动脉
生物
再生(生物学)
冠状动脉
内科学
侧支循环
动脉发生
心脏病学
抵押品
心脏病
缺血
医学
细胞生物学
财务
经济
作者
Soumyashree Das,Andrew Brooks Goldstone,Hanjay Wang,Justin M. Farry,Gaetano D’Amato,Michael J. Paulsen,Anahita Eskandari,Camille E. Hironaka,Ragini Phansalkar,Bikram Sharma,Siyeon Rhee,Elya Ali Shamskhou,Dritan Agalliu,Vinicio de Jesús Pérez,Yi-Ping Joseph Woo,Kristy Red‐Horse
出处
期刊:Cell
[Cell Press]
日期:2019-01-25
卷期号:176 (5): 1128-1142.e18
被引量:219
标识
DOI:10.1016/j.cell.2018.12.023
摘要
Collateral arteries are an uncommon vessel subtype that can provide alternate blood flow to preserve tissue following vascular occlusion. Some patients with heart disease develop collateral coronary arteries, and this correlates with increased survival. However, it is not known how these collaterals develop or how to stimulate them. We demonstrate that neonatal mouse hearts use a novel mechanism to build collateral arteries in response to injury. Arterial endothelial cells (ECs) migrated away from arteries along existing capillaries and reassembled into collateral arteries, which we termed “artery reassembly”. Artery ECs expressed CXCR4, and following injury, capillary ECs induced its ligand, CXCL12. CXCL12 or CXCR4 deletion impaired collateral artery formation and neonatal heart regeneration. Artery reassembly was nearly absent in adults but was induced by exogenous CXCL12. Thus, understanding neonatal regenerative mechanisms can identify pathways that restore these processes in adults and identify potentially translatable therapeutic strategies for ischemic heart disease.
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