The calmodulin-binding tetraleucine motif of KCNE4 is responsible for association with Kv1.3.
intracellular retention
leukocytes
potassium channels
regulatory subunits
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
ISSN: 1530-6860
Titre abrégé: FASEB J
Pays: United States
ID NLM: 8804484
Informations de publication
Date de publication:
07 2019
07 2019
Historique:
pubmed:
11
4
2019
medline:
20
5
2020
entrez:
11
4
2019
Statut:
ppublish
Résumé
The voltage-dependent potassium (Kv) channel Kv1.3 regulates leukocyte proliferation, activation, and apoptosis, and altered expression of this channel is linked to autoimmune diseases. Thus, the fine-tuning of Kv1.3 function is crucial for the immune system response. The Kv1.3 accessory protein, potassium voltage-gated channel subfamily E (KCNE) subunit 4, acts as a dominant negative regulatory subunit to both enhance inactivation and induce intracellular retention of Kv1.3. Mutations in KCNE4 also cause immune system dysfunction. Although the formation of Kv1.3-KCNE4 complexes has profound consequences for leukocyte physiology, the molecular determinants involved in the Kv1.3-KCNE4 association are unknown. We now show that KCNE4 associates with Kv1.3
Identifiants
pubmed: 30969795
doi: 10.1096/fj.201801164RR
doi:
Substances chimiques
KCNE4 protein, human
0
KCNE4 protein, mouse
0
KCNE4 protein, rat
0
Kv1.3 Potassium Channel
0
Potassium Channels, Voltage-Gated
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM