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Arteries are formed by vein-derived endothelial tip cells

机译:动脉由静脉来源的内皮尖端细胞形成

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摘要

Tissue vascularization entails the formation of a blood vessel plexus, which remodels into arteries and veins. Here we show, by using time-lapse imaging of zebrafish fin regeneration and genetic lineage tracing of endothelial cells in the mouse retina, that vein-derived endothelial tip cells contribute to emerging arteries. Our movies uncover that arterial-fated tip cells change migration direction and migrate backwards within the expanding vascular plexus. This behaviour critically depends on chemokine receptor cxcr4a function. We show that the relevant Cxcr4a ligand Cxcl12a selectively accumulates in newly forming bone tissue even when ubiquitously overexpressed, pointing towards a tissue-intrinsic mode of chemokine gradient formation. Furthermore, we find that cxcr4a mutant cells can contribute to developing arteries when in association with wild-type cells, suggesting collective migration of endothelial cells. Together, our findings reveal specific cell migratory behaviours in the developing blood vessel plexus and uncover a conserved mode of artery formation.
机译:组织血管化需要形成血管丛,该血管丛会重塑成动脉和静脉。在这里,我们显示,通过使用斑马鱼鳍再生的延时成像和小鼠视网膜中内皮细胞的遗传谱系追踪,静脉源性内皮尖端细胞有助于新兴的动脉。我们的电影发现,动脉结扎的尖端细胞会在扩展的血管丛内改变迁移方向并向后迁移。这种行为严重取决于趋化因子受体cxcr4a的功能。我们表明相关的Cxcr4a配体Cxcl12a选择性地积累在新形成的骨组织中,即使普遍存在过表达时,也指向趋化因子梯度形成的组织本征模式。此外,我们发现cxcr4a突变细胞与野生型细胞结合时可促进动脉发育,提示内皮细胞的集体迁移。在一起,我们的发现揭示了发展中的血管丛中特定的细胞迁移行为,并揭示了一种保守的动脉形成方式。

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