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泛素连接酶Nedd4L调节结肠中的钠/钾/2氯共转运体NKCC1/SLC12A2。

The Ubiquitin Ligase Nedd4L Regulates the Na/K/2Cl Co-transporter NKCC1/SLC12A2 in the Colon.

作者信息

Jiang Chong, Kawabe Hiroshi, Rotin Daniela

机构信息

Hospital for Sick Children and University of Toronto, Toronto, Ontario M5G 0A4, Canada.

Department of Molecular Neurobiology, Max Planck Institute of Experimental Medicine, Hermann-Rein-Strasse 3D, 37075 Goettingen, Germany.

出版信息

J Biol Chem. 2017 Feb 24;292(8):3137-3145. doi: 10.1074/jbc.M116.770065. Epub 2017 Jan 13.

Abstract

The ubiquitin ligase Nedd4-like (Nedd4L, or Nedd4-2) binds to and regulates stability of the epithelial Na channel (ENaC) in salt-absorbing epithelia in the kidney, lung, and other tissues. Its role in the distal colon, which also absorbs salt and fluid and expresses ENaC, is unknown. Using a conditional knock-out approach to knock out in mice intestinal epithelium ( ; ) we show here that depletion leads to a higher steady-state short circuit current (Isc) in mouse distal colon tissue relative to controls. This higher Isc was partially reduced by the addition of apical amiloride and strongly reduced by basolateral bumetanide as well as by depletion of basolateral Cl, suggesting that Na/K/2Cl (NKCC1/SLC12A2) co-transporter and ENaC are targets of Nedd4L in the colon. In accordance, NKCC1 (and γENaC) protein abundance in the colon of the Nedd4L knock-out animals was increased, indicating that Nedd4L normally suppresses these proteins. However, we did not observe co-immunoprecipitation between Nedd4L and NKCC1, suggesting that Nedd4L indirectly suppresses NKCC1 expression. Low salt diet resulted in a strong increase in β and γ (but not α) ENaC mRNA and protein expression and ENaC activity. Although salt restriction also increased NKCC1 protein and mRNA abundance, it did not lead to its elevated activity (Isc). These results identify NKCC1 as a novel target for Nedd4L-mediated down-regulation , which modulates ion and fluid transport in the distal colon together with ENaC.

摘要

泛素连接酶Nedd4样蛋白(Nedd4L,即Nedd4-2)可与肾、肺及其他组织中负责盐吸收的上皮细胞中的上皮钠通道(ENaC)结合,并调节其稳定性。其在远端结肠(同样吸收盐和液体并表达ENaC)中的作用尚不清楚。我们采用条件性基因敲除方法在小鼠肠道上皮细胞中敲除(;),结果显示,与对照组相比,Nedd4L缺失导致小鼠远端结肠组织中的稳态短路电流(Isc)更高。添加顶端氨氯吡脒可部分降低这种较高的Isc,而基底侧布美他尼以及基底侧Cl耗尽则可使其大幅降低,这表明钠/钾/2氯共转运体(NKCC1/SLC12A2)和ENaC是结肠中Nedd4L的作用靶点。相应地,Nedd4L基因敲除动物结肠中NKCC1(和γENaC)的蛋白丰度增加,表明Nedd4L通常会抑制这些蛋白。然而,我们未观察到Nedd4L与NKCC1之间的共免疫沉淀现象,这表明Nedd4L间接抑制NKCC1的表达。低盐饮食导致β和γ(而非α)ENaC的mRNA和蛋白表达以及ENaC活性大幅增加。尽管盐限制也增加了NKCC1的蛋白和mRNA丰度,但并未导致其活性(Isc)升高。这些结果确定NKCC1是Nedd4L介导的下调作用的新靶点,它与ENaC一起调节远端结肠中的离子和液体转运。

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