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Eph-B4 regulates adaptive venous remodeling to improve arteriovenous fistula patency

机译:Eph-B4调节自适应静脉重塑以改善动静脉瘘通畅

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Low rates of arteriovenous fistula (AVF) maturation prevent optimal fistula use for hemodialysis; however, the mechanism of venous remodeling in the fistula environment is not well understood. We hypothesized that the embryonic venous determinant Eph-B4 mediates AVF maturation. In human AVF and a mouse aortocaval fistula model, Eph-B4 protein expression increased in the fistula vein; expression of the arterial determinant Ephrin-B2 also increased. Stimulation of Eph-B-mediated signaling with Ephrin-B2/Fc showed improved fistula patency with less wall thickness. Mutagenesis studies showed that tyrosine-774 is critical for Eph-B4 signaling and administration of inactive Eph-B4-Y774F increased fistula wall thickness. Akt1 expression also increased in AVF; Akt1 knockout mice showed reduced fistula diameter and wall thickness. In Akt1 knockout mice, stimulation of Eph-B signaling with Ephrin-B2/Fc showed no effect on remodeling. These results show that AVF maturation is associated with acquisition of dual arteriovenous identity; increased Eph-B activity improves AVF patency. Inhibition of Akt1 function abolishes Eph-B-mediated venous remodeling suggesting that Eph-B4 regulates AVF venous adaptation through an Akt1-mediated mechanism.
机译:动静脉瘘(AVF)成熟率低,妨碍了最佳的瘘管用于血液透析;然而,在瘘管环境中静脉重塑的机制尚不清楚。我们假设,胚胎静脉决定簇Eph-B4介导AVF成熟。在人AVF和小鼠主动脉腔瘘模型中,Eph-B4蛋白在瘘静脉中的表达增加。动脉决定簇Ephrin-B2的表达也增加。用Ephrin-B2 / Fc刺激Eph-B介导的信号显示瘘管通畅性改善,壁厚更小。诱变研究表明,酪氨酸774对于Eph-B4信号传导至关重要,无活性Eph-B4-Y774F的给药会增加瘘管壁厚度。 AVF中Akt1表达也增加; Akt1基因敲除小鼠显示减少的瘘管直径和壁厚。在Akt1基因敲除小鼠中,用Ephrin-B2 / Fc刺激Eph-B信号传导对重构没有影响。这些结果表明AVF的成熟与双动静脉身份的获得有关。 Eph-B活性增加可提高AVF通畅性。抑制Akt1功能消除了Eph-B介导的静脉重构,表明Eph-B4通过Akt1介导的机制调节AVF静脉适应。

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