Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430060, P.R. China.
Int J Mol Med. 2019 Feb;43(2):879-889. doi: 10.3892/ijmm.2018.4002. Epub 2018 Nov 27.
Hybrid approaches combining gene‑ and cell‑based therapies to make biological pacemakers are a promising therapeutic avenue for bradyarrhythmia. The present study aimed to direct adipose tissue‑derived stem cells (ADSCs) to differentiate specifically into cardiac pacemaker cells by overexpressing a single transcription factor, insulin gene enhancer binding protein 1 (ISL‑1). In the present study, the ADSCs were transfected with ISL‑1 or mCherry fluorescent protein lentiviral vectors and co‑cultured with neonatal rat ventricular cardiomyocytes (NRVMs) in vitro for 5‑7 days. The feasibility of regulating the differentiation of ADSCs into pacemaker‑like cells by overexpressing ISL‑1 was evaluated by observation of cell morphology and beating rate, reverse transcription‑quantitative polymerase chain reaction analysis, western blotting, immunofluorescence and analysis of electrophysiological activity. In conclusion, these data indicated that the overexpression of ISL‑1 in ADSCs may enhance the pacemaker phenotype and automaticity in vitro, features which were significantly increased following co‑culture induction.
将基因和细胞疗法相结合的杂交方法来制作生物起搏器,是治疗心动过缓的一种很有前途的治疗方法。本研究旨在通过过表达单个转录因子胰岛素基因增强结合蛋白 1(ISL-1),将脂肪组织来源的干细胞(ADSCs)定向分化为特定的心脏起搏细胞。在本研究中,ADSCs 被转染了 ISL-1 或 mCherry 荧光蛋白慢病毒载体,并与新生大鼠心室肌细胞(NRVMs)在体外共培养 5-7 天。通过观察细胞形态和搏动率、逆转录-定量聚合酶链反应分析、蛋白质印迹、免疫荧光和电生理活性分析,评估了过表达 ISL-1 调节 ADSC 分化为起搏样细胞的可行性。总之,这些数据表明,ISL-1 在 ADSC 中的过表达可能增强体外起搏表型和自动性,共培养诱导后这些特征显著增加。