, while silencing it in H1299 cells had an opposite effect. This may provide a mechanism for the above effects, since normal glycosylation of beta1 plays an important role in cell-cell contact formation (Vagin O, Tokhtaeva E, Sachs G. J Biol Chem 281: 39573-39587, 2006).
机译:FXYD5(Dysadherin或Ric)是与Na(+) - K(+) - ATP酶相关的单跨跨膜蛋白的FXYD系列的成员。几项研究表明转移期间FXYD5的增强表达和对细胞粘附和运动的影响。目前的研究检查了FXYD5对小鼠肾脏收集管道细胞系M1中肺细胞渗透性的影响。在这些细胞中表达FXYD5导致余流量的不敏感的培养性培养性电阻的大大降低以及对4-KDA葡聚糖的渗透性增加。还通过分别染色细胞染色细胞来证明细胞细胞接触的损伤。这是通过在电子显微镜图像中可视化的大型膨胀空间的大扩展来进一步支持。在M1细胞中表达FXYD5导致β1Na(+) - K(+) - ATP酶的N-糖基化的降低,同时将其沉默于H1299细胞中具有相反的效果。这可以提供上述效果的机制,因为β1的正常糖基化在细胞 - 细胞接触形成中起重要作用(Vagin O,Tokhtaeva E,Sachs G.J Biol Chem 281:39573-39587,2006)。

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