Nos1ap Polymorphisms Reduce Nos1 Activity And Interact With Prolonged Repolarization In Arrhythmogenesis

Aims NOS1AP single-nucleotide polymorphisms (SNPs) correlate with QT prolongation and cardiac sudden death in patients affected by long QT syndrome type 1 (LQT1). NOS1AP targets NOS1 to intracellular effectors. We hypothesize that NOS1AP SNPs cause NOS1 dysfunction and this may converge with prolonged action-potential du-ration (APD) to facilitate arrhythmias. Here we test (i) the effects of NOS1 inhibition and their interaction with prolonged APD in a guinea pig cardiomyocyte (GP-CMs) LQT1 model; (ii) whether pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) from LQT1 patients differing for NOS IAP variants and mutation penetrance display a phenotype compatible with NOS1 deficiency.Methods and results In GP-CMs, NOS1 was inhibited by S-Methyl-L-thiocitrulline acetate (SMTC) or Vinyl-L-NIO hydrochloride (L-VNIO); LQT1 was mimicked by I-Ks blockade (JNJ303) and beta-adrenergic stimulation (isoproterenol). hiPSC-CMs were obtained from symptomatic (S) and asymptomatic (AS) KCNQ1-A341V carriers, harbouring the minor and major alleles of NOS IAP SNPs (rs16847548 and rs4657139), respectively. In GP-CMs, NOS1 inhibition prolonged APD, enhanced I-CaL and I-NaL, stowed Ca2+ decay, and induced delayed afterdepolarizations. Under action-potential damp, switching to shorter APD suppressed 'transient inward current' events induced by NOS1 inhibition and re-duced cytosolic Ca2+. In S (vs. AS) hiPSC-CMs, APD was longer and I-CaL larger; NOS1AP and NOS1 expression and co-localization were decreased.Conclusion The minor NOS1AP alleles are associated with NOS1 loss of function. The latter likely contributes to APD prolon-gation in LQT1 and converges with it to perturb Ca2+ handling. This establishes a mechanistic link between NOS IAP SNPs and aggravation of the arrhythmia phenotype in prolonged repolarization syndromes.[GRAPHICS].