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Notch promotes vascular maturation by inducing integrin-mediated smooth muscle cell adhesion to the endothelial basement membrane

机译:Notch通过诱导整合素介导的平滑肌细胞粘附于内皮基底膜来促进血管成熟

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摘要

Vascular development and angiogenesis initially depend on endothelial tip cell invasion, which is followed by a series of maturation steps, including lumen formation and recruitment of perivascular cells. Notch ligands expressed on the endothelium and their cognate receptors expressed on perivascular cells are involved in blood vessel maturation, though little is known regarding the Notchdependent effectors that facilitate perivascular coverage of nascent vessels. Here, we report that vascular smooth muscle cell (VSMC) recognition of the Notch ligand Jagged1 on endothelial cells leads to expression of integrin αvβ3 on VSMCs. Once expressed, integrin αvβ3 facilitates VSMC adhesion to VWF in the endothelial basement membrane of developing retinal arteries, leading to vessel maturation. Genetic or pharmacologic disruption of Jagged1, Notch, αvβ3, or VWF suppresses VSMC coverage of nascent vessels and arterial maturation during vascular development. Therefore, we define a Notch-mediated interaction between the developing endothelium and VSMCs leading to adhesion of VSMCs to the endothelial basement membrane and arterial maturation.
机译:血管发育和血管生成最初取决于内皮尖端细胞的侵袭,随后是一系列成熟步骤,包括管腔形成和血管周细胞募集。在内皮中表达的Notch配体及其在血管周细胞上表达的同源受体与血管成熟有关,尽管对于促进新生血管的血管周覆盖的Notchdependent效应子知之甚少。在这里,我们报告血管平滑肌细胞(VSMC)识别内皮细胞上的Notch配体Jagged1导致VSMCs上整合素αvβ3的表达。一旦表达,整联蛋白αvβ3促进VSMC粘附在发育中的视网膜动脉内皮基底膜中的VWF上,从而导致血管成熟。 Jagged1,Notch,αvβ3或VWF的遗传或药理学破坏可抑制新生血管的VSMC覆盖和血管发育过程中的动脉成熟。因此,我们定义了由Notch介导的内皮与VSMC之间的相互作用,从而导致VSMC与内皮基底膜的粘附和动脉成熟。

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