Cai Jun, Lin Guosheng, Jiang Hong, Yang Bo, Jiang Xuejun, Yu Qijing, Song Jian
Department of Cardiology, Renmin Hospital of Wuhan University, PR China.
Transplantation. 2006 Apr 15;81(7):1022-6. doi: 10.1097/01.tp.0000214954.09515.51.
Sinus node dysfunction and severe heart block are major indications for electronic pacemaker implantation. The aim of the present study was to investigate the feasibility of an alternative approach by using spontaneously excitable cell grafts to serve as a biological pacemaker.
Enzymatically isolated neonatal atrial cardiomyocytes (including sinus nodal cells) were grafted into the free wall of the left ventricle of 5 male pigs. In the control group (n = 4), the medium was used for injecting. Three weeks after the transplantation the pigs underwent catheter ablation of the atrioventricular (AV) node. Microelectrode technique was used to record the transmembrane action potential of myocytes from cell- and medium-injected preparations. Immunohistochemistry was used to verify the grafted cells and the establishment of the gap junctions between donor and host cardiomyocytes.
After the creation of complete AV-block, a higher average idioventricular rate was observed in cell-grafted pigs than that in control pigs (89 +/- 13 vs. 30 +/- 11 bpm, P < 0.05). Administering isoprenaline caused a significant increase in the idioventricular rate from 89 +/- 13 to 120 +/- 18 bpm in the cell-grafted animals (P < 0.05). Microelectrode recordings showed that the spontaneously beating rate was significantly higher in the cell-implanted than that in the control preparations (82 +/- 17 vs. 33 +/- 13 bpm, P < 0.05). Furthermore, the immunofluorescence microscopy identified the DAPI-labeled donor cells, and the connexin-43 and N-cadherin positive junctions between them and host cardiomyocytes.
Grafted neonatal atrial cardiomyocytes are able to survive and integrate into the host myocardium, and show a pacing function that can be modulated by autonomic agents.
窦房结功能障碍和严重心脏传导阻滞是电子起搏器植入的主要适应症。本研究的目的是探讨使用自发兴奋性细胞移植作为生物起搏器的替代方法的可行性。
将酶分离的新生心房心肌细胞(包括窦房结细胞)移植到5只雄性猪的左心室游离壁。对照组(n = 4)注射培养基。移植三周后,对猪进行房室结导管消融。采用微电极技术记录细胞注射组和培养基注射组心肌细胞的跨膜动作电位。免疫组织化学用于验证移植细胞以及供体和宿主心肌细胞之间缝隙连接的建立。
完全性房室传导阻滞形成后,细胞移植猪的平均心室自主节律高于对照组猪(89±13对30±11次/分,P<0.05)。在细胞移植动物中,给予异丙肾上腺素使心室自主节律从89±13显著增加至120±18次/分(P<0.05)。微电极记录显示,细胞植入组的自发搏动率显著高于对照组(82±17对33±13次/分,P<0.05)。此外,免疫荧光显微镜鉴定出DAPI标记的供体细胞,以及它们与宿主心肌细胞之间的连接蛋白43和N-钙黏蛋白阳性连接。
移植的新生心房心肌细胞能够存活并整合到宿主心肌中,并表现出可被自主神经药物调节的起搏功能。