Flow with variable pulse frequencies accelerates vascular recellularization and remodeling of a human bioscaffold
Despite significant advances in vascular tissue engineering, the ideal graft has not yet been developed and autologous vessels remain the gold standard substitutes for small diameter bypass procedures. Here, we explore the use of a flow field with variable pulse frequencies over the regeneration of...
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Veröffentlicht in: | Journal of biomedical materials research. Part A 2021-01, Vol.109 (1), p.92-103 |
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description | Despite significant advances in vascular tissue engineering, the ideal graft has not yet been developed and autologous vessels remain the gold standard substitutes for small diameter bypass procedures. Here, we explore the use of a flow field with variable pulse frequencies over the regeneration of an ex vivo‐derived human scaffold as vascular graft. Briefly, human umbilical veins were decellularized and used as scaffold for cellular repopulation with human smooth muscle cells (SMC) and endothelial cells (EC). Over graft development, the variable flow, which mimics the real‐time cardiac output of an individual performing daily activities (e.g., resting vs. exercising), was implemented and compared to the commonly used constant pulse frequency. Results show marked differences on SMC and EC function, with changes at the molecular level reflecting on tissue scales. First, variable frequencies significantly increased SMC proliferation rate and glycosaminoglycan production. These results can be tied with the SMC gene expression that indicates a synthetic phenotype, with a significant downregulation of myosin heavy chain. Additionally and quite remarkably, the variable flow frequencies motivated the re‐endothelialization of the grafts, with a quiescent‐like structure observed after 10 days of conditioning, contrasting with the low surface coverage and unaligned EC observed under constant frequency (CF). Besides, the overall biomechanics of the generated grafts (conditioned with both pulsed and CFs) evidence a significant remodeling after 55 days of culture, depicted by high burst pressure and Young's modulus. These last results demonstrate the positive recellularization and remodeling of a human‐derived scaffold toward an arterial vessel. |
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Here, we explore the use of a flow field with variable pulse frequencies over the regeneration of an ex vivo‐derived human scaffold as vascular graft. Briefly, human umbilical veins were decellularized and used as scaffold for cellular repopulation with human smooth muscle cells (SMC) and endothelial cells (EC). Over graft development, the variable flow, which mimics the real‐time cardiac output of an individual performing daily activities (e.g., resting vs. exercising), was implemented and compared to the commonly used constant pulse frequency. Results show marked differences on SMC and EC function, with changes at the molecular level reflecting on tissue scales. First, variable frequencies significantly increased SMC proliferation rate and glycosaminoglycan production. These results can be tied with the SMC gene expression that indicates a synthetic phenotype, with a significant downregulation of myosin heavy chain. Additionally and quite remarkably, the variable flow frequencies motivated the re‐endothelialization of the grafts, with a quiescent‐like structure observed after 10 days of conditioning, contrasting with the low surface coverage and unaligned EC observed under constant frequency (CF). Besides, the overall biomechanics of the generated grafts (conditioned with both pulsed and CFs) evidence a significant remodeling after 55 days of culture, depicted by high burst pressure and Young's modulus. These last results demonstrate the positive recellularization and remodeling of a human‐derived scaffold toward an arterial vessel.</description><identifier>ISSN: 1549-3296</identifier><identifier>EISSN: 1552-4965</identifier><identifier>DOI: 10.1002/jbm.a.37009</identifier><identifier>PMID: 32441862</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Autografts ; Bioengineering ; biomechanical stimulation ; Biomechanics ; Blood vessels ; Blood Vessels - cytology ; Cardiac Output ; Cardiology and cardiovascular system ; Cell culture ; Cell Proliferation ; Cells, Cultured ; Conditioning ; decellularized human scaffold ; Endothelial Cells ; Engineering Sciences ; Exercise ; Female ; Gene expression ; Glycosaminoglycans ; Glycosaminoglycans - biosynthesis ; Grafting ; Heart ; Heart Rate ; Human health and pathology ; Humans ; Life Sciences ; Mechanical Phenomena ; Mechanical properties ; Mechanics ; Modulus of elasticity ; Muscles ; Myocytes, Smooth Muscle ; Myosin ; Myosin Heavy Chains - biosynthesis ; Phenotypes ; Regeneration ; Repopulation ; Rest ; Scaffolds ; Smc gene ; Smooth muscle ; Tissue Engineering ; Tissue Scaffolds ; Umbilical Arteries - cytology ; Umbilical Veins - cytology ; Vascular Grafting ; Vascular tissue ; vascular tissue engineering</subject><ispartof>Journal of biomedical materials research. 