Design and Characterization of an Injectable Pericardial Matrix Gel: A Potentially Autologous Scaffold for Cardiac Tissue Engineering
Following ischemic injury in the heart, little to no repair occurs, causing a progressive degeneration of cardiac function that leads to congestive heart failure. Cardiac tissue engineering strategies have focused on designing a variety of injectable scaffolds that range in composition from single-c...
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Veröffentlicht in: | Tissue engineering. Part A 2010-06, Vol.16 (6), p.217-2027 |
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creator | Seif-Naraghi, Sonya B. Salvatore, Michael A. Schup-Magoffin, Pam J. Hu, Diane P. Christman, Karen L. |
description | Following ischemic injury in the heart, little to no repair occurs, causing a progressive degeneration of cardiac function that leads to congestive heart failure. Cardiac tissue engineering strategies have focused on designing a variety of injectable scaffolds that range in composition from single-component materials to complex extracellular matrix (ECM)–derived materials. In this study, the pericardial ECM, a commonly used biomaterial, was investigated for use as an injectable scaffold for cardiac repair. It was determined that a solubilized form of decellularized porcine pericardium could be injected and induced to gel
in vivo
, prompting investigation with human pericardium, which has the decided advantage of offering an autologous therapy. Characterization showed that the matrix gels retained components of the native pericardial ECM, with extant protein and glycosaminoglycan content identified. The results of an
in vitro
migration assay indicate that the porcine pericardial matrix is a stronger chemoattractant for relevant cell types, but
in vivo
results showed that the two materials caused statistically similar amounts of neovascularization, demonstrating feasibility as injectable treatments. Potential stem cell mobilization was supported by the presence of c-Kit+ cells within the matrix injection regions. With this work, the pericardium is identified as a novel source for an autologous scaffold for treating myocardial infarction. |
doi_str_mv | 10.1089/ten.tea.2009.0768 |
format | Article |
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in vivo
, prompting investigation with human pericardium, which has the decided advantage of offering an autologous therapy. Characterization showed that the matrix gels retained components of the native pericardial ECM, with extant protein and glycosaminoglycan content identified. The results of an
in vitro
migration assay indicate that the porcine pericardial matrix is a stronger chemoattractant for relevant cell types, but
in vivo
results showed that the two materials caused statistically similar amounts of neovascularization, demonstrating feasibility as injectable treatments. Potential stem cell mobilization was supported by the presence of c-Kit+ cells within the matrix injection regions. With this work, the pericardium is identified as a novel source for an autologous scaffold for treating myocardial infarction.</description><identifier>ISSN: 1937-3341</identifier><identifier>EISSN: 1937-335X</identifier><identifier>DOI: 10.1089/ten.tea.2009.0768</identifier><identifier>PMID: 20100033</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc</publisher><subject>Animals ; Biomedical materials ; Care and treatment ; Cell Movement - physiology ; Cells, Cultured ; Cellular biology ; Extracellular matrix ; Extracellular Matrix - chemistry ; Gels - chemistry ; Heart ; Heart attacks ; Heart diseases ; Humans ; Immunohistochemistry ; Injections ; Original ; Original Articles ; Pericardium - chemistry ; Physiological aspects ; Rats ; Stem cells ; Swine ; Tissue engineering ; Tissue Engineering - methods ; Tissue Scaffolds - chemistry</subject><ispartof>Tissue engineering. Part A, 2010-06, Vol.16 (6), p.217-2027</ispartof><rights>2010, Mary Ann Liebert, Inc.</rights><rights>COPYRIGHT 2010 Mary Ann Liebert, Inc.</rights><rights>(©) Copyright 2010, Mary Ann Liebert, Inc.