抵押品
侧支循环
心脏病学
内科学
动脉
动脉发生
冠状动脉
医学
转录因子
生物
内皮
内皮干细胞
追踪
细胞生物学
细胞谱系
机制(生物学)
赫斯1
冠状动脉循环
血管生成
作者
Mingjun Zhang,Maoying Han,Yangfeng Hou,Zixin Liu,Yilian Wang,Xiuzhen Huang,Cheng Kiu Ho,Hang Qu,Qing‐Dong Wang,Xin Ma,Kathy O. Lui,Bin Zhou
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-08-20
卷期号:393 (6813)
标识
DOI:10.1126/science.ady3027
摘要
Coronary collateral arteries have been proposed to form de novo through artery reassembly, a process in which arterial endothelial cells (ECs) migrate away from preexisting arteries and reassemble into new arteries. Using genetic tools that trace arterial ECs, we found that their contribution to collaterals is modest. Dual genetic lineage tracing revealed that capillary ECs, rather than arterial ECs, serve as the major building blocks for de novo collaterals. The capillary-to-collateral conversion is functionally crucial for cardiac repair. In addition, transient Vegfa expression through modified messenger RNA markedly promoted collateral formation. Mechanistically, vascular endothelial growth factor (VEGF) drives arterialization by regulating HES1 transcription through YY1/SETD1A-mediated H3K4 trimethylation. Collectively, these findings redefine the cellular origin and mechanism of coronary collateral formation and highlight its role in facilitating efficient cardiac repair.
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