Laboratory of Cardiovascular Science, Biomedical Research Center, National Institute on Aging, National Institutes of Health , Baltimore, Maryland.
Department of Cardiovascular Electrophysiology, The Johns Hopkins Hospital , Baltimore, Maryland.
Am J Physiol Heart Circ Physiol. 2018 Mar 1;314(3):H403-H414. doi: 10.1152/ajpheart.00253.2016. Epub 2017 Sep 15.
Cardiac pacemaker cells, including cells of the sinoatrial node, are heterogeneous in size, morphology, and electrophysiological characteristics. The exact extent to which these cells differ electrophysiologically is unclear yet is critical to understanding their functioning. We examined major ionic currents in individual intercaval pacemaker cells (IPCs) sampled from the paracristal, intercaval region (including the sinoatrial node) that were spontaneously beating after enzymatic isolation from rabbit hearts. The beating rate was measured at baseline and after inhibition of the Ca pump with cyclopiazonic acid. Thereafter, in each cell, we consecutively measured the density of funny current ( I), delayed rectifier K current ( I) (a surrogate of repolarization capacity), and L-type Ca current ( I) using whole cell patch clamp The ionic current densities varied to a greater extent than previously appreciated, with some IPCs demonstrating very small or zero I . The density of none of the currents was correlated with cell size, while I and I densities were related to baseline beating rates. I density was correlated with I density but not with that of I. Inhibition of Ca cycling had a greater beating rate slowing effect in IPCs with lower I densities. Our numerical model simulation indicated that 1) IPCs with small (or zero) I or small I can operate via a major contribution of Ca clock, 2) I-Ca-clock interplay could be important for robust pacemaking function, and 3) coupled I- I function could regulate maximum diastolic potential. Thus, we have demonstrated marked electrophysiological heterogeneity of IPCs. This heterogeneity is manifested in basal beating rate and response to interference of Ca cycling, which is linked to I. NEW & NOTEWORTHY In the present study, a hitherto unrecognized range of heterogeneity of ion currents in pacemaker cells from the intercaval region is demonstrated. Relationships between basal beating rate and L-type Ca current and funny current ( I) density are uncovered, along with a positive relationship between I and delayed rectifier K current. Links are shown between the response to Ca cycling blockade and I density.
心脏起搏器细胞,包括窦房结细胞,在大小、形态和电生理特征上存在异质性。这些细胞在电生理上的差异程度尚不清楚,但对理解它们的功能至关重要。我们检查了从兔心中酶解分离后自发跳动的冠状窦起搏细胞(IPCs)中单个细胞的主要离子电流。在使用全细胞膜片钳技术测量时,首先在基础状态下测量起搏率,然后用环匹阿尼酸抑制钙泵。此后,在每个细胞中,我们依次测量了有趣电流(I)、延迟整流钾电流(I)(复极化能力的替代物)和 L 型钙电流(I)的密度。离子电流密度的变化程度大于以前的认识,一些 IPC 表现出非常小或零的 I。没有一种电流的密度与细胞大小相关,而 I 和 I 的密度与基础起搏率相关。I 密度与 I 密度相关,但与 I 密度不相关。钙循环抑制在 IPC 中具有较低的 I 密度时对起搏率的减慢作用更大。我们的数值模型模拟表明:1)具有较小(或为零)I 或较小 I 的 IPC 可以通过钙钟的主要贡献来运行;2)I-Ca 钟相互作用对稳健的起搏功能可能很重要;3)偶联的 I- I 功能可以调节最大舒张电位。因此,我们已经证明了 IPC 具有显著的电生理异质性。这种异质性表现在基础起搏率和钙循环干扰的反应上,这与 I 有关。新的和值得注意的是,在本研究中,证明了窦房结区起搏细胞离子电流的一种前所未有的异质性范围。揭示了基础起搏率与 L 型钙电流和有趣电流(I)密度之间的关系,以及 I 与延迟整流钾电流之间的正相关关系。还显示了钙循环阻断与 I 密度之间的关系。