The Notch Ligands Dll4 and Jagged1 Have Opposing Effects on Angiogenesis

被引:893
作者
Benedito, Rui [1 ,2 ,3 ]
Roca, Cristina [1 ]
Soerensen, Inga [4 ]
Adams, Susanne [1 ,2 ,3 ]
Gossler, Achim [4 ]
Fruttiger, Marcus [5 ]
Adams, Ralf H. [1 ,2 ,3 ]
机构
[1] Canc Res UK London Res Inst, Vasc Dev Lab, London WC2A 3PX, England
[2] Max Planck Inst Mol Biomed, Dept Tissue Morphogenesis, D-48149 Munster, Germany
[3] Univ Munster, Fac Med, D-48149 Munster, Germany
[4] Hannover Med Sch, Inst Mol Biol OE5250, D-30625 Hannover, Germany
[5] UCL, Inst Ophthalmol, London EC1V 9EL, England
关键词
INHIBITS TUMOR-GROWTH; ENDOTHELIAL-CELLS; CRE-RECOMBINASE; EXPRESSION; DEFECTS; PATHWAY; DELTA1; PROTEOLYSIS; ACTIVATION; REGULATOR;
D O I
10.1016/j.cell.2009.03.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Notch pathway is a highly conserved signaling system that controls a diversity of growth, differentiation, and patterning processes. In growing blood vessels, sprouting of endothelial tip cells is inhibited by Notch signaling, which is activated by binding of the Notch receptor to its ligand Delta-like 4 (Dll4). Here, we show that the Notch ligand Jagged1 is a potent proangiogenic regulator in mice that antagonizes Dll4-Notch signaling in cells expressing Fringe family glycosyltransferases. Upon glycosylation of Notch, Dll4-Notch signaling is enhanced, whereas Jagged1 has weak signaling capacity and competes with Dll4. Our findings establish that the equilibrium between two Notch ligands with distinct spatial expression patterns and opposing functional roles regulates angiogenesis, a mechanism that might also apply to other Notch-controlled biological processes.
引用
收藏
页码:1124 / 1135
页数:12
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