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AUP1调节NKCC2的内质网相关降解和多聚泛素化。

AUP1 Regulates the Endoplasmic Reticulum-Associated Degradation and Polyubiquitination of NKCC2.

作者信息

Frachon Nadia, Demaretz Sylvie, Seaayfan Elie, Chelbi Lydia, Bakhos-Douaihy Dalal, Laghmani Kamel

机构信息

Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, Université de Paris, F-75006 Paris, France.

CNRS, ERL8228, F-75006 Paris, France.

出版信息

Cells. 2024 Feb 24;13(5):389. doi: 10.3390/cells13050389.

Abstract

Inactivating mutations of kidney Na-K-2Cl cotransporter NKCC2 lead to antenatal Bartter syndrome (BS) type 1, a life-threatening salt-losing tubulopathy. We previously reported that this serious inherited renal disease is linked to the endoplasmic reticulum-associated degradation (ERAD) pathway. The purpose of this work is to characterize further the ERAD machinery of NKCC2. Here, we report the identification of ancient ubiquitous protein 1 (AUP1) as a novel interactor of NKCC2 ER-resident form in renal cells. AUP1 is also an interactor of the ER lectin OS9, a key player in the ERAD of NKCC2. Similar to OS9, AUP1 co-expression decreased the amount of total NKCC2 protein by enhancing the ER retention and associated protein degradation of the cotransporter. Blocking the ERAD pathway with the proteasome inhibitor MG132 or the α-mannosidase inhibitor kifunensine fully abolished the AUP1 effect on NKCC2. Importantly, AUP1 knock-down or inhibition by overexpressing its dominant negative form strikingly decreased NKCC2 polyubiquitination and increased the protein level of the cotransporter. Interestingly, AUP1 co-expression produced a more profound impact on NKCC2 folding mutants. Moreover, AUP1 also interacted with the related kidney cotransporter NCC and downregulated its expression, strongly indicating that AUP1 is a common regulator of sodium-dependent chloride cotransporters. In conclusion, our data reveal the presence of an AUP1-mediated pathway enhancing the polyubiquitination and ERAD of NKCC2. The characterization and selective regulation of specific ERAD constituents of NKCC2 and its pathogenic mutants could open new avenues in the therapeutic strategies for type 1 BS treatment.

摘要

肾脏钠-钾-2氯协同转运蛋白NKCC2的失活突变会导致1型产前巴特综合征(BS),这是一种危及生命的失盐性肾小管病。我们之前报道过,这种严重的遗传性肾病与内质网相关降解(ERAD)途径有关。这项工作的目的是进一步表征NKCC2的ERAD机制。在此,我们报告鉴定出古老泛在蛋白1(AUP1)是肾细胞中NKCC2内质网驻留形式的一种新型相互作用蛋白。AUP1也是内质网凝集素OS9的相互作用蛋白,而OS9是NKCC2的ERAD中的关键因子。与OS9相似,AUP1的共表达通过增强协同转运蛋白的内质网滞留及相关蛋白降解,降低了总NKCC2蛋白的量。用蛋白酶体抑制剂MG132或α-甘露糖苷酶抑制剂 kifunensine阻断ERAD途径可完全消除AUP1对NKCC2的影响。重要的是,敲低AUP1或过表达其显性负性形式对其进行抑制,可显著降低NKCC2的多聚泛素化,并增加协同转运蛋白的蛋白水平。有趣的是,AUP1的共表达对NKCC2折叠突变体产生了更深远的影响。此外,AUP1还与相关的肾脏协同转运蛋白NCC相互作用,并下调其表达,强烈表明AUP1是钠依赖性氯协同转运蛋白的共同调节因子。总之,我们的数据揭示了存在一条由AUP1介导的增强NKCC2多聚泛素化和ERAD的途径。对NKCC2及其致病突变体的特定ERAD成分进行表征和选择性调控,可能为1型BS的治疗策略开辟新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ef7/10931229/7e21cb26d009/cells-13-00389-g001.jpg

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