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Part A</title><addtitle>J Biomed Mater Res A</addtitle><description>Despite significant advances in vascular tissue engineering, the ideal graft has not yet been developed and autologous vessels remain the gold standard substitutes for small diameter bypass procedures. Here, we explore the use of a flow field with variable pulse frequencies over the regeneration of an ex vivo‐derived human scaffold as vascular graft. Briefly, human umbilical veins were decellularized and used as scaffold for cellular repopulation with human smooth muscle cells (SMC) and endothelial cells (EC). Over graft development, the variable flow, which mimics the real‐time cardiac output of an individual performing daily activities (e.g., resting vs. exercising), was implemented and compared to the commonly used constant pulse frequency. Results show marked differences on SMC and EC function, with changes at the molecular level reflecting on tissue scales. First, variable frequencies significantly increased SMC proliferation rate and glycosaminoglycan production. These results can be tied with the SMC gene expression that indicates a synthetic phenotype, with a significant downregulation of myosin heavy chain. Additionally and quite remarkably, the variable flow frequencies motivated the re‐endothelialization of the grafts, with a quiescent‐like structure observed after 10 days of conditioning, contrasting with the low surface coverage and unaligned EC observed under constant frequency (CF). Besides, the overall biomechanics of the generated grafts (conditioned with both pulsed and CFs) evidence a significant remodeling after 55 days of culture, depicted by high burst pressure and Young's modulus. These last results demonstrate the positive recellularization and remodeling of a human‐derived scaffold toward an arterial vessel.</description><subject>Autografts</subject><subject>Bioengineering</subject><subject>biomechanical stimulation</subject><subject>Biomechanics</subject><subject>Blood vessels</subject><subject>Blood Vessels - cytology</subject><subject>Cardiac Output</subject><subject>Cardiology and cardiovascular system</subject><subject>Cell culture</subject><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>Conditioning</subject><subject>decellularized human scaffold</subject><subject>Endothelial Cells</subject><subject>Engineering Sciences</subject><subject>Exercise</subject><subject>Female</subject><subject>Gene expression</subject><subject>Glycosaminoglycans</subject><subject>Glycosaminoglycans - biosynthesis</subject><subject>Grafting</subject><subject>Heart</subject><subject>Heart Rate</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Mechanical Phenomena</subject><subject>Mechanical properties</subject><subject>Mechanics</subject><subject>Modulus of elasticity</subject><subject>Muscles</subject><subject>Myocytes, Smooth Muscle</subject><subject>Myosin</subject><subject>Myosin Heavy Chains - biosynthesis</subject><subject>Phenotypes</subject><subject>Regeneration</subject><subject>Repopulation</subject><subject>Rest</subject><subject>Scaffolds</subject><subject>Smc gene</subject><subject>Smooth muscle</subject><subject>Tissue Engineering</subject><subject>Tissue Scaffolds</subject><subject>Umbilical Arteries - cytology</subject><subject>Umbilical Veins - cytology</subject><subject>Vascular Grafting</subject><subject>Vascular tissue</subject><subject>vascular tissue engineering</subject><issn>1549-3296</issn><issn>1552-4965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kctv1DAYxC1ERR9w4o4scaFCu_gR28lxqfoALeICZ-uL7bBeOfHW3uyq_PU4pPTAoSePRj-Nv9Eg9JaSJSWEfdq2_RKWXBHSvEBnVAi2qBopXk66ahacNfIUnee8LbAkgr1Cp5xVFa0lO0P3NyEe8dHvN_gAyUMbHN6NITvcJXc_usF4lzEY44JLsC_6ANmMARJOrphhkv437H0cMAy2uH20LvjhF44dBrwZexhw62M20HUx2NfopIPywZvH9wL9vLn-cXW3WH-__XK1Wi8Mb8rZlXWSyxacVbwWitmuYa0gFFQlOiYVN4aSllvbWdWomru6VY2toZRsgVDDL9DlnLuBoHfJ95AedASv71ZrPXmE1xUTsjrQwn6Y2V2KpXTe697nqR0MLo5Zs4pITpRgsqDv_0O3cUxDaVIoyYUUshaF-jhTJsWck-ueLqBET6vpspoG_Xe1Qr97zBzb3tkn9t9MBWAzcPTBPTyXpb9-_raaU_8Afmai7g</recordid><startdate>202101</startdate><enddate>202101</enddate><creator>Van de Walle, Aurore B.</creator><creator>McFetridge, Peter S.