a Department of Pathology and Laboratory Medicine, College of Medicine, University of Saskatchewan, Saskatoon, SK S7N 0W8, Canada.
Can J Physiol Pharmacol. 2013 Dec;91(12):985-98. doi: 10.1139/cjpp-2013-0161. Epub 2013 Aug 26.
The success of any work with isolated cardiomyocytes depends on the reproducibility of cell isolation, because the cells do not divide. To date, there is no suitable in vitro model to study human adult cardiac cell biology. Although embryonic stem cells and induced pluripotent stem cells are able to differentiate into cardiomyocytes in vitro, the efficiency of this process is low. Isolation and expansion of human cardiomyocyte progenitor cells from cardiac surgical waste or, alternatively, from fetal heart tissue is another option. However, to overcome various issues related to human tissue usage, especially ethical concerns, researchers use large- and small-animal models to study cardiac pathophysiology. A simple model to study the changes at the cellular level is cultures of cardiomyocytes. Although primary murine cardiomyocyte cultures have their own advantages and drawbacks, alternative strategies have been developed in the last two decades to minimise animal usage and interspecies differences. This review discusses the use of freshly isolated murine cardiomyocytes and cardiomyocyte alternatives for use in cardiac disease models and other related studies.
任何与分离的心肌细胞相关的工作的成功都取决于细胞分离的可重复性,因为细胞不会分裂。迄今为止,还没有合适的体外模型来研究人类成人心肌细胞生物学。尽管胚胎干细胞和诱导多能干细胞能够在体外分化为心肌细胞,但这一过程的效率很低。从心脏手术废物或替代地从胎儿心脏组织中分离和扩增人心肌细胞祖细胞是另一种选择。然而,为了克服与人类组织使用相关的各种问题,特别是伦理问题,研究人员使用大动物和小动物模型来研究心脏病理生理学。研究细胞水平变化的简单模型是心肌细胞培养。尽管原代鼠心肌细胞培养有其自身的优点和缺点,但在过去二十年中,已经开发出替代策略来最小化动物使用和种间差异。这篇综述讨论了新鲜分离的鼠心肌细胞和心肌细胞替代物在心脏疾病模型和其他相关研究中的应用。