Jin Chunna, Zhu Shiyu, Zhao Tingting, Deng Jiewen, Xiang Meixiang, Ma Hong
Department of Cardiology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Ann Transl Med. 2022 Nov;10(21):1179. doi: 10.21037/atm-22-2649.
Cardiovascular diseases have been the leading cause of death globally for decades. Pharmacological advances targeting the sympathetic nervous system, renin-angiotensin-aldosterone system, and fibrosis slow the progression of diverse cardiovascular diseases. However, ongoing cardiomyocyte loss is inevitable in divergent cardiovascular diseases, eventually leading to heart failure as the end stage. In this review, we focused on the key biomedical findings and underlying principles of cardiomyocyte regeneration.
Literature regarding the key findings in cardiomyocyte regeneration research, including controversies on the origins of newly formed cardiomyocytes, potential barriers and strategies to heart regeneration, and the key animals, models, and methods applied in the study of heart regeneration, were broadly researched using the PubMed and Web of Science databases.
In the mammalian heart, cardiomyocytes proliferate during the embryonic and early postnatal stages, while the capability of proliferation disappears in the adult stage. An increasing amount of evidence suggests that cardiomyocytes self-renew at a very limited level and that most newly formed cardiomyocytes originate from pre-existing cardiomyocytes and not cardiac progenitor cells (CPCs). Several potential barriers to heart regeneration have been addressed, including metabolic switch, a large increase in multinucleated and polyploid cardiomyocytes, and alteration in the epigenome and transcriptome. In addition, immune system evolution is also associated with the loss of regenerative capacity. However, the activation of resident cardiomyocytes, somatic cell reprogramming, and direct reprogramming, in addition to the promotion of neovascularization and immune modulation, constitute the new insights into those strategies that can boost cardiac regeneration.
Heart regeneration is one of the most popular fields in cardiovascular research and represents a promising avenue of therapeutics for mending a broken heart. Despite the controversies and challenges, a clearer picture of adult mammalian cardiac regeneration is emerging.
几十年来,心血管疾病一直是全球主要的死亡原因。针对交感神经系统、肾素 - 血管紧张素 - 醛固酮系统和纤维化的药理学进展减缓了多种心血管疾病的进展。然而,在各种心血管疾病中,心肌细胞持续丢失是不可避免的,最终导致心力衰竭这一终末期。在本综述中,我们聚焦于心肌细胞再生的关键生物医学发现及潜在机制。
利用PubMed和Web of Science数据库广泛检索了有关心肌细胞再生研究关键发现的文献,包括新形成心肌细胞的起源争议、心脏再生的潜在障碍和策略,以及心脏再生研究中应用的关键动物、模型和方法。
在哺乳动物心脏中,心肌细胞在胚胎期和出生后早期阶段增殖,而成年期增殖能力消失。越来越多的证据表明,心肌细胞在非常有限的水平上自我更新,并且大多数新形成的心肌细胞源自已有的心肌细胞,而非心脏祖细胞(CPCs)。已经探讨了心脏再生的几个潜在障碍,包括代谢转换、多核和多倍体心肌细胞大量增加以及表观基因组和转录组的改变。此外,免疫系统进化也与再生能力丧失有关。然而,除了促进新生血管形成和免疫调节外,驻留心肌细胞的激活、体细胞重编程和直接重编程构成了促进心脏再生策略的新见解。
心脏再生是心血管研究中最热门的领域之一,是修复受损心脏的一条有前景的治疗途径。尽管存在争议和挑战,但成年哺乳动物心脏再生的图景正在变得更加清晰。