Abstract
Vascular endothelial growth factor (VEGF) mRNA expression was analysed in rabbit vascular smooth muscle cells following exposure to hypoxia and platelet-derived growth factor-BB (PDGF-BB). Hypoxia potently upregulated VEGF mRNA steady-state levels in a time- and concentration-dependent manner reaching a maximum level (approximately 30-fold increase) after 12-24 h at 0% 0(2). In contrast, PDGF-BB caused a modest increase in VEGF expression. However, the combination of PDGF-BB and a threshold hypoxic stimulus (2.5% O2 for 4 h) had a marked synergistic effect. Synergy between hypoxia and PDGF-BB was selective for VEGF expression as hypoxia had no effect on the PDGF-induced upregulation of the proto-oncogene c-myc. These results raise the possibility that hypoxia and PDGF-BB may act in concert to induce VEGF expression in the arterial wall during the development of atherosclerosis.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Base Sequence
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Becaplermin
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Cell Hypoxia*
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Cells, Cultured
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DNA, Complementary
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Endothelial Growth Factors / biosynthesis
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Endothelial Growth Factors / genetics*
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Gene Expression Regulation
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Humans
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Lymphokines / biosynthesis
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Lymphokines / genetics*
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Molecular Sequence Data
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Muscle, Smooth, Vascular / cytology
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Muscle, Smooth, Vascular / metabolism*
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Platelet-Derived Growth Factor / physiology*
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Proto-Oncogene Mas
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Proto-Oncogene Proteins c-sis
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RNA, Messenger / genetics
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RNA, Messenger / metabolism
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Recombinant Proteins
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Up-Regulation
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Vascular Endothelial Growth Factor A
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Vascular Endothelial Growth Factors
Substances
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DNA, Complementary
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Endothelial Growth Factors
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Lymphokines
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MAS1 protein, human
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Platelet-Derived Growth Factor
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Proto-Oncogene Mas
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Proto-Oncogene Proteins c-sis
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RNA, Messenger
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Recombinant Proteins
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Vascular Endothelial Growth Factor A
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Vascular Endothelial Growth Factors
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Becaplermin