Plasmin activates the lymphangiogenic growth factors VEGF-C and VEGF-D
- McColl, BK; Baldwin, ME; Roufail, S; Freeman, C; Moritz, RL; Simpson, RJ; Alitalo, K; Stacker, SA; Achen, MG;
Publication Year 2003-09-15, Volume 198, Issue #6, Page 863-868
- Journal Title
- JOURNAL OF EXPERIMENTAL MEDICINE
- Publication Type
- Journal Article
- Vascular endothelial growth factor (VEGF) C and VEGF-D stimulate lymphangiogenesis and angiogenesis in tissues and tumors by activating the endothelial cell surface receptor tyrosine kinases VEGF receptor (VEGFR) 2 and VEGFR-3. These growth factors are secreted as full-length inactive forms consisting of NH2- and COOH-terminal propeptides and a central VEGF homology domain (VHD) containing receptor binding sites. Proteolytic cleavage removes the propeptides to generate mature forms, consisting of dimers of the VEGF homology domain, that bind receptors with much greater affinity than the full-length forms. Therefore, proteolytic processing activates VEGF-C and VEGF-D, although the proteases involved were unknown. Here, we report that the serine protease plasmin cleaved both propeptides from the VEGF homology domain of human VEGF-D and thereby generated a mature form exhibiting greatly enhanced binding and cross-linking of VEGFR-2 and VEGFR-3 in comparison to full-length material. Plasmin also activated VEGF-C. As lymphangiogenic growth factors promote the metastatic spread of cancer via the lymphatics, the proteolytic activation of these molecules represents a potential target for antimetastatic agents. Identification of an enzyme that activates the lymphangiogenic growth factors will facilitate development of inhibitors of metastasis.
- ROCKEFELLER UNIV PRESS
- TERM-FOLLOW-UP; FACTOR RECEPTOR-3; TUMOR LYMPHANGIOGENESIS; TYROSINE KINASES; BREAST-CARCINOMA; TRANSGENIC MICE; D EXPRESSION; METASTASIS; PROMOTES; CELLS
- Publisher's Version
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Creation Date: 2003-09-15 12:00:00Last Modified: 0001-01-01 12:00:00