Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/14662
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dc.contributor.authorNoseda, M-
dc.contributor.authorHarada, M-
dc.contributor.authorMcSweeney, S-
dc.contributor.authorLeja, T-
dc.contributor.authorBelian, E-
dc.contributor.authorStuckey, DJ-
dc.contributor.authorPaiva, MSA-
dc.contributor.authorHabib, J-
dc.contributor.authorMacaulay, I-
dc.contributor.authorde Smith, AJ-
dc.contributor.authoral-Beidh, F-
dc.contributor.authorSampson, R-
dc.contributor.authorLumbers, RT-
dc.contributor.authorRao, P-
dc.contributor.authorHarding, SE-
dc.contributor.authorBlakemore, AIF-
dc.contributor.authorJacobsen, SE-
dc.contributor.authorBarahona, M-
dc.contributor.authorSchneider, MD-
dc.date.accessioned2017-06-01T15:26:33Z-
dc.date.available2015-05-01-
dc.date.available2017-06-01T15:26:33Z-
dc.date.issued2015-
dc.identifier.citationNATURE COMMUNICATIONS, (2015)en_US
dc.identifier.issnhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000355526900001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=f12c8c83318cf2733e615e54d9ed7ad5-
dc.identifier.issnARTN 6930-
dc.identifier.issnhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000355526900001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=f12c8c83318cf2733e615e54d9ed7ad5-
dc.identifier.issnARTN 6930-
dc.identifier.issn2041-1723-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/14662-
dc.description.abstractCardiac progenitor/stem cells in adult hearts represent an attractive therapeutic target for heart regeneration, though (inter)-relationships among reported cells remain obscure. Using single-cell qRT–PCR and clonal analyses, here we define four subpopulations of cardiac progenitor/stem cells in adult mouse myocardium all sharing stem cell antigen-1 (Sca1), based on side population (SP) phenotype, PECAM-1 (CD31) and platelet-derived growth factor receptor-a (PDGFRa) expression. SP status predicts clonogenicity and cardiogenic gene expression (Gata4/6, Hand2 and Tbx5/20), properties segregating more specifically to PDGFRaþ cells. Clonal progeny of single Sca1þ SP cells show cardiomyocyte, endothelial and smooth muscle lineage potential after cardiac grafting, augmenting cardiac function although durable engraftment is rare. PDGFRa cells are characterized by Kdr/Flk1, Cdh5, CD31 and lack of clonogenicity. PDGFRaþ/CD31 cells derive from cells formerly expressing Mesp1, Nkx2-5, Isl1, Gata5 and Wt1, distinct from PDGFRa /CD31þ cells (Gata5 low; Flk1 and Tie2 high). Thus, PDGFRa demarcates the clonogenic cardiogenic Sca1þ stem/progenitor cell.en_US
dc.format.extent? - ? (16)-
dc.languageEnglish-
dc.language.isoenen_US
dc.publisherNATURE PUBLISHING GROUPen_US
dc.subjectScience & Technologyen_US
dc.subjectMultidisciplinary Sciencesen_US
dc.subjectScience & Technology - Other Topicsen_US
dc.subjectCARDIAC STEM-CELLSen_US
dc.subjectSIDE POPULATION CELLSen_US
dc.subjectPROGENITOR CELLSen_US
dc.subjectSMOOTH-MUSCLEen_US
dc.subjectPRESSURE-OVERLOADen_US
dc.subjectTRANSGENIC MICEen_US
dc.subjectHEART REPAIRen_US
dc.subjectIN-VITROen_US
dc.subjectCARDIOMYOCYTESen_US
dc.subjectREGENERATIONen_US
dc.titlePDGFR alpha demarcates the cardiogenic clonogenic Sca1(+) stem/progenitor cell in adult murine myocardiumen_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.1038/ncomms7930-
dc.relation.isPartOfNATURE COMMUNICATIONS-
pubs.publication-statusPublished-
pubs.volume6-
Appears in Collections:Dept of Life Sciences Research Papers

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