The relationship between cardiac endothelium and fibroblasts: it's complicated

被引:7
|
作者
Karra, Ravi [1 ,2 ]
Walter, Agoston O. [2 ]
Wu, Sean M. [3 ,4 ,5 ]
机构
[1] Duke Univ, Regenerat Next, Durham, NC 27710 USA
[2] Duke Univ, Dept Med, Durham, NC 27710 USA
[3] Stanford Univ, Cardiovasc Inst, Stanford, CA 94305 USA
[4] Stanford Univ, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Med, Div Cardiovasc Med, Stanford, CA 94305 USA
来源
JOURNAL OF CLINICAL INVESTIGATION | 2017年 / 127卷 / 08期
关键词
TRANSITION CONTRIBUTES; CORONARY-ARTERIES; FORM;
D O I
10.1172/JCI95492
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Coronary revascularization is an effective means of treating ischemic heart disease; however, current therapeutic revascularization strategies are limited to large caliber vessels. Because the mammalian heart scars following cardiac injury, recent work showing that cardiac fibroblasts can transdifferentiate into new coronary endothelium raises a new and exciting approach to promoting endogenous revascularization following cardiac injury. In this issue of the JCI, He et al. report on their employment of a battery of lineage-tracing tools to address the developmental origins of fibroblasts that give rise to new endothelial cells. Surprisingly, cardiac fibroblasts did not appear to contribute appreciably to regeneration of cardiac endothelium. Instead, cardiac endothelial cells were likely to proliferate and generate new endothelium following injury. As these conclusions diverge from prior findings, additional work will be required to understand the sources that generate cardiac endothelium in new blood vessels after injury. Clarification of the origins of coronary endothelial cells during cardiac repair is essential for identifying improved approaches to revascularizing damaged myocardium in patients with ischemic heart disease.
引用
收藏
页码:2892 / 2894
页数:3
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