TY - JOUR
T1 - Successful in vitro expansion and differentiation of cord blood derived CD34+ cells into early endothelial progenitor cells reveals highly differential gene expression
AU - Ahrens, Ingo
AU - Domeij, Helena
AU - Topcic, Denijal
AU - Haviv, Izhak
AU - Merivirta, Ruusu-Maaria
AU - Agrotis, Alex
AU - Leitner, Ephraem
AU - Jowett, Jeremy B
AU - Bode, Christoph
AU - Lappas, Martha
AU - Peter, Karlheinz
PY - 2011
Y1 - 2011
N2 - Endothelial progenitor cells (EPCs) can be purified from peripheral blood, bone marrow or cord blood and are typically
defined by a limited number of cell surface markers and a few functional tests. A detailed in vitro characterization is often
restricted by the low cell numbers of circulating EPCs. Therefore in vitro culturing and expansion methods are applied,
which allow at least distinguishing two different types of EPCs, early and late EPCs. Herein, we describe an in vitro culture technique with the aim to generate high numbers of phenotypically, functionally and genetically defined early EPCs from human cord blood. Characterization of EPCs was done by flow cytometry, immunofluorescence microscopy, colony forming unit (CFU) assay and endothelial tube formation assay.
AB - Endothelial progenitor cells (EPCs) can be purified from peripheral blood, bone marrow or cord blood and are typically
defined by a limited number of cell surface markers and a few functional tests. A detailed in vitro characterization is often
restricted by the low cell numbers of circulating EPCs. Therefore in vitro culturing and expansion methods are applied,
which allow at least distinguishing two different types of EPCs, early and late EPCs. Herein, we describe an in vitro culture technique with the aim to generate high numbers of phenotypically, functionally and genetically defined early EPCs from human cord blood. Characterization of EPCs was done by flow cytometry, immunofluorescence microscopy, colony forming unit (CFU) assay and endothelial tube formation assay.
UR - http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0023210
U2 - 10.1371/journal.pone.0023210
DO - 10.1371/journal.pone.0023210
M3 - Article
VL - 6
JO - PLoS ONE
JF - PLoS ONE
SN - 1932-6203
IS - 8
M1 - e23210
ER -