Direct Comparison of Umbilical Cord Blood versus Bone Marrow Derived Endothelial Precursor Cells in Mediating Neovascularization in Response to Vascular Ischemia

Lade...
Vorschaubild
Dateien
Finney_et_al._2006.pdf
Finney_et_al._2006.pdfGröße: 375.49 KBDownloads: 383
Datum
2006
Autor:innen
Finney, Marcie R.
Greco, Nicholas J.
Haynesworth, Stephen E.
Martin, Joseph M.
Hedrick, David P.
Swan, Jimmy Z.
Winter, Daniel G.
Joseph, Matthew E.
Fu, Pingfu
Herausgeber:innen
Kontakt
ISSN der Zeitschrift
Electronic ISSN
ISBN
Bibliografische Daten
Verlag
Schriftenreihe
Auflagebezeichnung
ArXiv-ID
Internationale Patentnummer
Angaben zur Forschungsförderung
Projekt
Open Access-Veröffentlichung
Open Access Green
Sammlungen
Core Facility der Universität Konstanz
Gesperrt bis
Titel in einer weiteren Sprache
Forschungsvorhaben
Organisationseinheiten
Zeitschriftenheft
Publikationstyp
Zeitschriftenartikel
Publikationsstatus
Published
Erschienen in
Biology of Blood and Marrow Transplantation. 2006, 12(5), pp. 585-593. ISSN 1083-8791. Available under: doi: 10.1016/j.bbmt.2005.12.037
Zusammenfassung

Endothelial precursor cells (EPCs) cultured from adult bone marrow (BM) have been shown to mediate neovasculogenesis in murine models of vascular injury. We sought to directly compare umbilical cord blood (UCB)- and BM-derived EPC surface phenotypes and in vivo functional capacity. UCB and BM EPCs derived from mononuclear cells (MNC) were phenotyped by surface staining for expression of stromal (Stro-1, CXCR4, CD105, and CD73), endothelial (CD31, CD146, and vascular endothelial [VE]-cadherin), stem cell (CD34 and CD133), and monocyte (CD14) surface markers and analyzed by flow cytometry. The nonobese diabetic/severe combined immunodeficiency murine model of hind-limb ischemia was used to analyze the potential of MNCs and culturederived EPCs from UCB and BM to mediate neovasculogenesis. Histologic evaluation of the in vivo studies included capillary density as a measure of eovascularization. Surface CXCR4 expression was notably higher on UCB-derived EPCs (64.29% ± 7.41%) compared with BM (19.69% ± 5.49%; P = .021). Although the 2 sources of EPCs were comparable in expression of endothelial and monocyte markers, BM-derived EPCs contained higher proportions of cells expressing stromal cell markers (CD105 and CD73). Injection of UCB- or BM-derived EPCs resulted in significantly improved perfusion as measured by laser Doppler imaging at days 7 and 14 after femoral artery ligation in nonobese diabetic/severe combined immunodeficiency mice compared with controls (P < .05). Injection of uncultured MNCs from BM or UCB showed no significant difference from control mice (P = .119; P = .177). Tissue samples harvested from the lower calf muscle at day 28 demonstrated increased capillary densities in mice receiving BM- or UCB-derived EPCs. In conclusion, we found that UCB and BM-derived EPCs differ in CXCR4 expression and stromal surface markers but mediate equivalent neovasculogenesis in vivo as measured by Doppler flow and histologic analyses.

