Cell-Demanded Liberation of VEGF121 From Fibrin Implants Induces Local and Controlled Blood Vessel Growth

• Published in: Circulation research 2004-04, Vol.94 (8), p.1124-1132
• Main Authors: Ehrbar, Martin, Djonov, Valentin G, Schnell, Christian, Tschanz, Stefan A, Martiny-Baron, Georg, Schenk, Ursula, Wood, Jeanette, Burri, Peter H, Hubbell, Jeffrey A, Zisch, Andreas H
• Format: Article
• Language: English
• Subjects: Allantois - blood supply; Allantois - drug effects; alpha-2-Antiplasmin - chemistry; alpha-2-Antiplasmin - genetics; Amino Acid Sequence; Animals; Binding Sites; Biological and medical sciences; Capillary Permeability - drug effects; Chick Embryo; Chorion - blood supply; Chorion - drug effects; Diffusion; Drug Implants; Endothelial Cells - drug effects; Endothelial Cells - ultrastructure; Endothelium, Vascular - cytology; Extracellular Matrix Proteins - analysis; Fibrin - administration & dosage; Fibrin - metabolism; Fundamental and applied biological sciences. Psychology; Gels; Humans; Mice; Morphogenesis - drug effects; Myosin Heavy Chains; Neovascularization, Physiologic - drug effects; Nonmuscle Myosin Type IIB; Peptide Fragments - chemistry; Peptide Fragments - genetics; Peptide Fragments - metabolism; Protein Engineering; Protein Structure, Tertiary; Receptor, TIE-2 - analysis; Recombinant Fusion Proteins - chemistry; Recombinant Fusion Proteins - metabolism; Vascular Endothelial Growth Factor A - chemistry; Vascular Endothelial Growth Factor A - genetics; Vascular Endothelial Growth Factor A - metabolism; Vascular Endothelial Growth Factor Receptor-2 - analysis; Vertebrates: cardiovascular system
• ISSN: 0009-7330; 1524-4571
• DOI: 10.1161/01.RES.0000126411.29641.08

ABSTRACT—Although vascular endothelial growth factor (VEGF) has been described as a potent angiogenic stimulus, its application in therapy remains difficultblood vessels formed by exposure to VEGF tend to be malformed and leaky. In nature, the principal form of VEGF possesses a binding site for ECM components that maintain it in the immobilized state until released by local cellular enzymatic activity. In this study, we present an engineered variant form of VEGF, α2PI1–8- VEGF121, that mimics this concept of matrix-binding and cell-mediated release by local cell–associated enzymatic activity, working in the surgically-relevant biological matrix fibrin. We show that matrix-conjugated α2 PI1–8- VEGF121 is protected from clearance, contrary to native VEGF121 mixed into fibrin, which was completely released as a passive diffusive burst. Grafting studies on the embryonic chicken chorioallantoic membrane (CAM) and in adult mice were performed to assess and compare the quantity and quality of neovasculature induced in response to fibrin implants formulated with matrix-bound α2 PI1–8- VEGF121 or native diffusible VEGF121. Our CAM measurements demonstrated that cell-demanded release of α2 PI1–8- VEGF121 increases the formation of new arterial and venous branches, whereas exposure to passively released wild-type VEGF121 primarily induced chaotic changes within the capillary plexus. Specifically, our analyses at several levels, from endothelial cell morphology and endothelial interactions with periendothelial cells, to vessel branching and network organization, revealed that α2 PI1–8- VEGF121 induces vessel formation more potently than native VEGF121 and that those vessels possess more normal morphologies at the light microscopic and ultrastructural level. Permeability studies in mice validated that vessels induced by α2 PI1–8- VEGF121 do not leak. In conclusion, cell-demanded release of engineered VEGF121 from fibrin implants may present a therapeutically safe and practical modality to induce local angiogenesis.