</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><general>Wiley</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>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0003-1579-9145</orcidid></search><sort><creationdate>202101</creationdate><title>Flow with variable pulse frequencies accelerates vascular recellularization and remodeling of a human bioscaffold</title><author>Van de Walle, Aurore B. ; McFetridge, Peter S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3949-4de636baed738572df92b501a745f2673cc10b3ddfd79783e8b79d8a002ba01c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Autografts</topic><topic>Bioengineering</topic><topic>biomechanical stimulation</topic><topic>Biomechanics</topic><topic>Blood vessels</topic><topic>Blood Vessels - cytology</topic><topic>Cardiac Output</topic><topic>Cardiology and cardiovascular system</topic><topic>Cell culture</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>Conditioning</topic><topic>decellularized human scaffold</topic><topic>Endothelial Cells</topic><topic>Engineering Sciences</topic><topic>Exercise</topic><topic>Female</topic><topic>Gene expression</topic><topic>Glycosaminoglycans</topic><topic>Glycosaminoglycans - biosynthesis</topic><topic>Grafting</topic><topic>Heart</topic><topic>Heart Rate</topic><topic>Human health and pathology</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Mechanical Phenomena</topic><topic>Mechanical properties</topic><topic>Mechanics</topic><topic>Modulus of elasticity</topic><topic>Muscles</topic><topic>Myocytes, Smooth Muscle</topic><topic>Myosin</topic><topic>Myosin Heavy Chains - biosynthesis</topic><topic>Phenotypes</topic><topic>Regeneration</topic><topic>Repopulation</topic><topic>Rest</topic><topic>Scaffolds</topic><topic>Smc gene</topic><topic>Smooth muscle</topic><topic>Tissue Engineering</topic><topic>Tissue Scaffolds</topic><topic>Umbilical Arteries - cytology</topic><topic>Umbilical Veins - cytology</topic><topic>Vascular Grafting</topic><topic>Vascular tissue</topic><topic>vascular tissue engineering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Van de Walle, Aurore B.</creatorcontrib><creatorcontrib>McFetridge, Peter S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Journal of biomedical materials research. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Van de Walle, Aurore B.</au><au>McFetridge, Peter S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Flow with variable pulse frequencies accelerates vascular recellularization and remodeling of a human bioscaffold</atitle><jtitle>Journal of biomedical materials research. Part A</jtitle><addtitle>J Biomed Mater Res A</addtitle><date>2021-01</date><risdate>2021</risdate><volume>109</volume><issue>1</issue><spage>92</spage><epage>103</epage><pages>92-103</pages><issn>1549-3296</issn><eissn>1552-4965</eissn><abstract>Despite significant advances in vascular tissue engineering, the ideal graft has not yet been developed and autologous vessels remain the gold standard substitutes for small diameter bypass procedures. Here, we explore the use of a flow field with variable pulse frequencies over the regeneration of an ex vivo‐derived human scaffold as vascular graft. Briefly, human umbilical veins were decellularized and used as scaffold for cellular repopulation with human smooth muscle cells (SMC) and endothelial cells (EC). Over graft development, the variable flow, which mimics the real‐time cardiac output of an individual performing daily activities (e.g., resting vs. exercising), was implemented and compared to the commonly used constant pulse frequency. Results show marked differences on SMC and EC function, with changes at the molecular level reflecting on tissue scales. First, variable frequencies significantly increased SMC proliferation rate and glycosaminoglycan production. These results can be tied with the SMC gene expression that indicates a synthetic phenotype, with a significant downregulation of myosin heavy chain. Additionally and quite remarkably, the variable flow frequencies motivated the re‐endothelialization of the grafts, with a quiescent‐like structure observed after 10 days of conditioning, contrasting with the low surface coverage and unaligned EC observed under constant frequency (CF). Besides, the overall biomechanics of the generated grafts (conditioned with both pulsed and CFs) evidence a significant remodeling after 55 days of culture, depicted by high burst pressure and Young's modulus. These last results demonstrate the positive recellularization and remodeling of a human‐derived scaffold toward an arterial vessel.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>32441862</pmid><doi>10.1002/jbm.a.37009</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-1579-9145</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Autografts Bioengineering biomechanical stimulation Biomechanics Blood vessels Blood Vessels - cytology Cardiac Output Cardiology and cardiovascular system Cell culture Cell Proliferation Cells, Cultured Conditioning decellularized human scaffold Endothelial Cells Engineering Sciences Exercise Female Gene expression Glycosaminoglycans Glycosaminoglycans - biosynthesis Grafting Heart Heart Rate Human health and pathology Humans Life Sciences Mechanical Phenomena Mechanical properties Mechanics Modulus of elasticity Muscles Myocytes, Smooth Muscle Myosin Myosin Heavy Chains - biosynthesis Phenotypes Regeneration Repopulation Rest Scaffolds Smc gene Smooth muscle Tissue Engineering Tissue Scaffolds Umbilical Arteries - cytology Umbilical Veins - cytology Vascular Grafting Vascular tissue vascular tissue engineering |
title | Flow with variable pulse frequencies accelerates vascular recellularization and remodeling of a human bioscaffold |
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