Uygur Aysu, Lee Richard T
Department of Stem Cell and Regenerative Biology, Brigham Regenerative Medicine Center, Brigham and Women's Hospital, Harvard Medical School, Harvard University, Cambridge, MA 02139, USA; Harvard Stem Cell Institute, Cambridge, MA 02138, USA.
Department of Stem Cell and Regenerative Biology, Brigham Regenerative Medicine Center, Brigham and Women's Hospital, Harvard Medical School, Harvard University, Cambridge, MA 02139, USA; Harvard Stem Cell Institute, Cambridge, MA 02138, USA.
Dev Cell. 2016 Feb 22;36(4):362-74. doi: 10.1016/j.devcel.2016.01.018.
Adult humans fail to regenerate their hearts following injury, and this failure to regenerate myocardium is a leading cause of heart failure and death worldwide. Although all adult mammals appear to lack significant cardiac regeneration potential, some vertebrates can regenerate myocardium throughout life. In addition, new studies indicate that mammals have cardiac regeneration potential during development and very soon after birth. The mechanisms of heart regeneration among model organisms, including neonatal mice, appear remarkably similar. Orchestrated waves of inflammation, matrix deposition and remodeling, and cardiomyocyte proliferation are commonly seen in heart regeneration models. Understanding why adult mammals develop extensive scarring instead of regeneration is a crucial goal for regenerative biology.
成年人类心脏受伤后无法再生,心肌再生失败是全球心力衰竭和死亡的主要原因。尽管所有成年哺乳动物似乎都缺乏显著的心脏再生潜力,但一些脊椎动物一生都能再生心肌。此外,新研究表明,哺乳动物在发育期间和出生后不久具有心脏再生潜力。包括新生小鼠在内的模式生物的心脏再生机制似乎非常相似。在心脏再生模型中,通常会出现炎症、基质沉积和重塑以及心肌细胞增殖的协调浪潮。了解成年哺乳动物为何形成广泛瘢痕而非再生是再生生物学的一个关键目标。