心脏病
再生(生物学)
心力衰竭
医学
心脏发育
心脏病学
重症监护医学
内科学
生物
胚胎干细胞
生物化学
细胞生物学
基因
作者
Francisco X. Galdos,Yuxuan Guo,Sharon L. Paige,Nathan J. VanDusen,Sean M. Wu,William T. Pu
出处
期刊:Circulation Research
[Ovid Technologies (Wolters Kluwer)]
日期:2017-03-16
卷期号:120 (6): 941-959
被引量:134
标识
DOI:10.1161/circresaha.116.309040
摘要
Palliative surgery for congenital heart disease has allowed patients with previously lethal heart malformations to survive and, in most cases, to thrive. However, these procedures often place pressure and volume loads on the heart, and over time, these chronic loads can cause heart failure. Current therapeutic options for initial surgery and chronic heart failure that results from failed palliation are limited, in part, by the mammalian heart’s low inherent capacity to form new cardiomyocytes. Surmounting the heart regeneration barrier would transform the treatment of congenital, as well as acquired, heart disease and likewise would enable development of personalized, in vitro cardiac disease models. Although these remain distant goals, studies of heart development are illuminating the path forward and suggest unique opportunities for heart regeneration, particularly in fetal and neonatal periods. Here, we review major lessons from heart development that inform current and future studies directed at enhancing cardiac regeneration.
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