Article (Scientific journals)
New prospects in the roles of the C-terminal domains of VEGF-A and their cooperation for ligand binding, cellular signaling and vessels formation.
Delcombel, Romain; Janssen, Lauriane; Vassy, Roger et al.
2013In Angiogenesis, 16 (2), p. 353-71
Peer Reviewed verified by ORBi
 

Files


Full Text
Delcombel R Angio 2013.pdf
Publisher postprint (2.25 MB)
Request a copy

All documents in ORBi are protected by a user license.

Send to



Details



Keywords :
VEGF isoforms; Angiogenesis; Neuropilin-1; VEGF receptor; Alternative splicing
Abstract :
[en] VEGF-A is a crucial growth factor for blood vessel homeostasis and pathological angiogenesis. Due to alternative splicing of its pre-mRNA, VEGF-A is produced under several isoforms characterized by the combination of their C-terminal domains, which determines their respective structure, availability and affinity for co-receptors. As controversies still exist about the specific roles of these exon-encoded domains, we systematically compared the properties of eight natural and artificial variants containing the domains encoded by exons 1-4 and various combinations of the domains encoded by exons 5, 7 and 8a or 8b. All the variants (VEGF(111)a, VEGF(111)b, VEGF(121)a, VEGF(121)b, VEGF(155)a, VEGF(155)b, VEGF(165)a, VEGF(165)b) have a similar affinity for VEGF-R2, as determined by Surface plasmon resonance analyses. They strongly differ however in terms of binding to neuropilin-1 and heparin/heparan sulfate proteoglycans. Data indicate that the 6 amino acids encoded by exon 8a must be present and cooperate with those of exons 5 or 7 for efficient binding, which was confirmed in cell culture models. We further showed that VEGF(165)b has inhibitory effects in vitro, as previously reported, but that the shortest VEGF variant possessing also the 6 amino acids encoded by exon 8b (VEGF(111)b) is remarkably proangiogenic, demonstrating the critical importance of domain interactions for defining the VEGF properties. The number, size and localization of newly formed blood vessels in a model of tumour angiogenesis strongly depend also on the C-terminal domain composition, suggesting that association of several VEGF isoforms may be more efficient for treating ischemic diseases than the use of any single variant.
Disciplines :
Biochemistry, biophysics & molecular biology
Author, co-author :
Delcombel, Romain ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Laboratoire des tissus conjonctifs
Janssen, Lauriane ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Laboratoire des tissus conjonctifs
Vassy, Roger
Gammons, Melissa
Haddad, Oualid
Richard, Benjamin
Letourneur, Didier
Bates, David
Hendricks, Céline
Waltenberger, Johannes
Starzec, Anna
Sounni, Nor Eddine  ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biologie cellulaire et moléculaire appliquée à l'homme
Noël, Agnès ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biologie cellulaire et moléculaire appliquée à l'homme
Deroanne, Christophe ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Laboratoire des tissus conjonctifs
Lambert, Charles ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Laboratoire des tissus conjonctifs
Colige, Alain ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Laboratoire des tissus conjonctifs
More authors (6 more) Less
Language :
English
Title :
New prospects in the roles of the C-terminal domains of VEGF-A and their cooperation for ligand binding, cellular signaling and vessels formation.
Publication date :
2013
Journal title :
Angiogenesis
ISSN :
0969-6970
eISSN :
1573-7209
Publisher :
Kluwer Academic Publishers, Dordrecht, Netherlands
Volume :
16
Issue :
2
Pages :
353-71
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 22 January 2013

Statistics


Number of views
89 (24 by ULiège)
Number of downloads
2 (2 by ULiège)

Scopus citations®
 
48
Scopus citations®
without self-citations
42
OpenCitations
 
45

Bibliography


Similar publications



Contact ORBi