Hasan Sana S, Tsaryk Roman, Lange Martin, Wisniewski Laura, Moore John C, Lawson Nathan D, Wojciechowska Karolina, Schnittler Hans, Siekmann Arndt F
Max Planck Institute for Molecular Biomedicine, Röntgenstrasse 20, D-48149 Münster, Germany.
Cells-in-Motion Cluster of Excellence (EXC 1003 - CiM), University of Muenster, D-48149 Muenster, Germany.
Nat Cell Biol. 2017 Aug;19(8):928-940. doi: 10.1038/ncb3574. Epub 2017 Jul 17.
Angiogenic sprouting needs to be tightly controlled. It has been suggested that the Notch ligand dll4 expressed in leading tip cells restricts angiogenesis by activating Notch signalling in trailing stalk cells. Here, we show using live imaging in zebrafish that activation of Notch signalling is rather required in tip cells. Notch activation initially triggers expression of the chemokine receptor cxcr4a. This allows for proper tip cell migration and connection to the pre-existing arterial circulation, ultimately establishing functional arterial-venous blood flow patterns. Subsequently, Notch signalling reduces cxcr4a expression, thereby preventing excessive blood vessel growth. Finally, we find that Notch signalling is dispensable for limiting blood vessel growth during venous plexus formation that does not generate arteries. Together, these findings link the role of Notch signalling in limiting angiogenesis to its role during artery formation and provide a framework for our understanding of the mechanisms underlying blood vessel network expansion and maturation.
血管生成芽需要受到严格控制。有人提出,在前端细胞中表达的Notch配体dll4通过激活后端柄细胞中的Notch信号来限制血管生成。在这里,我们利用斑马鱼的活体成像显示,Notch信号的激活在前端细胞中是必需的。Notch激活最初触发趋化因子受体cxcr4a的表达。这使得前端细胞能够正常迁移并与预先存在的动脉循环相连,最终建立起功能性的动静脉血流模式。随后,Notch信号降低cxcr4a的表达,从而防止血管过度生长。最后,我们发现Notch信号对于在不产生动脉的静脉丛形成过程中限制血管生长是可有可无的。总之,这些发现将Notch信号在限制血管生成中的作用与其在动脉形成过程中的作用联系起来,并为我们理解血管网络扩张和成熟的潜在机制提供了一个框架。