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首页> 外文期刊>American Journal of Physiology >Ezrin regulates the expression of Mrp2/Abcc2 and Mdr1/Abcb1 along the rat small intestinal tract
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Ezrin regulates the expression of Mrp2/Abcc2 and Mdr1/Abcb1 along the rat small intestinal tract

机译:Ezrin调节大鼠小肠Mrp2 / Abcc2和Mdr1 / Abcb1的表达

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Multidrug resistance-associated protein 2 (MRP2)/ATP-binding cassette protein C2 (ABCC2) and multidrug resistance protein 1 (MDR1)/ABCB1 are well-known efflux transporters located on the brush border membrane of the small intestinal epithelia, where they limit the absorption of a broad range of substrates. The expression patterns of MRP2/ABCC2 and MDR1/ABCB1 along the small intestinal tract are tightly regulated. Several reports have demonstrated the participation of ERM (ezrin/radixin/moesin) proteins in the posttranslational modulation of MRP2/ABCC2 and MDR1/ABCB1, especially with regard to their membrane localization. The present study focused on the in vivo expression profiles of MRP2/ABCC2, MDR1/ABCB1, ezrin, and phosphorylated ezrin to further elucidate the relationship between the efflux transporters and the ERM proteins. The current results showed good correlation between the phosphorylation status of ezrin and Mrp2/Abcc2 expression along the gastrointestinal tract of rats and between the expression profiles of both ezrin and Mdr1/Abcb1 in the small intestine. We also demonstrated the involvement of conventional protein kinase C isoforms in the regulation of ezrin phosphorylation. Furthermore, experiments conducted with wild-type (WT) ezrin and a T567A (Ala substituted Thr) dephosphorylated mutant showed a decrease in membrane surface-localized and total expressed MRP2/ABCC2 in T567A-expressing vs. WT ezrin-expressing Caco-2 cells. In contrast, T567A-and WT-expressing cells both showed an increase in membrane surface-localized and total expressed MDR1/ ABCB1. These findings suggest that the phosphorylation status and the expression profile of ezrin differentially direct MRP2/ABCC2 and MDR1/ABCB1 expression, respectively, along the small intestinal tract.
机译:多药耐药相关蛋白2(MRP2)/ ATP结合盒蛋白C2(ABCC2)和多药耐药蛋白1(MDR1)/ ABCB1是位于小肠上皮刷状缘膜上的著名外排转运蛋白吸收各种基材。 MRP2 / ABCC2和MDR1 / ABCB1在小肠的表达模式受到严格调节。几篇报道表明,ERM(ezrin / radixin / moesin)蛋白参与了MRP2 / ABCC2和MDR1 / ABCB1的翻译后调控,特别是在膜定位方面。本研究集中于MRP2 / ABCC2,MDR1 / ABCB1,ezrin和磷酸化的ezrin的体内表达谱,以进一步阐明外排转运蛋白和ERM蛋白之间的关系。目前的结果表明,ezrin的磷酸化状态与沿大鼠胃肠道的Mrp2 / Abcc2表达之间以及小肠中的ezrin和Mdr1 / Abcb1表达谱之间都具有良好的相关性。我们还证明了常规蛋白激酶C同工型参与ezrin磷酸化的调节。此外,用野生型(WT)ezrin和T567A(Ala取代的Thr)去磷酸化突变体进行的实验显示,与表达WT ezrin的Caco-2细胞相比,膜表面定位和总表达的MRP2 / ABCC2减少了。相比之下,T567A和WT表达细胞都显示膜表面定位和总表达的MDR1 / ABCB1增加。这些发现表明,ezrin的磷酸化状态和表达谱分别沿着小肠差异地指导MRP2 / ABCC2和MDR1 / ABCB1表达。

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