Watanabe Tatsuya, Hatayama Naoyuki, Guo Marissa, Yuhara Satoshi, Shinoka Toshiharu
Center for Regenerative Medicine, The Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH 43205, USA.
Department of Anatomy, Aichi Medical University, Nagakute 480-1195, Japan.
Bioengineering (Basel). 2024 Sep 24;11(10):954. doi: 10.3390/bioengineering11100954.
Cardiovascular diseases, particularly ischemic heart disease, area leading cause of morbidity and mortality worldwide. Myocardial infarction (MI) results in extensive cardiomyocyte loss, inflammation, extracellular matrix (ECM) degradation, fibrosis, and ultimately, adverse ventricular remodeling associated with impaired heart function. While heart transplantation is the only definitive treatment for end-stage heart failure, donor organ scarcity necessitates the development of alternative therapies. In such cases, methods to promote endogenous tissue regeneration by stimulating growth factor secretion and vascular formation alone are insufficient. Techniques for the creation and transplantation of viable tissues are therefore highly sought after. Approaches to cardiac regeneration range from stem cell injections to epicardial patches and interposition grafts. While numerous preclinical trials have demonstrated the positive effects of tissue transplantation on vasculogenesis and functional recovery, long-term graft survival in large animal models is rare. Adequate vascularization is essential for the survival of transplanted tissues, yet pre-formed microvasculature often fails to achieve sufficient engraftment. Recent studies report success in enhancing cell survival rates in vitro via tissue perfusion. However, the transition of these techniques to in vivo models remains challenging, especially in large animals. This review aims to highlight the evolution of cardiac patch and stem cell therapies for the treatment of cardiovascular disease, identify discrepancies between in vitro and in vivo studies, and discuss critical factors for establishing effective myocardial tissue regeneration in vivo.
心血管疾病,尤其是缺血性心脏病,是全球发病和死亡的主要原因。心肌梗死(MI)会导致大量心肌细胞丧失、炎症、细胞外基质(ECM)降解、纤维化,最终导致与心脏功能受损相关的不良心室重塑。虽然心脏移植是终末期心力衰竭的唯一确定性治疗方法,但供体器官稀缺使得开发替代疗法成为必要。在这种情况下,仅通过刺激生长因子分泌和血管形成来促进内源性组织再生的方法是不够的。因此,用于创建和移植有活力组织的技术备受追捧。心脏再生的方法从干细胞注射到心外膜贴片和介入移植物不等。虽然众多临床前试验已经证明了组织移植对血管生成和功能恢复的积极作用,但在大型动物模型中长期移植物存活情况罕见。充足的血管化对于移植组织的存活至关重要,然而预先形成的微脉管系统往往无法实现足够的植入。最近的研究报告了通过组织灌注提高体外细胞存活率方面取得的成功。然而,将这些技术转化为体内模型仍然具有挑战性,尤其是在大型动物中。本综述旨在突出用于治疗心血管疾病的心脏贴片和干细胞疗法的发展历程,识别体外和体内研究之间的差异,并讨论在体内建立有效的心肌组织再生的关键因素。