</rights><rights>Copyright 2010, Mary Ann Liebert, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c686t-bac83b034f727faef1cff943f518ffbce0121c9cd79dece4dfafc92e1d9343973</citedby><cites>FETCH-LOGICAL-c686t-bac83b034f727faef1cff943f518ffbce0121c9cd79dece4dfafc92e1d9343973</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.liebertpub.com/doi/epdf/10.1089/ten.tea.2009.0768$$EPDF$$P50$$Gmaryannliebert$$H</linktopdf><linktohtml>$$Uhttps://www.liebertpub.com/doi/full/10.1089/ten.tea.2009.0768$$EHTML$$P50$$Gmaryannliebert$$H</linktohtml><link.rule.ids>230,314,776,780,881,3029,21702,27901,27902,55266,55278</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20100033$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Seif-Naraghi, Sonya B.</creatorcontrib><creatorcontrib>Salvatore, Michael A.</creatorcontrib><creatorcontrib>Schup-Magoffin, Pam J.</creatorcontrib><creatorcontrib>Hu, Diane P.</creatorcontrib><creatorcontrib>Christman, Karen L.</creatorcontrib><title>Design and Characterization of an Injectable Pericardial Matrix Gel: A Potentially Autologous Scaffold for Cardiac Tissue Engineering</title><title>Tissue engineering. Part A</title><addtitle>Tissue Eng Part A</addtitle><description>Following ischemic injury in the heart, little to no repair occurs, causing a progressive degeneration of cardiac function that leads to congestive heart failure. Cardiac tissue engineering strategies have focused on designing a variety of injectable scaffolds that range in composition from single-component materials to complex extracellular matrix (ECM)–derived materials. In this study, the pericardial ECM, a commonly used biomaterial, was investigated for use as an injectable scaffold for cardiac repair. It was determined that a solubilized form of decellularized porcine pericardium could be injected and induced to gel
in vivo
, prompting investigation with human pericardium, which has the decided advantage of offering an autologous therapy. Characterization showed that the matrix gels retained components of the native pericardial ECM, with extant protein and glycosaminoglycan content identified. The results of an
in vitro
migration assay indicate that the porcine pericardial matrix is a stronger chemoattractant for relevant cell types, but
in vivo
results showed that the two materials caused statistically similar amounts of neovascularization, demonstrating feasibility as injectable treatments. Potential stem cell mobilization was supported by the presence of c-Kit+ cells within the matrix injection regions. With this work, the pericardium is identified as a novel source for an autologous scaffold for treating myocardial infarction.</description><subject>Animals</subject><subject>Biomedical materials</subject><subject>Care and treatment</subject><subject>Cell Movement - physiology</subject><subject>Cells, Cultured</subject><subject>Cellular biology</subject><subject>Extracellular matrix</subject><subject>Extracellular Matrix - chemistry</subject><subject>Gels - chemistry</subject><subject>Heart</subject><subject>Heart attacks</subject><subject>Heart diseases</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Injections</subject><subject>Original</subject><subject>Original Articles</subject><subject>Pericardium - chemistry</subject><subject>Physiological aspects</subject><subject>Rats</subject><subject>Stem cells</subject><subject>Swine</subject><subject>Tissue engineering</subject><subject>Tissue Engineering - methods</subject><subject>Tissue Scaffolds - chemistry</subject><issn>1937-3341</issn><issn>1937-335X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNUtFqFDEUHcRia_UDfJGgDz7tmEyyk4kPwrLWWqhYsIJvIZO5mWbJJm2SEeu7_2222y5WBCWEhHPPOZzc3Kp6RnBNcCdeZ_B1BlU3GIsa87Z7UB0QQfmM0vnXh7s7I_vV45RWGLe45fxRtd9ggjGm9KD6-Q6SHT1SfkDLCxWVzhDtD5Vt8CiYgqMTvwKdVe8AnZWaVnGwyqGPKkf7HR2De4MW6CyUMLng7hotphxcGMOU0GetjAluQCZEtLxRanRuU5oAHfnReiiOfnxS7RnlEjy9PQ-rL--PzpcfZqefjk-Wi9OZbrs2z3qlO9pjygxvuFFgiDZGMGrmpDOm14BJQ7TQAxcDaGCDUUaLBsggKKOC08Pq7db3curXMOgSOSonL6Ndq3gtg7LyfsXbCzmGb7IRTDSEFYNXtwYxXE2QslzbpME55aG8V3I2bxkmBP-bSSkhTcdFYb74g7kKU_SlD3KOWXHkoi2kl1vSqBxI600o-fTGUi4a1jFMu5t49V9YZQ2wtjp4MLbg9wRkK9AxpBTB7HpBsNzMmCzfWraSmxmTmxkrmue_N3GnuBuqQuBbwgZW3jsLPcT8H9a_AJhd4zk</recordid><startdate>20100601</startdate><enddate>20100601</enddate><creator>Seif-Naraghi, Sonya B.</creator><creator>Salvatore, Michael A.</creator><creator>Schup-Magoffin, Pam J.</creator><creator>Hu, Diane P.</creator><creator>Christman, Karen L.</creator><general>Mary Ann Liebert, Inc</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>3V.