Chung, JoshuaJoshuaChungTilūnaitė, AgnėAgnėTilūnaitėLadd, DavidDavidLaddHunt, HilaryHilaryHuntSoeller, Johannes ChristianJohannes ChristianSoellerCrampin, Edmund JEdmund JCrampinJohnston, Stuart TStuart TJohnstonRoderick, H LlewelynH LlewelynRoderickRajagopal, VijayVijayRajagopal2024-10-112024-10-112023-01https://boris-portal.unibe.ch/handle/20.500.12422/88958Calcium (Ca2＋) plays a critical role in the excitation contraction coupling (ECC) process that mediates the contraction of cardiomyocytes during each heartbeat. While ryanodine receptors (RyRs) are the primary Ca2＋ channels responsible for generating the cell-wide Ca2＋ transients during ECC, Ca2＋ release, a=via inositol 1,4,5-trisphosphate (IP3) receptors (IP3Rs) are also reported in cardiomyocytes and to elicit ECC-modulating effects. Recent studies suggest that the localization of IP3Rs at dyads grant their ability to modify the occurrence of Ca2＋ sparks (elementary Ca2＋ release events that constitute cell wide Ca2＋ releases associated with ECC) which may underlie their modulatory influence on ECC. Here, we aim to uncover the mechanism by which dyad-localized IP3Rs influence Ca2＋ spark dynamics. To this end, we developed a mathematical model of the dyad that incorporates the behaviour of IP3Rs, in addition to RyRs, to reveal the impact of their activity on local Ca2＋ handling and consequent Ca2＋ spark occurrence and its properties. Consistent with published experimental data, our model predicts that the propensity for Ca2＋ spark formation increases in the presence of IP3R activity. Our simulations support the hypothesis that IP3Rs elevate Ca2＋ in the dyad, sensitizing proximal RyRs toward activation and hence Ca2＋ spark formation. The stochasticity of IP3R gating is an important aspect of this mechanism. However, dyadic IP3R activity lowers the Ca2＋ available in the junctional sarcoplasmic reticulum (JSR) for release, thus resulting in Ca2＋ sparks with similar durations but lower amplitudes.enCa(2＋) microdomains Ca(2＋) sparks Calcium Cardiomyocyte IP(3)R RyR600 - Technology::610 - Medicine & healtharticle10.48350/1748653639582710.1016/j.mbs.2022.108923