Post-natal heart adaptation in a knock-in mouse model of calsequestrin 2-linked recessive catecholaminergic polymorphic ventricular tachycardia

Articolo
Data di Pubblicazione:
2014
Abstract:
Cardiaccalsequestrin(CASQ2)contributestointracellularCa2þ homeostasisbyvirtueofitslow- affinity/high-capacityCa2þ bindingproperties,maintainssarcoplasmicreticulum(SR)architectureand regulatesexcitation-contractioncoupling,especiallyorexclusivelyupon ?-adrenergicstimulation. Catecholaminergicpolymorphicventriculartachycardia(CPVT)isaninheritedarrhythmogenicdisease associatedwithcardiacarrestinchildrenoryoungadults.RecessiveCPVTvariantsaredueto mutationsintheCASQ2gene.Molecularandultra-structuralpropertieswerestudiedinheartsof CASQ2R33Q/R33Q and ofCASQ2/ mice frompost-natalday2toweek8.Thedrasticreductionof CASQ2-R33Qisanearlydevelopmentaleventandisaccompaniedbydown-regulationoftriadinand junctin,andmorphologicalchangesofjSRandofSR-transverse-tubulejunctions.Althoughendo- plasmic reticulumstressisactivated,nosignsofeither apoptosisorautophagyaredetected.Theother modelofrecessiveCPVT,theCASQ2/ mouse, doesnotdisplaythesameadaptivepattern. ExpressionofCASQ2-R33Qinfluences molecularandultra-structural heartdevelopment;post-natal, adaptivechangesappearcapableofensuringuntil adulthoodanewpathophysiologicalequilibrium.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
CASQ2 knock-out; CASQ2 mutation; Catecholaminergic polymorphic ventricular tachycardia; ER stress
Elenco autori:
Link alla scheda completa:
https://iris.cnr.it/handle/20.500.14243/288363
Pubblicato in:
EXPERIMENTAL CELL RESEARCH
Journal