Angiogenic synergy of bFGF and VEGF is antagonized by Angiopoietin-2 in a modified in vivo Matrigel assay

被引:56
作者
Ley, CD [1 ]
Olsen, MWB [1 ]
Lund, EL [1 ]
Kristjansen, PEG [1 ]
机构
[1] Univ Copenhagen, Inst Mol Pathol, Expt Oncol Lab, DK-2100 Copenhagen, Denmark
关键词
bFGF; VEGF; Ang-2; angiogenesis; matrigel; synergy; migration;
D O I
10.1016/j.mvr.2004.06.002
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
A murine modification of the Matrigel chamber assay originally developed for use on rats is presented. This modified assay permits improved quantification due to subcutaneous Matrigel implants of constant shape and volume. We have quantitatively assessed the angiogenic potential of the growth factors basic fibroblast growth factor (bFGF), VEGF, and Angiopoietin-2 (Ang-2) with special emphasis on their mutual interactions. A reproducible dose-response relationship for bFGF was established for doses between 150 and 1000 ng per chamber, whereas VEGF did not display angiogenic activity on its own in the tested dose of up to 200 ng per chamber. Conversely, we found a strong synergistic action of bFGF and VEGF when combined in a 3:1 ratio. Two other combinations (ratios) with greater VEGF doses were also tested, but the synergistic effect was only observed when 50 ng of VEGF was added to 150 ng per chamber of bFGF. This synergistic effect of bFGF and VEGF was significantly reduced by further addition of 100 ng Angiopoietin-2. Inhibition of the response to bFGF and VEGF was confirmed by in vitro EC migration experiments, which, together with our in vivo results, indicates that Ang-2 may target chemotactic responses to bFGF and VEGF in vivo. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:161 / 168
页数:8
相关论文
共 35 条
[1]   The sponge/Matrigel angiogenesis assay [J].
Akhtar N. ;
Dickerson E.B. ;
Auerbach R. .
Angiogenesis, 2002, 5 (1-2) :75-80
[2]   Tie2 receptor ligands, angiopoietin-1 and angiopoietin-2, modulate VEGF-induced postnatal neovascularization [J].
Asahara, T ;
Chen, DH ;
Takahashi, T ;
Fujikawa, K ;
Kearney, M ;
Magner, M ;
Yancopoulos, GD ;
Isner, JM .
CIRCULATION RESEARCH, 1998, 83 (03) :233-240
[3]  
COCKERILL GW, 1995, INT REV CYTOL, V159, P113, DOI 10.1016/S0074-7696(08)62106-3
[4]   TUMOR VASCULAR-PERMEABILITY FACTOR STIMULATES ENDOTHELIAL-CELL GROWTH AND ANGIOGENESIS [J].
CONNOLLY, DT ;
HEUVELMAN, DM ;
NELSON, R ;
OLANDER, JV ;
EPPLEY, BL ;
DELFINO, JJ ;
SIEGEL, NR ;
LEIMGRUBER, RM ;
FEDER, J .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (05) :1470-1478
[5]   VEGF-receptor signal transduction [J].
Cross, MJ ;
Dixelius, J ;
Matsumoto, T ;
Claesson-Welsh, L .
TRENDS IN BIOCHEMICAL SCIENCES, 2003, 28 (09) :488-494
[6]   Isolation of Angiopoietin-1, a ligand for the TIE2 receptor, by secretion-trap expression cloning [J].
Davis, S ;
Aldrich, TH ;
Jones, PF ;
Acheson, A ;
Compton, DL ;
Jain, V ;
Ryan, TE ;
Bruno, J ;
Radziejewski, C ;
Maisonpierre, PC ;
Yancopoulos, GD .
CELL, 1996, 87 (07) :1161-1169
[7]  
Dellian M, 1996, AM J PATHOL, V149, P59
[8]  
DVORAK HF, 1984, CANCER RES, V44, P3348
[9]  
DVORAK HF, 1979, JNCI-J NATL CANCER I, V62, P1459
[10]   Vascular permeability factor/vascular endothelial growth factor: A critical cytokine in tumor angiogenesis and a potential target for diagnosis and therapy [J].
Dvorak, HF .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (21) :4368-4380