Department of Anesthesiology

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KCNE2 forms potassium channels with KCNA3 and KCNQ1 in the choroid plexus epithelium.

TitleKCNE2 forms potassium channels with KCNA3 and KCNQ1 in the choroid plexus epithelium.
Publication TypeJournal Article
Year of Publication2011
AuthorsRoepke TK, Kanda VA, Purtell K, King EC, Lerner DJ, Abbott GW
JournalFASEB J
Volume25
Issue12
Pagination4264-73
Date Published2011 Dec
ISSN1530-6860
KeywordsAnimals, Chlorides, Choroid Plexus, Epithelium, Ion Transport, KCNQ1 Potassium Channel, Kv1.3 Potassium Channel, Membrane Potentials, Mice, Mice, Knockout, Models, Biological, Potassium Channels, Voltage-Gated, Protein Subunits
Abstract

Cerebrospinal fluid (CSF) is crucial for normal function and mechanical protection of the CNS. The choroid plexus epithelium (CPe) is primarily responsible for secreting CSF and regulating its composition by mechanisms currently not fully understood. Previously, the heteromeric KCNQ1-KCNE2 K(+) channel was functionally linked to epithelial processes including gastric acid secretion and thyroid hormone biosynthesis. Here, using Kcne2(-/-) tissue as a negative control, we found cerebral expression of KCNE2 to be markedly enriched in the CPe apical membrane, where we also discovered expression of KCNQ1. Targeted Kcne2 gene deletion in C57B6 mice increased CPe outward K(+) current 2-fold. The Kcne2 deletion-enhanced portion of the current was inhibited by XE991 (10 μM) and margatoxin (10 μM) but not by dendrotoxin (100 nM), indicating that it arose from augmentation of KCNQ subfamily and KCNA3 but not KCNA1 K(+) channel activity. Kcne2 deletion in C57B6 mice also altered the polarity of CPe KCNQ1 and KCNA3 trafficking, hyperpolarized the CPe membrane by 9 ± 2 mV, and increased CSF [Cl(-)] by 14% compared with wild-type mice. These findings constitute the first report of CPe dysfunction caused by cation channel gene disruption and suggest that KCNE2 influences blood-CSF anion flux by regulating KCNQ1 and KCNA3 in the CPe.

DOI10.1096/fj.11-187609
Alternate JournalFASEB J.
PubMed ID21859894
PubMed Central IDPMC3236621
Grant ListR01 HL079275 / HL / NHLBI NIH HHS / United States
R01-HL079275 / HL / NHLBI NIH HHS / United States
T32-GM073546 / GM / NIGMS NIH HHS / United States