Department of Physiology and Biophysics, Weill Medical College of Cornell University, New York, New York, United States of America.
PLoS Comput Biol. 2010 Dec 23;6(12):e1001041. doi: 10.1371/journal.pcbi.1001041.
The sinoatrial node (SAN) is a complex structure that exhibits anatomical and functional heterogeneity which may depend on: 1) The existence of distinct cell populations, 2) electrotonic influences of the surrounding atrium, 3) the presence of a high density of fibroblasts, and 4) atrial cells intermingled within the SAN. Our goal was to utilize a computer model to predict critical determinants and modulators of excitation and conduction in the SAN. We built a theoretical "non-uniform" model composed of distinct central and peripheral SAN cells and a "uniform" model containing only central cells connected to the atrium. We tested the effects of coupling strength between SAN cells in the models, as well as the effects of fibroblasts and interspersed atrial cells. Although we could simulate single cell experimental data supporting the "multiple cell type" hypothesis, 2D "non-uniform" models did not simulate expected tissue behavior, such as central pacemaking. When we considered the atrial effects alone in a simple homogeneous "uniform" model, central pacemaking initiation and impulse propagation in simulations were consistent with experiments. Introduction of fibroblasts in our simulated tissue resulted in various effects depending on the density, distribution, and fibroblast-myocyte coupling strength. Incorporation of atrial cells in our simulated SAN tissue had little effect on SAN electrophysiology. Our tissue model simulations suggest atrial electrotonic effects as plausible to account for SAN heterogeneity, sequence, and rate of propagation. Fibroblasts can act as obstacles, current sinks or shunts to conduction in the SAN depending on their orientation, density, and coupling.
窦房结(SAN)是一个复杂的结构,具有解剖学和功能异质性,这可能取决于:1)存在不同的细胞群体,2)周围心房的电紧张影响,3)存在高密度的成纤维细胞,以及 4)心房细胞混入 SAN 中。我们的目标是利用计算机模型来预测 SAN 中兴奋和传导的关键决定因素和调节剂。我们构建了一个理论上的“非均匀”模型,由不同的中央和周围 SAN 细胞组成,以及一个仅包含与心房相连的中央细胞的“均匀”模型。我们测试了模型中 SAN 细胞之间的耦合强度的影响,以及成纤维细胞和散布的心房细胞的影响。尽管我们可以模拟支持“多种细胞类型”假说的单个细胞实验数据,但 2D“非均匀”模型并没有模拟出预期的组织行为,例如中央起搏。当我们在一个简单的均匀“均匀”模型中单独考虑心房的影响时,中央起搏的起始和模拟中的冲动传播与实验一致。在我们模拟的组织中引入成纤维细胞会根据密度、分布和成纤维细胞-心肌细胞的耦合强度产生各种影响。在我们模拟的 SAN 组织中引入心房细胞对 SAN 电生理学几乎没有影响。我们的组织模型模拟表明,心房电紧张效应可能是 SAN 异质性、序列和传播速度的合理解释。成纤维细胞可以根据其方向、密度和耦合作用,在 SAN 中充当传导的障碍、电流汇或分流。