Engineering the mechanical and biological properties of nanofibrous vascular grafts for in situ vascular tissue engineering
Synthetic small diameter vascular grafts have a high failure rate, and endothelialization is critical for preventing thrombosis and graft occlusion. A promising approach is in situ tissue engineering, whereby an acellular scaffold is implanted and provides stimulatory cues to guide the in situ remod...
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Veröffentlicht in: | Biofabrication 2017-08, Vol.9 (3), p.035007-035007 |
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creator | Henry, Jeffrey J D Yu, Jian Wang, Aijun Lee, Randall Fang, Jun Li, Song |
description | Synthetic small diameter vascular grafts have a high failure rate, and endothelialization is critical for preventing thrombosis and graft occlusion. A promising approach is in situ tissue engineering, whereby an acellular scaffold is implanted and provides stimulatory cues to guide the in situ remodeling into a functional blood vessel. An ideal scaffold should have sufficient binding sites for biomolecule immobilization and a mechanical property similar to native tissue. Here we developed a novel method to blend low molecular weight (LMW) elastic polymer during electrospinning process to increase conjugation sites and to improve the mechanical property of vascular grafts. LMW elastic polymer improved the elasticity of the scaffolds, and significantly increased the amount of heparin conjugated to the micro/nanofibrous scaffolds, which in turn increased the loading capacity of vascular endothelial growth factor (VEGF) and prolonged the release of VEGF. Vascular grafts were implanted into the carotid artery of rats to evaluate the in vivo performance. VEGF treatment significantly enhanced endothelium formation and the overall patency of vascular grafts. Heparin coating also increased cell infiltration into the electrospun grafts, thus increasing the production of collagen and elastin within the graft wall. This work demonstrates that LMW elastic polymer blending is an approach to engineer the mechanical and biological property of micro/nanofibrous vascular grafts for in situ vascular tissue engineering. |
doi_str_mv | 10.1088/1758-5090/aa834b |
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A promising approach is in situ tissue engineering, whereby an acellular scaffold is implanted and provides stimulatory cues to guide the in situ remodeling into a functional blood vessel. An ideal scaffold should have sufficient binding sites for biomolecule immobilization and a mechanical property similar to native tissue. Here we developed a novel method to blend low molecular weight (LMW) elastic polymer during electrospinning process to increase conjugation sites and to improve the mechanical property of vascular grafts. LMW elastic polymer improved the elasticity of the scaffolds, and significantly increased the amount of heparin conjugated to the micro/nanofibrous scaffolds, which in turn increased the loading capacity of vascular endothelial growth factor (VEGF) and prolonged the release of VEGF. Vascular grafts were implanted into the carotid artery of rats to evaluate the in vivo performance. VEGF treatment significantly enhanced endothelium formation and the overall patency of vascular grafts. Heparin coating also increased cell infiltration into the electrospun grafts, thus increasing the production of collagen and elastin within the graft wall. This work demonstrates that LMW elastic polymer blending is an approach to engineer the mechanical and biological property of micro/nanofibrous vascular grafts for in situ vascular tissue engineering.</description><identifier>ISSN: 1758-5090</identifier><identifier>ISSN: 1758-5082</identifier><identifier>EISSN: 1758-5090</identifier><identifier>DOI: 10.1088/1758-5090/aa834b</identifier><identifier>PMID: 28817384</identifier><identifier>CODEN: BIOFCK</identifier><language>eng</language><publisher>England: IOP Publishing</publisher><subject>Animals ; Antithrombins - pharmacology ; Blood Vessel Prosthesis ; Collagen - metabolism ; Elastin - metabolism ; electrospinning ; endothelialization ; Endothelium - drug effects ; Endothelium - metabolism ; Extracellular Matrix - metabolism ; heparin ; Heparin - pharmacology ; Humans ; Immobilized Proteins - metabolism ; Male ; Mechanical Phenomena ; Myocytes, Smooth Muscle - metabolism ; Nanofibers - chemistry ; polycaprolactone ; Rats ; tissue engineering ; Tissue Engineering - methods ; Tissue Scaffolds - chemistry ; Vascular Endothelial Growth Factor A - metabolism ; vascular endothelial growth factors ; vascular grafts ; Vascular Patency - drug effects</subject><ispartof>Biofabrication, 2017-08, Vol.9 (3), p.035007-035007</ispartof><rights>2017 IOP Publishing Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c500t-36e46c037d7fdcb40e6097a6f9683a4d395d20557125e0a2b39c78e707e309803</citedby><cites>FETCH-LOGICAL-c500t-36e46c037d7fdcb40e6097a6f9683a4d395d20557125e0a2b39c78e707e309803</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://iopscience.iop.org/article/10.1088/1758-5090/aa834b/pdf$$EPDF$$P50$$Giop$$H</linktopdf><link.rule.ids>230,314,780,784,885,27924,27925,53846,53893</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28817384$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Henry, Jeffrey J D</creatorcontrib><creatorcontrib>Yu, Jian</creatorcontrib><creatorcontrib>Wang, Aijun</creatorcontrib><creatorcontrib>Lee, Randall</creatorcontrib><creatorcontrib>Fang, Jun</creatorcontrib><creatorcontrib>Li, Song</creatorcontrib><title>Engineering the mechanical and biological properties of nanofibrous vascular grafts for in situ vascular tissue engineering</title><title>Biofabrication</title><addtitle>BF</addtitle><addtitle>Biofabrication</addtitle><description>Synthetic small diameter vascular grafts have a high failure rate, and endothelialization is critical for preventing thrombosis and graft occlusion. A promising approach is in situ tissue engineering, whereby an acellular scaffold is implanted and provides stimulatory cues to guide the in situ remodeling into a functional blood vessel. An ideal scaffold should have sufficient binding sites for biomolecule immobilization and a mechanical property similar to native tissue. Here we developed a novel method to blend low molecular weight (LMW) elastic polymer during electrospinning process to increase conjugation sites and to improve the mechanical property of vascular grafts. LMW elastic polymer improved the elasticity of the scaffolds, and significantly increased the amount of heparin conjugated to the micro/nanofibrous scaffolds, which in turn increased the loading capacity of vascular endothelial growth factor (VEGF) and prolonged the release of VEGF. Vascular grafts were implanted into the carotid artery of rats to evaluate the in vivo performance. VEGF treatment significantly enhanced endothelium formation and the overall patency of vascular grafts. Heparin coating also increased cell infiltration into the electrospun grafts, thus increasing the production of collagen and elastin within the graft wall. This work demonstrates that LMW elastic polymer blending is an approach to engineer the mechanical and biological property of micro/nanofibrous vascular grafts for in situ vascular tissue engineering.</description><subject>Animals</subject><subject>Antithrombins - pharmacology</subject><subject>Blood Vessel Prosthesis</subject><subject>Collagen - metabolism</subject><subject>Elastin - metabolism</subject><subject>electrospinning</subject><subject>endothelialization</subject><subject>Endothelium - drug effects</subject><subject>Endothelium - metabolism</subject><subject>Extracellular Matrix - metabolism</subject><subject>heparin</subject><subject>Heparin - pharmacology</subject><subject>Humans</subject><subject>Immobilized Proteins - metabolism</subject><subject>Male</subject><subject>Mechanical Phenomena</subject><subject>Myocytes, Smooth Muscle - metabolism</subject><subject>Nanofibers - chemistry</subject><subject>polycaprolactone</subject><subject>Rats</subject><subject>tissue engineering</subject><subject>Tissue Engineering - methods</subject><subject>Tissue Scaffolds - chemistry</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><subject>vascular endothelial growth factors</subject><subject>vascular grafts</subject><subject>Vascular Patency - drug effects</subject><issn>1758-5090</issn><issn>1758-5082</issn><issn>1758-5090</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUlLxDAUx4MoLqN3T5KLN0dfJ02TXgQRNxC86Dmk6Usn0klK0gril7fj6KggnrK8_wK_R8hhBqcZSHmWCS6nHEo401qyvNogu-uvzR_3HbKX0jNAwXmRbZOdmZSZYDLfJW9XvnEeMTrf0H6OdIFmrr0zuqXa17RyoQ3Nx7OLocPYO0w0WOq1D9ZVMQyJvuhkhlZH2kRt-0RtiNR5mlw_fM96l9KAFL_79smW1W3Cg89zQp6urx4vb6f3Dzd3lxf3U8MB-ikrMC8MMFELW5sqByygFLqwZSGZzmtW8noGnItsxhH0rGKlERIFCGRQSmATcr7K7YZqgbVB30fdqi66hY6vKminfk-8m6smvCguc8HGkgmBVYCJIaWIdu3NQC0XoZak1ZK0Wi1itBz97FwbvsiPgpOVwIVOPYch-hHBf3nHf8grq0rFFLARlFBdbdk7VyiiaQ</recordid><startdate>20170817</startdate><enddate>20170817</enddate><creator>Henry, Jeffrey J D</creator><creator>Yu, Jian</creator><creator>Wang, Aijun</creator><creator>Lee, Randall</creator><creator>Fang, Jun</creator><creator>Li, Song</creator><general>IOP Publishing</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>5PM</scope></search><sort><creationdate>20170817</creationdate><title>Engineering the mechanical and biological properties of nanofibrous vascular grafts