Zusammenfassung in einer weiteren Sprache
Fachgebiet (DDC)
570 Biowissenschaften, Biologie
Schlagwörter
Umbilical cord blood, Endothelial precursor cells, Neovascularization, Vascular ischemia
Konferenz
Rezension
undefined / . - undefined, undefined
Zitieren
ISO 690FINNEY, Marcie R., Nicholas J. GRECO, Stephen E. HAYNESWORTH, Joseph M. MARTIN, David P. HEDRICK, Jimmy Z. SWAN, Daniel G. WINTER, Suzanne KADEREIT, Matthew E. JOSEPH, Pingfu FU, Vincent J. POMPILI, Mary J. LAUGHLIN, 2006. Direct Comparison of Umbilical Cord Blood versus Bone Marrow Derived Endothelial Precursor Cells in Mediating Neovascularization in Response to Vascular Ischemia. In: Biology of Blood and Marrow Transplantation. 2006, 12(5), pp. 585-593. ISSN 1083-8791. Available under: doi: 10.1016/j.bbmt.2005.12.037
BibTex
@article{Finney2006Direc-8126,
  year={2006},
  doi={10.1016/j.bbmt.2005.12.037},
  title={Direct Comparison of Umbilical Cord Blood versus Bone Marrow Derived Endothelial Precursor Cells in Mediating Neovascularization in Response to Vascular Ischemia},
  number={5},
  volume={12},
  issn={1083-8791},
  journal={Biology of Blood and Marrow Transplantation},
  pages={585--593},
  author={Finney, Marcie R. and Greco, Nicholas J. and Haynesworth, Stephen E. and Martin, Joseph M. and Hedrick, David P. and Swan, Jimmy Z. and Winter, Daniel G. and Kadereit, Suzanne and Joseph, Matthew E. and Fu, Pingfu and Pompili, Vincent J. and Laughlin, Mary J.}
}
RDF
<rdf:RDF
    xmlns:dcterms="http://purl.org/dc/terms/"
    xmlns:dc="http://purl.org/dc/elements/1.1/"
    xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
    xmlns:bibo="http://purl.org/ontology/bibo/"
    xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#"
    xmlns:foaf="http://xmlns.com/foaf/0.1/"
    xmlns:void="http://rdfs.org/ns/void#"
    xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > 
  <rdf:Description rdf:about="https://kops.uni-konstanz.de/server/rdf/resource/123456789/8126">
    <dc:contributor>Hedrick, David P.</dc:contributor>
    <dc:contributor>Winter, Daniel G.</dc:contributor>
    <dc:creator>Haynesworth, Stephen E.</dc:creator>
    <dc:contributor>Laughlin, Mary J.</dc:contributor>
    <dcterms:hasPart rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/8126/1/Finney_et_al._2006.pdf"/>
    <dc:creator>Hedrick, David P.</dc:creator>
    <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/>
    <dc:creator>Kadereit, Suzanne</dc:creator>
    <dc:contributor>Kadereit, Suzanne</dc:contributor>
    <dc:contributor>Finney, Marcie R.</dc:contributor>
    <dcterms:rights rdf:resource="https://rightsstatements.org/page/InC/1.0/"/>
    <dc:rights>terms-of-use</dc:rights>
    <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-24T17:40:49Z</dc:date>
    <foaf:homepage rdf:resource="http://localhost:8080/"/>
    <dc:contributor>Fu, Pingfu</dc:contributor>
    <dcterms:bibliographicCitation>First publ. in: Biology of Blood and Marrow Transplantation 12 (2006), 5, pp. 585-593</dcterms:bibliographicCitation>
    <dcterms:issued>2006</dcterms:issued>
    <dc:contributor>Greco, Nicholas J.</dc:contributor>
    <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/8126"/>
    <dcterms:abstract xml:lang="eng">Endothelial precursor cells (EPCs) cultured from adult bone marrow (BM) have been shown to mediate neovasculogenesis in murine models of vascular injury. We sought to directly compare umbilical cord blood (UCB)- and BM-derived EPC surface phenotypes and in vivo functional capacity. UCB and BM EPCs derived from mononuclear cells (MNC) were phenotyped by surface staining for expression of stromal (Stro-1, CXCR4, CD105, and CD73), endothelial (CD31, CD146, and vascular endothelial [VE]-cadherin), stem cell (CD34 and CD133), and monocyte (CD14) surface markers and analyzed by flow cytometry. The nonobese diabetic/severe combined immunodeficiency murine model of hind-limb ischemia was used to analyze the potential of MNCs and culturederived EPCs from UCB and BM to mediate neovasculogenesis. Histologic evaluation of the in vivo studies included capillary density as a measure of eovascularization. Surface CXCR4 expression was notably higher on UCB-derived EPCs (64.29% ± 7.41%) compared with BM (19.69% ± 5.49%; P = .021). Although the 2 sources of EPCs were comparable in expression of endothelial and monocyte markers, BM-derived EPCs contained higher proportions of cells expressing stromal cell markers (CD105 and CD73). Injection of UCB- or BM-derived EPCs resulted in significantly improved perfusion as measured by laser Doppler imaging at days 7 and 14 after femoral artery ligation in nonobese  diabetic/severe combined immunodeficiency mice compared with controls (P &lt; .05). Injection of uncultured MNCs from BM or UCB showed no significant difference from control mice (P = .119; P = .177). Tissue samples harvested from the lower calf muscle at day 28 demonstrated increased capillary densities in mice receiving BM- or UCB-derived EPCs. In conclusion, we found that UCB and BM-derived EPCs differ in CXCR4 expression and stromal surface markers but mediate equivalent neovasculogenesis in vivo as measured by Doppler flow and histologic analyses.</dcterms:abstract>
    <dc:creator>Winter, Daniel G.</dc:creator>
    <dc:creator>Swan, Jimmy Z.</dc:creator>
    <dc:creator>Fu, Pingfu</dc:creator>
    <dc:contributor>Martin, Joseph M.</dc:contributor>
    <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/>
    <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/>
    <dc:creator>Laughlin, Mary J.</dc:creator>
    <dc:creator>Greco, Nicholas J.</dc:creator>
    <dc:contributor>Haynesworth, Stephen E.</dc:contributor>
    <dc:contributor>Pompili, Vincent J.</dc:contributor>
    <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-24T17:40:49Z</dcterms:available>
    <dcterms:title>Direct Comparison of Umbilical Cord Blood versus Bone Marrow Derived Endothelial Precursor Cells in Mediating Neovascularization in Response to Vascular Ischemia</dcterms:title>
    <dc:creator>Martin, Joseph M.</dc:creator>
    <dspace:hasBitstream rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/8126/1/Finney_et_al._2006.pdf"/>
    <dc:contributor>Swan, Jimmy Z.</dc:contributor>
    <dc:contributor>Joseph, Matthew E.</dc:contributor>
    <dc:creator>Finney, Marcie R.</dc:creator>
    <dc:creator>Joseph, Matthew E.</dc:creator>
    <dc:creator>Pompili, Vincent J.</dc:creator>
    <dc:language>eng</dc:language>
    <dc:format>application/pdf</dc:format>
  </rdf:Description>
</rdf:RDF>
Interner Vermerk
xmlui.Submission.submit.DescribeStep.inputForms.label.kops_note_fromSubmitter
Kontakt
URL der Originalveröffentl.
Prüfdatum der URL
Prüfungsdatum der Dissertation
Finanzierungsart
Kommentar zur Publikation
Allianzlizenz
Corresponding Authors der Uni Konstanz vorhanden
Internationale Co-Autor:innen
Universitätsbibliographie
Nein
Begutachtet
Diese Publikation teilen