RRC ID 60094
Author Yamada N, Asano Y, Fujita M, Yamazaki S, Inanobe A, Matsuura N, Kobayashi H, Ohno S, Ebana Y, Tsukamoto O, Ishino S, Takuwa A, Kioka H, Yamashita T, Hashimoto N, Zankov DP, Shimizu A, Asakura M, Asanuma H, Kato H, Nishida Y, Miyashita Y, Shinomiya H, Naiki N, Hayashi K, Makiyama T, Ogita H, Miura K, Ueshima H, Komuro I, Yamagishi M, Horie M, Kawakami K, Furukawa T, Koizumi A, Kurachi Y, Sakata Y, Minamino T, Kitakaze M, Takashima S.
Title Mutant KCNJ3 and KCNJ5 Potassium Channels as Novel Molecular Targets in Bradyarrhythmias and Atrial Fibrillation.
Journal Circulation
Abstract BACKGROUND:Bradyarrhythmia is a common clinical manifestation. Although the majority of cases are acquired, genetic analysis of families with bradyarrhythmia has identified a growing number of causative gene mutations. Because the only ultimate treatment for symptomatic bradyarrhythmia has been invasive surgical implantation of a pacemaker, the discovery of novel therapeutic molecular targets is necessary to improve prognosis and quality of life.
METHODS:We investigated a family containing 7 individuals with autosomal dominant bradyarrhythmias of sinus node dysfunction, atrial fibrillation with slow ventricular response, and atrioventricular block. To identify the causative mutation, we conducted the family-based whole exome sequencing and genome-wide linkage analysis. We characterized the mutation-related mechanisms based on the pathophysiology in vitro. After generating a transgenic animal model to confirm the human phenotypes of bradyarrhythmia, we also evaluated the efficacy of a newly identified molecular-targeted compound to upregulate heart rate in bradyarrhythmias by using the animal model.
RESULTS:We identified one heterozygous mutation, KCNJ3 c.247A>C, p.N83H, as a novel cause of hereditary bradyarrhythmias in this family. KCNJ3 encodes the inwardly rectifying potassium channel Kir3.1, which combines with Kir3.4 (encoded by KCNJ5) to form the acetylcholine-activated potassium channel ( IKACh channel) with specific expression in the atrium. An additional study using a genome cohort of 2185 patients with sporadic atrial fibrillation revealed another 5 rare mutations in KCNJ3 and KCNJ5, suggesting the relevance of both genes to these arrhythmias. Cellular electrophysiological studies revealed that the KCNJ3 p.N83H mutation caused a gain of IKACh channel function by increasing the basal current, even in the absence of m2 muscarinic receptor stimulation. We generated transgenic zebrafish expressing mutant human KCNJ3 in the atrium specifically. It is interesting to note that the selective IKACh channel blocker NIP-151 repressed the increased current and improved bradyarrhythmia phenotypes in the mutant zebrafish.
CONCLUSIONS:The IKACh channel is associated with the pathophysiology of bradyarrhythmia and atrial fibrillation, and the mutant IKACh channel ( KCNJ3 p.N83H) can be effectively inhibited by NIP-151, a selective IKACh channel blocker. Thus, the IKACh channel might be considered to be a suitable pharmacological target for patients who have bradyarrhythmia with a gain-of-function mutation in the IKACh channel.
Volume 139(18)
Pages 2157-2169
Published 2019-4-30
DOI 10.1161/CIRCULATIONAHA.118.036761
PMID 30764634
MeSH Amino Acid Substitution Animals Animals, Genetically Modified Atrial Fibrillation* / genetics Atrial Fibrillation* / metabolism Atrial Fibrillation* / pathology Atrial Fibrillation* / physiopathology Atrioventricular Block* / genetics Atrioventricular Block* / metabolism Atrioventricular Block* / pathology Atrioventricular Block* / physiopathology Benzopyrans / pharmacology Bradycardia* / genetics Bradycardia* / metabolism Bradycardia* / pathology Bradycardia* / physiopathology Electrophysiologic Techniques, Cardiac Female G Protein-Coupled Inwardly-Rectifying Potassium Channels* / antagonists & inhibitors G Protein-Coupled Inwardly-Rectifying Potassium Channels* / genetics G Protein-Coupled Inwardly-Rectifying Potassium Channels* / metabolism Genetic Diseases, Inborn* / genetics Genetic Diseases, Inborn* / metabolism Genetic Diseases, Inborn* / pathology Genetic Diseases, Inborn* / physiopathology Humans Male Mutation, Missense* Xenopus laevis Zebrafish
IF 23.054
Times Cited 4