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MDCK 细胞中 IKs 复合物的转运:亚基组装的位点和极性定位的决定因素。

Trafficking of the IKs -complex in MDCK cells: site of subunit assembly and determinants of polarized localization.

机构信息

The Ion Channel Group, Danish National Foundation Centre for Cardiac Arrhythmia, Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, 2200, Denmark.

出版信息

Traffic. 2013 Apr;14(4):399-411. doi: 10.1111/tra.12042. Epub 2013 Feb 13.

Abstract

The voltage-gated potassium channel KV 7.1 is regulated by non-pore forming regulatory KCNE β-subunits. Together with KCNE1, it forms the slowly activating delayed rectifier potassium current IKs . However, where the subunits assemble and which of the subunits determines localization of the IKs -complex has not been unequivocally resolved yet. We employed trafficking-deficient KV 7.1 and KCNE1 mutants to investigate IKs trafficking using the polarized Madin-Darby Canine Kidney cell line. We find that the assembly happens early in the secretory pathway but provide three lines of evidence that it takes place in a post-endoplasmic reticulum compartment. We demonstrate that KV 7.1 targets the IKs -complex to the basolateral membrane, but that KCNE1 can redirect the complex to the apical membrane upon mutation of critical KV 7.1 basolateral targeting signals. Our data provide a possible explanation to the fact that KV 7.1 can be localized apically or basolaterally in different epithelial tissues and offer a solution to divergent literature results regarding the effect of KCNE subunits on the subcellular localization of KV 7.1/KCNE complexes.

摘要

电压门控钾通道 KV 7.1 由非孔形成调节性 KCNEβ亚基调节。它与 KCNE1 一起形成缓慢激活的延迟整流钾电流 IKs。然而,亚基组装的位置以及哪些亚基决定 IKs 复合物的定位尚未得到明确解决。我们使用运输缺陷型 KV 7.1 和 KCNE1 突变体,使用极化的 Madin-Darby 犬肾细胞系研究 IKs 的运输。我们发现组装发生在分泌途径的早期,但有三条证据表明它发生在内质网后区室中。我们证明 KV 7.1 将 IKs 复合物靶向基底外侧膜,但 KCNE1 可以通过突变关键的 KV 7.1 基底外侧靶向信号将复合物重定向到顶膜。我们的数据为 KV 7.1 可以在不同的上皮组织中定位于基底外侧或顶侧的事实提供了一个可能的解释,并为关于 KCNE 亚基对 KV 7.1/KCNE 复合物亚细胞定位的影响的不同文献结果提供了一个解决方案。

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