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Nedd4-2 连接酶对人 Na+/H+ 交换蛋白 3(NHE3)的独特调节作用不同于非灵长类动物的 NHE3。

Unique regulation of human Na+/H+ exchanger 3 (NHE3) by Nedd4-2 ligase that differs from non-primate NHE3s.

机构信息

From the Division of Digestive Diseases, Department of Medicine and.

From the Division of Digestive Diseases, Department of Medicine and Winship Cancer Institute, Emory University, Atlanta, Georgia 30322

出版信息

J Biol Chem. 2014 Jun 27;289(26):18360-72. doi: 10.1074/jbc.M113.541706. Epub 2014 May 15.

Abstract

Na(+)/H(+) exchanger NHE3 expressed in the intestine and kidney plays a major role in NaCl and HCO3 (-) absorption that is closely linked to fluid absorption and blood pressure regulation. The Nedd4 family of E3 ubiquitin ligases interacts with a number of transporters and channels via PY motifs. A comparison of NHE3 sequences revealed the presence of PY motifs in NHE3s from human and several non-human primates but not in non-primate NHE3s. In this study we evaluated the differences between human and non-primate NHE3s in ubiquitination and interaction with Nedd4-2. We found that Nedd4-2 ubiquitinated human NHE3 (hNHE3) and altered its expression and activity. Surprisingly, rat NHE3 co-immunoprecipitated Nedd4-2, but its expression and activity were not altered by silencing of Nedd4-2. Ubiquitination by Nedd4-2 rendered hNHE3 to undergo internalization at a significantly greater rate than non-primate NHE3s without altering protein stability. Insertion of a PY motif in rabbit NHE3 recapitulated the interaction with Nedd4-2 and enhanced internalization. Thus, we propose a new model where disruption of Nedd4-2 interaction elevates hNHE3 expression and activity.

摘要

肠道和肾脏中表达的 Na(+)/H(+) 交换器 NHE3 在 NaCl 和 HCO3 (-) 的吸收中起主要作用,而这与液体吸收和血压调节密切相关。E3 泛素连接酶 Nedd4 家族通过 PY 基序与许多转运体和通道相互作用。对 NHE3 序列的比较表明,人类和一些非人类灵长类动物的 NHE3 中存在 PY 基序,但在非灵长类动物的 NHE3 中不存在。在这项研究中,我们评估了人源和非灵长类 NHE3 在泛素化和与 Nedd4-2 相互作用方面的差异。我们发现,Nedd4-2 泛素化人源 NHE3(hNHE3)并改变其表达和活性。令人惊讶的是,大鼠 NHE3 与 Nedd4-2 共免疫沉淀,但沉默 Nedd4-2 并不改变其表达和活性。Nedd4-2 的泛素化使 hNHE3 内化的速度比非灵长类 NHE3 快得多,而不改变蛋白稳定性。在兔 NHE3 中插入 PY 基序可重现与 Nedd4-2 的相互作用并增强内化。因此,我们提出了一个新的模型,即破坏 Nedd4-2 的相互作用会增加 hNHE3 的表达和活性。

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