A fusion protein of hepatocyte growth factor for immobilization to collagen

Abstract We describe here a fusion protein consisting of hepatocyte growth factor (HGF; an angiogenic factor) and a collagen-binding domain (CBD) polypeptide of fibronectin (FN). This fusion protein (CBD-HGF), produced by a baculovirus expression system, exhibited much stronger collagen binding acti...

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Veröffentlicht in:Biomaterials 2007-04, Vol.28 (11), p.1989-1997
Hauptverfasser: Kitajima, Takashi, Terai, Hiroshi, Ito, Yoshihiro
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container_end_page 1997
container_issue 11
container_start_page 1989
container_title Biomaterials
container_volume 28
creator Kitajima, Takashi
Terai, Hiroshi
Ito, Yoshihiro
description Abstract We describe here a fusion protein consisting of hepatocyte growth factor (HGF; an angiogenic factor) and a collagen-binding domain (CBD) polypeptide of fibronectin (FN). This fusion protein (CBD-HGF), produced by a baculovirus expression system, exhibited much stronger collagen binding activity than native HGF in the range of 0.4–6.4 μg/ml. Its binding at the lowest concentration exceeded that of HGF at the highest concentration. In addition, the collagen-bound CBD-HGF promoted growth of endothelial cells (ECs) to a greater degree at least 4 days longer than HGF added to the culture medium; about 5-fold greater increase in cell number after 10 days. These findings suggest that the fused CBD moiety not only helped immobilize HGF on collagen but also helped stabilize the fusion molecule, resulting in prolonged activity. The angiogenic activity of CBD-HGF in animal tissues was examined by subcutaneously implanting collagen sponges containing bound CBD-HGF. Blood vessel formation in the sponges after 7 days was 4–6-fold extensive as compared to the control sponges without sample. Implanted sponges with native HGF did not show significant difference from control. These results indicate that CBD-HGF is suitable for in vitro culture of ECs, and that this fusion protein can be used to confer HGF activity on biomaterials for use in tissue engineering.
doi_str_mv 10.1016/j.biomaterials.2006.12.022
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This fusion protein (CBD-HGF), produced by a baculovirus expression system, exhibited much stronger collagen binding activity than native HGF in the range of 0.4–6.4 μg/ml. Its binding at the lowest concentration exceeded that of HGF at the highest concentration. In addition, the collagen-bound CBD-HGF promoted growth of endothelial cells (ECs) to a greater degree at least 4 days longer than HGF added to the culture medium; about 5-fold greater increase in cell number after 10 days. These findings suggest that the fused CBD moiety not only helped immobilize HGF on collagen but also helped stabilize the fusion molecule, resulting in prolonged activity. The angiogenic activity of CBD-HGF in animal tissues was examined by subcutaneously implanting collagen sponges containing bound CBD-HGF. Blood vessel formation in the sponges after 7 days was 4–6-fold extensive as compared to the control sponges without sample. Implanted sponges with native HGF did not show significant difference from control. 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Terai, Hiroshi ; Ito, Yoshihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c592t-fd67fa7de81f86bf13a52944a7e53b05335803a512dc6611f374bdb5f34e2f643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Advanced Basic Science</topic><topic>Angiogenesis</topic><topic>Animals</topic><topic>Baculovirus</topic><topic>Biocompatible Materials - chemistry</topic><topic>Cells, Cultured</topic><topic>Collagen</topic><topic>Collagen - chemistry</topic><topic>Dentistry</topic><topic>Dose-Response Relationship, Drug</topic><topic>Endothelial cells</topic><topic>Endothelial Cells - cytology</topic><topic>Endothelial Cells - metabolism</topic><topic>Fibronectins - chemistry</topic><topic>Growth factors</topic><topic>Hepatocyte Growth Factor - metabolism</topic><topic>HGF</topic><topic>Humans</topic><topic>Immobilization</topic><topic>Neovascularization, Pathologic</topic><topic>Protein Structure, Tertiary</topic><topic>Recombinant Fusion Proteins - chemistry</topic><topic>Regeneration</topic><topic>Time Factors</topic><topic>Tissue Engineering - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kitajima, Takashi</creatorcontrib><creatorcontrib>Terai, Hiroshi</creatorcontrib><creatorcontrib>Ito, Yoshihiro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical &amp; 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source MEDLINE; Elsevier ScienceDirect Journals
subjects Advanced Basic Science
Angiogenesis
Animals
Baculovirus
Biocompatible Materials - chemistry
Cells, Cultured
Collagen
Collagen - chemistry
Dentistry
Dose-Response Relationship, Drug
Endothelial cells
Endothelial Cells - cytology
Endothelial Cells - metabolism
Fibronectins - chemistry
Growth factors
Hepatocyte Growth Factor - metabolism
HGF
Humans
Immobilization
Neovascularization, Pathologic
Protein Structure, Tertiary
Recombinant Fusion Proteins - chemistry
Regeneration
Time Factors
Tissue Engineering - methods
title A fusion protein of hepatocyte growth factor for immobilization to collagen
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