Synthesis and physiological activity of heterodimers comprising different splice forms of vascular endothelial growth factor and placenta growth factor

被引:45
作者
Birkenhager, R
Schneppe, B
Rockl, W
Wilting, J
Weich, HA
McCarthy, JEG
机构
[1] NATL BIOTECHNOL RES CTR,DEPT GENE EXPRESS,D-38124 BRAUNSCHWEIG,GERMANY
[2] UNIV FREIBURG,INST ANAT 2,D-79104 FREIBURG,GERMANY
关键词
D O I
10.1042/bj3160703
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
Vascular endothilial growth factor (VEGF) and placenta growth factor (PIGF) are members of a dimeric-growth-factor family with angiogenic properties. VEGF is a highly potent and specific mitogen for endothelial cells, playing a vital role in angiogenesis in vivo. The role of PIGF is less clear. We expressed the monomeric splice forms VEGF-165, VEGF-121, PIGF-1 and PIGF-2 as unfused genes in Escherichia coli using the pCYTEXP expression system. In vitro dimerization experiments revealed that both homo- and hetero-dimers can be formed from these monomeric proteins. The dimers were tested for their ability to promote capillary growth in vivo and stimulate DNA synthesis in cultured human vascular endothelial cells. Heterodimers comprising different VEGF splice forms, or combinations of VEGF/PIGF splice forms, showed mitogenic activity. The results demonstrate that four different heterodimeric growth factors are likely to have as yet uncharacterized functions in vivo.
引用
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页码:703 / 707
页数:5
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