Department of Internal Medicine, Roy J and Lucille A Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242, USA.
J Biol Chem. 2010 Oct 1;285(40):30523-30. doi: 10.1074/jbc.M110.150755. Epub 2010 Jul 30.
Epithelial Na(+) absorption is regulated by Nedd4-2, an E3 ubiquitin ligase that reduces expression of the epithelial Na(+) channel (ENaC) at the cell surface. Defects in this regulation cause Liddle syndrome, an inherited form of hypertension. Previous work found that Nedd4-2 functions through two distinct effects on trafficking, enhancing both ENaC endocytosis and ENaC degradation in lysosomes. To investigate the mechanism by which Nedd4-2 targets ENaC to lysosomes, we tested the role of hepatocyte growth factor-regulated tyrosine kinase substrate (Hrs), a component of the endosomal sorting complexes required for transport (ESCRT)-0 complex. We found that α-, β-, and γENaC each interact with Hrs. These interactions were enhanced by Nedd4-2 and were dependent on the catalytic function of Nedd4-2 as well as its WW domains. Mutation of ENaC PY motifs, responsible for inherited hypertension (Liddle syndrome), decreased Hrs binding to ENaC. Moreover, binding of ENaC to Hrs was reduced by dexamethasone/serum- and glucocorticoid-inducible kinase and cAMP, which are signaling pathways that inhibit Nedd4-2. Nedd4-2 bound to Hrs and catalyzed Hrs ubiquitination but did not alter Hrs protein levels. Expression of a dominant negative Hrs lacking its ubiquitin-interacting motif (Hrs-ΔUIM) increased ENaC surface expression and current. This occurred through reduced degradation of the cell surface pool of proteolytically activated ENaC, which enhanced its recycling to the cell surface. In contrast, Hrs-ΔUIM had no effect on degradation of uncleaved inactive channels. The data support a model in which Nedd4-2 induces binding of ENaC to Hrs, which mediates the sorting decision between ENaC degradation and recycling.
上皮钠(Na+)吸收受 Nedd4-2 调节,Nedd4-2 是一种 E3 泛素连接酶,可降低细胞表面上皮钠(Na+)通道(ENaC)的表达。这种调节的缺陷导致利德尔综合征,这是一种遗传性高血压形式。以前的工作发现,Nedd4-2 通过对运输的两种不同作用发挥作用,增强 ENaC 的内吞作用和溶酶体中的 ENaC 降解。为了研究 Nedd4-2 将 ENaC 靶向溶酶体的机制,我们测试了肝细胞生长因子调节的酪氨酸激酶底物(Hrs)的作用,Hrs 是内体分选复合物必需的运输(ESCRT)-0 复合物的组成部分。我们发现 α、β 和 γENaC 均与 Hrs 相互作用。这些相互作用受 Nedd4-2 增强,并且依赖于 Nedd4-2 的催化功能及其 WW 结构域。负责遗传性高血压(利德尔综合征)的 ENaC PY 基序的突变降低了 Hrs 与 ENaC 的结合。此外,地塞米松/血清和糖皮质激素诱导的激酶和 cAMP 减少了 ENaC 与 Hrs 的结合,这两种信号通路可抑制 Nedd4-2。Nedd4-2 与 Hrs 结合并催化 Hrs 泛素化,但不改变 Hrs 蛋白水平。表达缺乏其泛素相互作用基序(Hrs-ΔUIM)的显性负性 Hrs 增加了 ENaC 的表面表达和电流。这是通过减少蛋白水解激活的 ENaC 细胞表面池的降解来实现的,这增强了其向细胞表面的再循环。相比之下,Hrs-ΔUIM 对未切割的无活性通道的降解没有影响。数据支持这样一种模型,即 Nedd4-2 诱导 ENaC 与 Hrs 结合,从而介导 ENaC 降解和再循环之间的分拣决策。