Matrix Metalloproteinases Cleave Connective Tissue Growth Factor and Reactivate Angiogenic Activity of Vascular Endothelial Growth Factor 165

• Published in: The Journal of biological chemistry Vol. 277; no. 39; pp. 36288 - 36295
• Main Authors: Hashimoto, Gakuji, Inoki, Isao, Fujii, Yutaka, Aoki, Takanori, Ikeda, Eiji, Okada, Yasunori
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 27.09.2002; American Society for Biochemistry and Molecular Biology
• Subjects: Animals; Aorta - cytology; Binding Sites; Cattle; Collagenases - metabolism; Connective Tissue Growth Factor; DNA, Complementary - metabolism; Endothelial Growth Factors - metabolism; Endothelium, Vascular - cytology; Fibrinolysin - metabolism; Humans; Immediate-Early Proteins - metabolism; Immunoblotting; Intercellular Signaling Peptides and Proteins - metabolism; Lymphokines - metabolism; Matrix Metalloproteinase 1 - metabolism; Matrix Metalloproteinase 13; Matrix Metalloproteinase 3 - metabolism; Matrix Metalloproteinase 7 - metabolism; Matrix Metalloproteinases - metabolism; Neovascularization, Pathologic; Neovascularization, Physiologic; Pancreatic Elastase - metabolism; Protein Binding; Recombinant Proteins - metabolism; Serine Endopeptidases - metabolism; Time Factors; Vascular Endothelial Growth Factor A; Vascular Endothelial Growth Factors
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M201674200

Vascular endothelial growth factor (VEGF), a potent angiogenic mitogen, plays a crucial role in angiogenesis under various pathophysiological conditions. We have recently demonstrated that VEGF165, one of the VEGF isoforms, binds connective tissue growth factor (CTGF) and that its angiogenic activity is inhibited in the VEGF165·CTGF complex form (Inoki, I., Shiomi, T., Hashimoto, G., Enomoto, H., Nakamura, H., Makino, K., Ikeda, E., Takata, S., Kobayashi, K. and Okada, Y. (2002) FASEB J. 16, 219–221). In the present study, we further examined the susceptibility of the VEGF165·CTGF complex to matrix metalloproteinases (MMP-1, -2, -3, -7, -9, and -13), ADAMTS4 (aggrecanase-1), and serine proteinases, and evaluated the recovery of the angiogenic activity of VEGF165 after the treatment. Among the MMPs, MMP-1, -3, -7, and -13 processed CTGF of the complex into the major NH2- and COOH-terminal fragments, whereas VEGF165 was completely resistant to the MMPs. On the other hand, elastase and plasmin cleaved both CTGF and VEGF165 of the complex, but they were completely resistant to ADAMTS4. By digestion of the immobilized VEGF165·CTGF complex with MMP-3 or MMP-7, both NH2- and COOH-terminal fragments of CTGF were dissociated and released from the complex into the liquid phase. The in vitro angiogenic activity of VEGF165 blocked in the VEGF165·CTGF complex was reactivated to original levels after CTGF digestion of the complex with MMP-1, -3, and -13. Recovery of angiogenic activity was further confirmed by in vivoangiogenesis assay using a Matrigel injection model in mice. These results demonstrate for the first time that CTGF is a substrate of MMPs and that the angiogenic activity of VEGF165 suppressed by the complex formation with CTGF is recovered through the selective degradation of CTGF by MMPs. MMPs may play a novel role through CTGF degradation in VEGF-induced angiogenesis during embryonic development, tissue maintenance, and/or pathological processes of various diseases.