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

Jens-Peter David, Martin N Andersen, Søren-Peter Olesen, Hanne B Rasmussen, Nicole Schmitt

Research output: Contribution to journalJournal articleResearchpeer-review

11 Citations (Scopus)

Abstract

The voltage-gated potassium channel K 7.1 is regulated by non-pore forming regulatory KCNE ß-subunits. Together with KCNE1, it forms the slowly activating delayed rectifier potassium current I . However, where the subunits assemble and which of the subunits determines localization of the I -complex has not been unequivocally resolved yet. We employed trafficking-deficient K 7.1 and KCNE1 mutants to investigate I 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 K 7.1 targets the I -complex to the basolateral membrane, but that KCNE1 can redirect the complex to the apical membrane upon mutation of critical K 7.1 basolateral targeting signals. Our data provide a possible explanation to the fact that K 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 K 7.1/KCNE complexes.
Original languageEnglish
JournalTraffic
Volume14
Issue number4
Pages (from-to)399-411
Number of pages13
ISSN1398-9219
DOIs
Publication statusPublished - Apr 2013

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