Duarte António, Hirashima Masanori, Benedito Rui, Trindade Alexandre, Diniz Patrícia, Bekman Evguenia, Costa Luís, Henrique Domingos, Rossant Janet
CIISA, Faculdade de Medicina Veterinária, 1300-0-477 Lisboa, Portugal.
Genes Dev. 2004 Oct 15;18(20):2474-8. doi: 10.1101/gad.1239004. Epub 2004 Oct 1.
Involvement of the Notch signaling pathway in vascular development has been demonstrated by both gain- and loss-of-function mutations in humans, mice, and zebrafish. In zebrafish, Notch signaling is required for arterial identity by suppressing the venous fate in developing artery cells. In mice, the Notch4 receptor and the Delta-like 4 (Dll4) ligand are specifically expressed in arterial endothelial cells, suggesting a similar role. Here we show that the Dll4 ligand alone is required in a dosage-sensitive manner for normal arterial patterning in development. This implicates Dll4 as the specific mammalian endothelial ligand for autocrine endothelial Notch signaling, and suggests that Dll4 may be a suitable target for intervention in arterial angiogenesis.
人类、小鼠和斑马鱼中功能获得性和功能丧失性突变均已证明Notch信号通路参与血管发育。在斑马鱼中,Notch信号通过抑制发育中的动脉细胞的静脉命运来决定动脉特性。在小鼠中,Notch4受体和Delta样4(Dll4)配体在动脉内皮细胞中特异性表达,提示有类似作用。我们在此表明,单独的Dll4配体在发育过程中对正常动脉模式形成具有剂量敏感性需求。这表明Dll4是自分泌内皮Notch信号的特异性哺乳动物内皮配体,并提示Dll4可能是动脉血管生成干预的合适靶点。