Eisenberg Leonard M, Eisenberg Carol A
Department of Cell Biology and Anatomy, Medical University of South Carolina, Charleston, South Carolina 29425, USA.
Anat Rec A Discov Mol Cell Evol Biol. 2004 Jan;276(1):103-12. doi: 10.1002/ar.a.10137.
Adult cardiac muscle is unable to repair itself following severe disease or injury. Because of this fundamental property of the myocardium, it was long believed that the adult myocardium is a postmitotic tissue. Yet, recent studies have indicated that new cardiac myocytes are generated throughout the life span of an adult and that extracardiac cells can contribute to the renewal of individual cells within the myocardium. In addition, investigations of the phenotypic capacity of adult stem cells have suggested that their potential is not solely restricted to the differentiated cell phenotypes of the source tissue. These observations have great implications for cardiac biology, as stem cells obtained from the bone marrow and other readily accessible adult tissues may serve as a source of replacement cardiac myocytes. In this review, we describe the evidence for these new findings and discuss their implications in context of the continuing controversy over stem cell plasticity.
成年心肌在遭受严重疾病或损伤后无法自我修复。由于心肌的这一基本特性,长期以来人们一直认为成年心肌是一种有丝分裂后组织。然而,最近的研究表明,成年个体在其整个生命周期中都会产生新的心肌细胞,并且心外细胞可以促进心肌内单个细胞的更新。此外,对成体干细胞表型能力的研究表明,它们的潜能并不局限于来源组织的分化细胞表型。这些观察结果对心脏生物学具有重要意义,因为从骨髓和其他易于获取的成年组织中获得的干细胞可能成为替代心肌细胞的来源。在这篇综述中,我们描述了这些新发现的证据,并在关于干细胞可塑性的持续争论背景下讨论了它们的意义。