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Notch配体Delta样蛋白4负向调节内皮尖端细胞形成和血管分支。

The Notch ligand Delta-like 4 negatively regulates endothelial tip cell formation and vessel branching.

作者信息

Suchting Steven, Freitas Catarina, le Noble Ferdinand, Benedito Rui, Bréant Christiane, Duarte Antonio, Eichmann Anne

机构信息

Institut National de la Santé et de la Recherche Médicale, U833, 75005 Paris, France.

出版信息

Proc Natl Acad Sci U S A. 2007 Feb 27;104(9):3225-30. doi: 10.1073/pnas.0611177104. Epub 2007 Feb 12.

Abstract

Delta-like 4 (Dll4) is a transmembrane ligand for Notch receptors that is expressed in arterial blood vessels and sprouting endothelial cells. Here we show that Dll4 regulates vessel branching during development by inhibiting endothelial tip cell formation. Heterozygous deletion of dll4 or pharmacological inhibition of Notch signaling using gamma-secretase inhibitor revealed a striking vascular phenotype, with greatly increased numbers of filopodia-extending endothelial tip cells and increased expression of tip cell marker genes compared with controls. Filopodia extension in dll4(+/-) retinal vessels required the vascular growth factor VEGF and was inhibited when VEGF signaling was blocked. Although VEGF expression was not significantly altered in dll4(+/-) retinas, dll4(+/-) vessels showed increased expression of VEGF receptor 2 and decreased expression of VEGF receptor 1 compared with wild-type, suggesting they could be more responsive to VEGF stimulation. In addition, expression of dll4 in wild-type tip cells was itself decreased when VEGF signaling was blocked, indicating that dll4 may act downstream of VEGF as a "brake" on VEGF-mediated angiogenic sprouting. Taken together, these data reveal Dll4 as a negative regulator of vascular sprouting and vessel branching that is required for normal vascular network formation during development.

摘要

Delta样4(Dll4)是Notch受体的跨膜配体,在动脉血管和正在发芽的内皮细胞中表达。我们在此表明,Dll4通过抑制内皮尖端细胞形成来调节发育过程中的血管分支。dll4的杂合缺失或使用γ-分泌酶抑制剂对Notch信号进行药理学抑制,均揭示出一种显著的血管表型,与对照组相比,伸出丝状伪足的内皮尖端细胞数量大幅增加,且尖端细胞标记基因的表达也有所增加。dll4(+/-)视网膜血管中的丝状伪足延伸需要血管生长因子VEGF,当VEGF信号被阻断时则受到抑制。尽管dll4(+/-)视网膜中的VEGF表达没有显著改变,但与野生型相比,dll4(+/-)血管中VEGF受体2的表达增加,而VEGF受体1的表达减少,这表明它们可能对VEGF刺激更敏感。此外,当VEGF信号被阻断时,野生型尖端细胞中dll4的表达本身也会降低,这表明dll4可能作为VEGF介导的血管生成发芽的“刹车”,作用于VEGF的下游。综上所述,这些数据揭示Dll4是血管发芽和血管分支的负调节因子,是发育过程中正常血管网络形成所必需的。

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