Department of Biology, Stanford University, Stanford, CA 94305, USA.
Department of Cardiothoracic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.
Cell. 2019 Feb 21;176(5):1128-1142.e18. doi: 10.1016/j.cell.2018.12.023. Epub 2019 Jan 24.
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.
侧支血管是一种不常见的血管亚型,可在血管阻塞后提供替代血流以维持组织。一些患有心脏病的患者会发展出侧支冠状动脉,这与存活率的提高相关。然而,目前尚不清楚这些侧支血管是如何形成的,也不知道如何刺激它们。我们证明,新生小鼠心脏使用一种新的机制来应对损伤建立侧支血管。动脉内皮细胞(EC)沿着现有的毛细血管从动脉迁移,并重新组装成侧支血管,我们称之为“动脉重排”。动脉 EC 表达 CXCR4,损伤后,毛细血管 EC 诱导其配体 CXCL12。CXCL12 或 CXCR4 的缺失会损害侧支动脉的形成和新生心脏的再生。成人中几乎没有动脉重排,但外源性 CXCL12 可诱导其产生。因此,了解新生儿的再生机制可以确定在成人中恢复这些过程的途径,并为缺血性心脏病确定潜在可转化的治疗策略。