Department of Cell and Developmental Biology, Institute of Zoology (ZOO), Karlsruhe Institute of Technology (KIT), Fritz Haber Weg 4, 76131, Karlsruhe, Germany.
Institute for Biological and Chemical Systems-Biological Information Processing, Karlsruhe Institute of Technology (KIT), PO Box 3640, 76021, Karlsruhe, Germany.
Nat Commun. 2024 Apr 10;15(1):3118. doi: 10.1038/s41467-024-47434-x.
Formation of organo-typical vascular networks requires cross-talk between differentiating parenchymal cells and developing blood vessels. Here we identify a Vegfa driven venous sprouting process involving parenchymal to vein cross-talk regulating venous endothelial Vegfa signaling strength and subsequent formation of a specialized angiogenic cell, prefabricated with an intact lumen and pericyte coverage, termed L-Tip cell. L-Tip cell selection in the venous domain requires genetic interaction between vascular Aplnra and Kdrl in a subset of venous endothelial cells and exposure to parenchymal derived Vegfa and Apelin. Parenchymal Esm1 controls the spatial positioning of venous sprouting by fine-tuning local Vegfa availability. These findings may provide a conceptual framework for understanding how Vegfa generates organo-typical vascular networks based on the selection of competent endothelial cells, induced via spatio-temporal control of endothelial Kdrl signaling strength involving multiple parenchymal derived cues generated in a tissue dependent metabolic context.
器官特化血管网络的形成需要分化实质细胞和发育中的血管之间的串扰。在这里,我们确定了一个由 Vegfa 驱动的静脉发芽过程,涉及实质到静脉的串扰,调节静脉内皮细胞 Vegfa 信号强度,随后形成一个专门的血管生成细胞,预先形成完整的管腔和周细胞覆盖,称为 L-Tip 细胞。L-Tip 细胞在静脉区域的选择需要血管 Aplnra 和 Kdrl 在静脉内皮细胞中的亚群之间的遗传相互作用,以及暴露于实质来源的 Vegfa 和 Apelin。实质 Esm1 通过精细调节局部 Vegfa 的可用性来控制静脉发芽的空间定位。这些发现可能为理解 Vegfa 如何基于对有能力的内皮细胞的选择生成器官特化血管网络提供一个概念框架,这种选择是通过涉及在组织依赖的代谢背景中生成的多个实质来源的线索的内皮细胞 Kdrl 信号强度的时空控制来诱导的。