Leslie Jonathan D, Ariza-McNaughton Linda, Bermange Adam L, McAdow Ryan, Johnson Stephen L, Lewis Julian
Vertebrate Development Laboratory, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.
Development. 2007 Mar;134(5):839-44. doi: 10.1242/dev.003244. Epub 2007 Jan 24.
Notch signalling by the ligand Delta-like 4 (Dll4) is essential for normal vascular remodelling, yet the precise way in which the pathway influences the behaviour of endothelial cells remains a mystery. Using the embryonic zebrafish, we show that, when Dll4-Notch signalling is defective, endothelial cells continue to migrate and proliferate when they should normally stop these processes. Artificial overactivation of the Notch pathway has opposite consequences. When vascular endothelial growth factor (Vegf) signalling and Dll4-Notch signalling are both blocked, the endothelial cells remain quiescent. Thus, Dll4-Notch signalling acts as an angiogenic ;off' switch by making endothelial cells unresponsive to Vegf.
由配体Delta样4(Dll4)介导的Notch信号对于正常血管重塑至关重要,然而该信号通路影响内皮细胞行为的确切方式仍是个谜。利用斑马鱼胚胎,我们发现,当Dll4-Notch信号有缺陷时,内皮细胞在正常情况下应停止这些过程时仍继续迁移和增殖。Notch信号通路的人工过度激活则会产生相反的结果。当血管内皮生长因子(Vegf)信号和Dll4-Notch信号均被阻断时,内皮细胞保持静止。因此,Dll4-Notch信号通过使内皮细胞对Vegf无反应而充当血管生成的“关闭”开关。