Ligand-Dependent Notch Signaling in Vascular Formation

Notch信号通路 血管生成 细胞生物学 萌芽血管生成 生物 Notch蛋白质类 Hes3信号轴 信号转导 内皮干细胞 内皮 细胞命运测定 转录因子 神经科学 新生血管 遗传学 基因 体外
作者
Tsutomu Kume
出处
期刊:Advances in Experimental Medicine and Biology [Springer Nature]
卷期号:727: 210-222 被引量:82
标识
DOI:10.1007/978-1-4614-0899-4_16
摘要

The Notch signaling pathway is a critical component of vascular formation and morphogenesis in both development and disease. Compelling evidence indicates that Notch signaling is required for the induction of arterial-cell fate during development and for the selection of endothelial tip and stalk cells during sprouting angiogenesis. In mammals, two of the four Notch receptors (Notch1 and Notch4) and three of the five Notch ligands (Jagged1, Dll1 and Dll4) are predominantly expressed in vascular endothelial cells and are important for many aspects of vascular biology. During arterial cell-fate selection and angiogenesis, the roles of Notch1 and Notch4 are thought to be similar and the role of Dll4 is well-characterized. However, the molecular mechanisms that determine the functional similarities and differences of Notch ligands in vascular endothelial cells remain largely unknown; consequently, additional research is needed to elucidate the ligand-specific functions and mechanisms associated with Notch activation in the vascular endothelium. Results from recent studies indicate that Dll1 and Dll4 have distinct roles in the specification and maintenance of arterial cell identity, while Dll4 and Jagged1 have opposing effects on tip- and stalk-cell selection during sprouting angiogenesis. This chapter will focus on the newly discovered, distinct roles of several Notch ligands in the regulation of blood vessel formation and will provide perspectives for future research in the field.
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