scholarly journals Notch ligand Delta-like 1 promotes the metastasis of melanoma by enhancing tumor adhesion

2014 ◽  
Vol 47 (4) ◽  
pp. 299-306 ◽  
Author(s):  
J.P. Zhang ◽  
N. Li ◽  
W.Z. Bai ◽  
X.C. Qiu ◽  
B.A. Ma ◽  
...  
Keyword(s):  
Genetics ◽  
2016 ◽  
Vol 202 (3) ◽  
pp. 1119-1133 ◽  
Author(s):  
K. Schuster-Gossler ◽  
R. Cordes ◽  
J. Muller ◽  
I. Geffers ◽  
P. Delany-Heiken ◽  
...  

Cytotherapy ◽  
2015 ◽  
Vol 17 (5) ◽  
pp. 579-592 ◽  
Author(s):  
Hyojin Kim ◽  
Lan Huang ◽  
Paul J. Critser ◽  
Zhenyun Yang ◽  
Rebecca J. Chan ◽  
...  

2005 ◽  
Vol 26 (7) ◽  
pp. 881-886 ◽  
Author(s):  
Yan PAN ◽  
Qian-liu SONG ◽  
Yan-hua LIN ◽  
Ning LU ◽  
He-ming YU ◽  
...  

2000 ◽  
Vol 113 (23) ◽  
pp. 4313-4318 ◽  
Author(s):  
B. Varnum-Finney ◽  
L. Wu ◽  
M. Yu ◽  
C. Brashem-Stein ◽  
S. Staats ◽  
...  

Cell-cell interactions mediated by Notch and its ligands are known to effect many cell fate decisions in both invertebrates and vertebrates. However, the mechanisms involved in ligand induced Notch activation are unknown. Recently it was shown that, in at least some cases, endocytosis of the extracellular domain of Notch and ligand by the signaling cell is required for signal induction in the receptive cell. These results imply that soluble ligands (ligand extracellular domains) although capable of binding Notch would be unlikely to activate it. To test the potential activity of soluble Notch ligands, we generated monomeric and dimeric forms of the Notch ligand Delta-1 by fusing the extracellular domain to either a series of myc epitopes (Delta-1(ext-myc)) or to the Fc portion of human IgG-1 (Delta-1(ext-IgG)), respectively. Notch activation, assayed by inhibition of differentiation in C2 myoblasts and by HES1 transactivation in U20S cells, occurred when either Delta-1(ext-myc) or Delta-1(ext-IgG) were first immobilized on the plastic surface. However, Notch was not activated by either monomeric or dimeric ligand in solution (non-immobilized). Furthermore, both non-immobilized Delta-1(ext-myc) and Delta-1(ext-IgG) blocked the effect of immobilized Delta. These results indicate that Delta-1 extracellular domain must be immobilized to induce Notch activation in C2 or U20S cells and that non-immobilized Delta-1 extracellular domain is inhibitory to Notch function. These results imply that ligand stabilization may be essential for Notch activation.


Development ◽  
1998 ◽  
Vol 125 (15) ◽  
pp. 2951-2962 ◽  
Author(s):  
T. Klein ◽  
A.M. Arias

The Notch signalling pathway plays an important role during the development of the wing primordium, especially of the wing blade and margin. In these processes, the activity of Notch is controlled by the activity of the dorsal specific nuclear protein Apterous, which regulates the expression of the Notch ligand, Serrate, and the Fringe signalling molecule. The other Notch ligand, Delta, also plays a role in the development and patterning of the wing. It has been proposed that Fringe modulates the ability of Serrate and Delta to signal through Notch and thereby restricts Notch signalling to the dorsoventral boundary of the developing wing blade. Here we report the results of experiments aimed at establishing the relationships between Fringe, Serrate and Delta during wing development. We find that Serrate is not required for the initiation of wing development but rather for the expansion and early patterning of the wing primordium. We provide evidence that, at the onset of wing development, Delta is under the control of apterous and might be the Notch ligand in this process. In addition, we find that Fringe function requires Su(H). Our results suggest that Notch signalling during wing development relies on careful balances between positive and dominant negative interactions between Notch ligands, some of which are mediated by Fringe.


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