for in situ vascular tissue engineering</title><author>Henry, Jeffrey J D ; Yu, Jian ; Wang, Aijun ; Lee, Randall ; Fang, Jun ; Li, Song</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c500t-36e46c037d7fdcb40e6097a6f9683a4d395d20557125e0a2b39c78e707e309803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Antithrombins - pharmacology</topic><topic>Blood Vessel Prosthesis</topic><topic>Collagen - metabolism</topic><topic>Elastin - metabolism</topic><topic>electrospinning</topic><topic>endothelialization</topic><topic>Endothelium - drug effects</topic><topic>Endothelium - metabolism</topic><topic>Extracellular Matrix - metabolism</topic><topic>heparin</topic><topic>Heparin - pharmacology</topic><topic>Humans</topic><topic>Immobilized Proteins - metabolism</topic><topic>Male</topic><topic>Mechanical Phenomena</topic><topic>Myocytes, Smooth Muscle - metabolism</topic><topic>Nanofibers - chemistry</topic><topic>polycaprolactone</topic><topic>Rats</topic><topic>tissue engineering</topic><topic>Tissue Engineering - methods</topic><topic>Tissue Scaffolds - chemistry</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><topic>vascular endothelial growth factors</topic><topic>vascular grafts</topic><topic>Vascular Patency - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Henry, Jeffrey J D</creatorcontrib><creatorcontrib>Yu, Jian</creatorcontrib><creatorcontrib>Wang, Aijun</creatorcontrib><creatorcontrib>Lee, Randall</creatorcontrib><creatorcontrib>Fang, Jun</creatorcontrib><creatorcontrib>Li, Song</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biofabrication</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Henry, Jeffrey J D</au><au>Yu, Jian</au><au>Wang, Aijun</au><au>Lee, Randall</au><au>Fang, Jun</au><au>Li, Song</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Engineering the mechanical and biological properties of nanofibrous vascular grafts for in situ vascular tissue engineering</atitle><jtitle>Biofabrication</jtitle><stitle>BF</stitle><addtitle>Biofabrication</addtitle><date>2017-08-17</date><risdate>2017</risdate><volume>9</volume><issue>3</issue><spage>035007</spage><epage>035007</epage><pages>035007-035007</pages><issn>1758-5090</issn><issn>1758-5082</issn><eissn>1758-5090</eissn><coden>BIOFCK</coden><abstract>Synthetic small diameter vascular grafts have a high failure rate, and endothelialization is critical for preventing thrombosis and graft occlusion. A promising approach is in situ tissue engineering, whereby an acellular scaffold is implanted and provides stimulatory cues to guide the in situ remodeling into a functional blood vessel. An ideal scaffold should have sufficient binding sites for biomolecule immobilization and a mechanical property similar to native tissue. Here we developed a novel method to blend low molecular weight (LMW) elastic polymer during electrospinning process to increase conjugation sites and to improve the mechanical property of vascular grafts. LMW elastic polymer improved the elasticity of the scaffolds, and significantly increased the amount of heparin conjugated to the micro/nanofibrous scaffolds, which in turn increased the loading capacity of vascular endothelial growth factor (VEGF) and prolonged the release of VEGF. Vascular grafts were implanted into the carotid artery of rats to evaluate the in vivo performance. VEGF treatment significantly enhanced endothelium formation and the overall patency of vascular grafts. Heparin coating also increased cell infiltration into the electrospun grafts, thus increasing the production of collagen and elastin within the graft wall. This work demonstrates that LMW elastic polymer blending is an approach to engineer the mechanical and biological property of micro/nanofibrous vascular grafts for in situ vascular tissue engineering.</abstract><cop>England</cop><pub>IOP Publishing</pub><pmid>28817384</pmid><doi>10.1088/1758-5090/aa834b</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antithrombins - pharmacology Blood Vessel Prosthesis Collagen - metabolism Elastin - metabolism electrospinning endothelialization Endothelium - drug effects Endothelium - metabolism Extracellular Matrix - metabolism heparin Heparin - pharmacology Humans Immobilized Proteins - metabolism Male Mechanical Phenomena Myocytes, Smooth Muscle - metabolism Nanofibers - chemistry polycaprolactone Rats tissue engineering Tissue Engineering - methods Tissue Scaffolds - chemistry Vascular Endothelial Growth Factor A - metabolism vascular endothelial growth factors vascular grafts Vascular Patency - drug effects |
title | Engineering the mechanical and biological properties of nanofibrous vascular grafts for in situ vascular tissue engineering |
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