4.4 Article

Trafficking of the IKs-Complex in MDCK Cells: Site of Subunit Assembly and Determinants of Polarized Localization

Journal

TRAFFIC
Volume 14, Issue 4, Pages 399-411

Publisher

WILEY
DOI: 10.1111/tra.12042

Keywords

KCNE1; KCNQ1; MDCK; trafficking; LQT; Rab1

Categories

Funding

  1. Novo Nordisk Foundation
  2. Aase and Ejnar Danielsens Fond
  3. Danish National Research Foundation
  4. Danish Heart Foundation [10-04-R78-A2791-22612, 09-04-R72-A2403-22543, 08-10-R68-A2189-B999-22496]

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The voltage-gated potassium channel KV7.1 is regulated by non-pore forming regulatory KCNE -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 KV7.1 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 KV7.1 targets the IKs-complex to the basolateral membrane, but that KCNE1 can redirect the complex to the apical membrane upon mutation of critical KV7.1 basolateral targeting signals. Our data provide a possible explanation to the fact that KV7.1 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 KV7.1/KCNE complexes.

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