Nakanishi Hiroyuki, Lee Jong-Kook, Miwa Keiko, Masuyama Kiyoshi, Yasutake Hideki, Li Jun, Tomoyama Satoki, Honda Yayoi, Deguchi Jiro, Tsujimoto Shinji, Hidaka Kyoko, Miyagawa Shigeru, Sawa Yoshiki, Komuro Issei, Sakata Yasushi
Department of Cardiovascular Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Department of Advanced Cardiovascular Regenerative Medicine, Graduate School of Medicine, Osaka University, Suita, Japan.
Front Physiol. 2019 Jun 27;10:818. doi: 10.3389/fphys.2019.00818. eCollection 2019.
Ectopic foci from pulmonary veins (PVs) comprise the main trigger associated with the initiation of atrial fibrillation (AF). An abrupt anatomical narrow-to-wide transition, modeled as geometrical patterning with similar configuration in the present study, is located at the junction of PVs and the left atrium (LA). Complex cellular composition, i.e., constituent cell heterogeneity, is also observed in PVs and the PVs-LA junction. High frequency triggers accompanied with anatomical irregularity and constituent cell heterogeneity provoke impaired conduction, a prerequisite for AF genesis. However, few experiments investigating the effects of these factors on electrophysiological properties using human-based cardiomyocytes (CMs) with atrial properties have been reported. The aim of the current study was to estimate whether geometrical patterning and constituent cell heterogeneity under high frequency stimuli undergo conduction disturbance utilizing an two-dimensional (2D) monolayer preparation consisting of atrial-like CMs derived from human induced pluripotent stem cells (hiPSCs) and atrial fibroblasts (Fbs). We induced hiPSCs into atrial-like CMs using a directed cardiac differentiation protocol with the addition of all- retinoic acid (ATRA). The atrial-like hiPSC-derived CMs (hiPSC-CMs) and atrial Fbs were transferred in defined ratios (CMs/Fbs: 100%/0% or 70%/30%) on manually fabricated plates with or without geometrical patterning imitating the PVs-LA junction. High frequency field stimulation emulating repetitive ectopic foci originated in PVs were delivered, and the electrical propagation was assessed by optical mapping. We generated high purity CMs with or without the ATRA application. ATRA-treated hiPSC-CMs exhibited significantly higher atrial-specific properties by immunofluorescence staining, gene expression patterns, and optical action potential parameters than those of ATRA-untreated hiPSC-CMs. Electrical stimuli at a higher frequency preferentially induced impaired electrical conduction on atrial-like hiPSC-CMs monolayer preparations with an abrupt geometrical transition than on those with uniform geometry. Additionally, the application of human atrial Fbs to the geometrically patterned atrial-like hiPSC-CMs tended to further deteriorate the integrity of electrical conduction compared with those using the atrial-like hiPSC-CM alone preparations. Thus, geometrical narrow-to-wide patterning under high frequency stimuli preferentially jeopardized electrical conduction within atrial-like hiPSC-CM monolayers. Constituent cell heterogeneity represented by atrial Fbs also contributed to the further deterioration of conduction stability.
肺静脉(PVs)的异位灶是与心房颤动(AF)起始相关的主要触发因素。在本研究中,将其建模为具有相似构型的几何图案,在PVs与左心房(LA)的交界处存在从狭窄到宽阔的突然解剖学转变。在PVs和PVs - LA交界处也观察到复杂的细胞组成,即组成细胞的异质性。伴有解剖学不规则和组成细胞异质性的高频触发因素会引发传导受损,这是AF发生的一个先决条件。然而,很少有实验报道使用具有心房特性的人源性心肌细胞(CMs)来研究这些因素对电生理特性的影响。本研究的目的是利用由源自人诱导多能干细胞(hiPSCs)的心房样CMs和心房成纤维细胞(Fbs)组成的二维(2D)单层制剂,评估在高频刺激下几何图案和组成细胞异质性是否会导致传导紊乱。我们使用添加了全反式维甲酸(ATRA)的定向心脏分化方案将hiPSCs诱导为心房样CMs。将心房样hiPSC衍生的CMs(hiPSC - CMs)和心房Fbs按确定的比例(CMs/Fbs:100%/0%或70%/30%)转移到人工制作的、具有或不具有模仿PVs - LA交界处几何图案的平板上。施加模拟起源于PVs的重复性异位灶的高频电场刺激,并通过光学标测评估电传播。我们在应用或不应用ATRA的情况下生成了高纯度的CMs。通过免疫荧光染色、基因表达模式和光学动作电位参数,ATRA处理的hiPSC - CMs表现出比未处理的hiPSC - CMs显著更高的心房特异性特性。与具有均匀几何形状的制剂相比,较高频率的电刺激优先在具有突然几何转变的心房样hiPSC - CMs单层制剂上诱导电传导受损。此外,与单独使用心房样hiPSC - CM制剂相比,将人心房Fbs应用于具有几何图案的心房样hiPSC - CMs往往会进一步破坏电传导的完整性。因此,在高频刺激下从狭窄到宽阔的几何图案优先危及心房样hiPSC - CM单层内的电传导。由心房Fbs代表的组成细胞异质性也导致传导稳定性进一步恶化。