</scope><scope>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20100601</creationdate><title>Design and Characterization of an Injectable Pericardial Matrix Gel: A Potentially Autologous Scaffold for Cardiac Tissue Engineering</title><author>Seif-Naraghi, Sonya B. ; Salvatore, Michael A. ; Schup-Magoffin, Pam J. ; Hu, Diane P. ; Christman, Karen L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c686t-bac83b034f727faef1cff943f518ffbce0121c9cd79dece4dfafc92e1d9343973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Biomedical materials</topic><topic>Care and treatment</topic><topic>Cell Movement - physiology</topic><topic>Cells, Cultured</topic><topic>Cellular biology</topic><topic>Extracellular matrix</topic><topic>Extracellular Matrix - chemistry</topic><topic>Gels - chemistry</topic><topic>Heart</topic><topic>Heart attacks</topic><topic>Heart diseases</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Injections</topic><topic>Original</topic><topic>Original Articles</topic><topic>Pericardium - chemistry</topic><topic>Physiological aspects</topic><topic>Rats</topic><topic>Stem cells</topic><topic>Swine</topic><topic>Tissue engineering</topic><topic>Tissue Engineering - methods</topic><topic>Tissue Scaffolds - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seif-Naraghi, Sonya B.</creatorcontrib><creatorcontrib>Salvatore, Michael A.</creatorcontrib><creatorcontrib>Schup-Magoffin, Pam J.</creatorcontrib><creatorcontrib>Hu, Diane P.</creatorcontrib><creatorcontrib>Christman, Karen L.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Tissue engineering. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seif-Naraghi, Sonya B.</au><au>Salvatore, Michael A.</au><au>Schup-Magoffin, Pam J.</au><au>Hu, Diane P.</au><au>Christman, Karen L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design and Characterization of an Injectable Pericardial Matrix Gel: A Potentially Autologous Scaffold for Cardiac Tissue Engineering</atitle><jtitle>Tissue engineering. Part A</jtitle><addtitle>Tissue Eng Part A</addtitle><date>2010-06-01</date><risdate>2010</risdate><volume>16</volume><issue>6</issue><spage>217</spage><epage>2027</epage><pages>217-2027</pages><issn>1937-3341</issn><eissn>1937-335X</eissn><abstract>Following ischemic injury in the heart, little to no repair occurs, causing a progressive degeneration of cardiac function that leads to congestive heart failure. Cardiac tissue engineering strategies have focused on designing a variety of injectable scaffolds that range in composition from single-component materials to complex extracellular matrix (ECM)–derived materials. In this study, the pericardial ECM, a commonly used biomaterial, was investigated for use as an injectable scaffold for cardiac repair. It was determined that a solubilized form of decellularized porcine pericardium could be injected and induced to gel
in vivo
, prompting investigation with human pericardium, which has the decided advantage of offering an autologous therapy. Characterization showed that the matrix gels retained components of the native pericardial ECM, with extant protein and glycosaminoglycan content identified. The results of an
in vitro
migration assay indicate that the porcine pericardial matrix is a stronger chemoattractant for relevant cell types, but
in vivo
results showed that the two materials caused statistically similar amounts of neovascularization, demonstrating feasibility as injectable treatments. Potential stem cell mobilization was supported by the presence of c-Kit+ cells within the matrix injection regions. With this work, the pericardium is identified as a novel source for an autologous scaffold for treating myocardial infarction.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc</pub><pmid>20100033</pmid><doi>10.1089/ten.tea.2009.0768</doi><tpages>1811</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biomedical materials Care and treatment Cell Movement - physiology Cells, Cultured Cellular biology Extracellular matrix Extracellular Matrix - chemistry Gels - chemistry Heart Heart attacks Heart diseases Humans Immunohistochemistry Injections Original Original Articles Pericardium - chemistry Physiological aspects Rats Stem cells Swine Tissue engineering Tissue Engineering - methods Tissue Scaffolds - chemistry |
title | Design and Characterization of an Injectable Pericardial Matrix Gel: A Potentially Autologous Scaffold for Cardiac Tissue Engineering |
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