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 |
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container_end_page | 1997 |
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container_issue | 11 |
container_start_page | 1989 |
container_title | Biomaterials |
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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 |
format | Article |
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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. 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.</description><identifier>ISSN: 0142-9612</identifier><identifier>EISSN: 1878-5905</identifier><identifier>DOI: 10.1016/j.biomaterials.2006.12.022</identifier><identifier>PMID: 17239947</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>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</subject><ispartof>Biomaterials, 2007-04, Vol.28 (11), p.1989-1997</ispartof><rights>Elsevier Ltd</rights><rights>2007 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c592t-fd67fa7de81f86bf13a52944a7e53b05335803a512dc6611f374bdb5f34e2f643</citedby><cites>FETCH-LOGICAL-c592t-fd67fa7de81f86bf13a52944a7e53b05335803a512dc6611f374bdb5f34e2f643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.biomaterials.2006.12.022$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3538,27906,27907,45977</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17239947$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kitajima, Takashi</creatorcontrib><creatorcontrib>Terai, Hiroshi</creatorcontrib><creatorcontrib>Ito, Yoshihiro</creatorcontrib><title>A fusion protein of hepatocyte growth factor for immobilization to collagen</title><title>Biomaterials</title><addtitle>Biomaterials</addtitle><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.</description><subject>Advanced Basic Science</subject><subject>Angiogenesis</subject><subject>Animals</subject><subject>Baculovirus</subject><subject>Biocompatible Materials - chemistry</subject><subject>Cells, Cultured</subject><subject>Collagen</subject><subject>Collagen - chemistry</subject><subject>Dentistry</subject><subject>Dose-Response Relationship, Drug</subject><subject>Endothelial cells</subject><subject>Endothelial Cells - cytology</subject><subject>Endothelial Cells - metabolism</subject><subject>Fibronectins - chemistry</subject><subject>Growth factors</subject><subject>Hepatocyte Growth Factor - metabolism</subject><subject>HGF</subject><subject>Humans</subject><subject>Immobilization</subject><subject>Neovascularization, Pathologic</subject><subject>Protein Structure, Tertiary</subject><subject>Recombinant Fusion Proteins - chemistry</subject><subject>Regeneration</subject><subject>Time Factors</subject><subject>Tissue Engineering - methods</subject><issn>0142-9612</issn><issn>1878-5905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUk1v1DAUtBAVXQp_AUUcuCX4I7ZjDkhV-VQrcQDOluM8t16SeLGdou2vx9GuBOqltWRZz5qZN3rzEHpNcEMwEW-3Te_DZDJEb8bUUIxFQ2iDKX2CNqSTXc0V5k_RBpOW1koQeoqep7TFpcYtfYZOiaRMqVZu0OV55Zbkw1ztYsjg5yq46gZ2Jge7z1Bdx_An31TO2Bxi5cr10xR6P_o7k1daDpUN42iuYX6BTlwxBC-P7xn6-enjj4sv9dW3z18vzq9qyxXNtRuEdEYO0BHXid4RZjhVbWskcNZjzhjvcPkjdLBCEOKYbPuh5461QJ1o2Rl6c9Atln8vkLKefLJQTMwQlqRFp6SQTD0IpIrKMp3uQSBRQhHFxWOAlHdsVXx3ANoYUorg9C76ycS9JlivKeqt_j9FvaaoCdUlxUJ-deyy9BMM_6jH2ArgwwEAZcy3HqJO1sNsYfARbNZD8I_r8_6ejB397K0Zf8Ee0jYscV45RKdC0N_XfVrXCUtcjuTsL1AFyXk</recordid><startdate>20070401</startdate><enddate>20070401</enddate><creator>Kitajima, Takashi</creator><creator>Terai, Hiroshi</creator><creator>Ito, Yoshihiro</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>F28</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20070401</creationdate><title>A fusion protein of hepatocyte growth factor for immobilization to collagen</title><author>Kitajima, Takashi ; 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 & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kitajima, Takashi</au><au>Terai, Hiroshi</au><au>Ito, Yoshihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A fusion protein of hepatocyte growth factor for immobilization to collagen</atitle><jtitle>Biomaterials</jtitle><addtitle>Biomaterials</addtitle><date>2007-04-01</date><risdate>2007</risdate><volume>28</volume><issue>11</issue><spage>1989</spage><epage>1997</epage><pages>1989-1997</pages><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>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.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>17239947</pmid><doi>10.1016/j.biomaterials.2006.12.022</doi><tpages>9</tpages></addata></record> |
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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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