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