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dc.contributor.authorSales, Virna L.
dc.contributor.authorMettler, Bret A.
dc.contributor.authorEngelmayr, George C.
dc.contributor.authorAikawa, Elena
dc.contributor.authorBischoff, Joyce
dc.contributor.authorMartin, David P.
dc.contributor.authorExarhopoulos, Alexis
dc.contributor.authorMoses, Marsha A.
dc.contributor.authorSchoen, Frederick J.
dc.contributor.authorSacks, Michael S.
dc.contributor.authorMayer, John E.
dc.date.accessioned2011-04-08T16:16:57Z
dc.date.available2011-04-08T16:16:57Z
dc.date.issued2010-01
dc.identifier.issn1937-3341
dc.identifier.issn1937-335X
dc.identifier.urihttp://hdl.handle.net/1721.1/62173
dc.description.abstractPurposes: We investigated whether circulating endothelial progenitor cells (EPCs) can be used as a cell source for the creation of a tissue-engineered heart valve (TEHV). Methods: Trileaflet valved conduits were fabricated using nonwoven polyglycolic acid/poly-4-hydroxybutyrate polymer. Ovine peripheral blood EPCs were dynamically seeded onto a valved conduit and incubated for 7, 14, and 21 days. Results: Before seeding, EPCs were shown to express CD31+, eNOS+, and VE-Cadherin+ but not [alpha]-smooth muscle actin. Histological analysis demonstrated relatively homogenous cellular ingrowth throughout the valved conduit. TEHV constructs revealed the presence of endothelial cell (EC) markers and α-smooth muscle actin+ cells comparable with native valves. Protein levels were comparable with native valves and exceeded those in unseeded controls. EPC-TEHV demonstrated a temporal pattern of matrix metalloproteinases-2/9 expression and tissue inhibitors of metalloproteinase activities comparable to that of native valves. Mechanical properties of EPC-TEHV demonstrated significantly greater stiffness than that of the unseeded scaffolds and native valves. Conclusions: Circulating EPC appears to have the potential to provide both interstitial and endothelial functions and could potentially serve as a single-cell source for construction of autologous heart valves.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (HL-06490)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (HL-60463)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (HL-68816)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (HL-CA83106)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (P01CA45548)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (P50DK065298)en_US
dc.description.sponsorshipNational Institute of Standards and Technology (U.S.)en_US
dc.description.sponsorshipNational Institute of Standards and Technology (U.S.) (grant NANB2H3053)en_US
dc.description.sponsorshipCenter for Integration of Medicine and Innovative Technologyen_US
dc.description.sponsorshipGross Cardiovascular Funden_US
dc.description.sponsorshipAmerican Heart Association (Scientist Development Grant 0635620T)en_US
dc.description.sponsorshipNational Institute of Biomedical Imaging and Bioengineering (U.S.) (grant F32 EB003353-01)en_US
dc.description.sponsorshipRuth L. Kirschstein National Research Service Awarden_US
dc.description.sponsorshipAmerican Heart Association (Predoctoral Fellowship 0415406U)en_US
dc.language.isoen_US
dc.publisherMary Ann Liebert, Inc.en_US
dc.relation.isversionofhttp://dx.doi.org/10.1089/ten.tea.2009.0424en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceMary Ann Lieberten_US
dc.titleEndothelial Progenitor Cells as a Sole Source for Ex Vivo Seeding of Tissue-Engineered Heart Valvesen_US
dc.typeArticleen_US
dc.identifier.citationSales, Virna L. et al. “Endothelial Progenitor Cells as a Sole Source for Ex Vivo Seeding of Tissue-Engineered Heart Valves.” Tissue Engineering Part A 16.1 (2011) : 257-267. ©Mary Ann Liebert, Inc., publishers.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.approverSchoen, Frederick J.
dc.contributor.mitauthorSchoen, Frederick J.
dc.contributor.mitauthorEngelmayr, George C.
dc.relation.journalTissue Engineering. Part Aen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsSales, Virna L.; Mettler, Bret A.; Engelmayr, George C.; Aikawa, Elena; Bischoff, Joyce; Martin, David P.; Exarhopoulos, Alexis; Moses, Marsha A.; Schoen, Frederick J.; Sacks, Michael S.; Mayer, John E.en
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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