CD34+ cells represent highly functional endothelial progenitor cells in murine bone marrow.

BACKGROUND: Endothelial progenitor cells (EPCs) were shown to have angiogenic potential contributing to neovascularization. However, a clear definition of mouse EPCs by cell surface markers still remains elusive. We hypothesized that CD34 could be used for identification and isolation of functional...

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Main Authors: Junjie Yang, Masaaki Ii, Naosuke Kamei, Cantas Alev, Sang-Mo Kwon, Atsuhiko Kawamoto, Hiroshi Akimaru, Haruchika Masuda, Yoshiki Sawa, Takayuki Asahara
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3105013?pdf=render
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author Junjie Yang
Masaaki Ii
Naosuke Kamei
Cantas Alev
Sang-Mo Kwon
Atsuhiko Kawamoto
Hiroshi Akimaru
Haruchika Masuda
Yoshiki Sawa
Takayuki Asahara
author_facet Junjie Yang
Masaaki Ii
Naosuke Kamei
Cantas Alev
Sang-Mo Kwon
Atsuhiko Kawamoto
Hiroshi Akimaru
Haruchika Masuda
Yoshiki Sawa
Takayuki Asahara
author_sort Junjie Yang
collection DOAJ
description BACKGROUND: Endothelial progenitor cells (EPCs) were shown to have angiogenic potential contributing to neovascularization. However, a clear definition of mouse EPCs by cell surface markers still remains elusive. We hypothesized that CD34 could be used for identification and isolation of functional EPCs from mouse bone marrow. METHODOLOGY/PRINCIPAL FINDINGS: CD34(+) cells, c-Kit(+)/Sca-1(+)/Lin(-) (KSL) cells, c-Kit(+)/Lin(-) (KL) cells and Sca-1(+)/Lin(-) (SL) cells were isolated from mouse bone marrow mononuclear cells (BMMNCs) using fluorescent activated cell sorting. EPC colony forming capacity and differentiation capacity into endothelial lineage were examined in the cells. Although CD34(+) cells showed the lowest EPC colony forming activity, CD34(+) cells exhibited under endothelial culture conditions a more adherent phenotype compared with the others, demonstrating the highest mRNA expression levels of endothelial markers vWF, VE-cadherin, and Flk-1. Furthermore, a dramatic increase in immediate recruitment of cells to the myocardium following myocardial infarction and systemic cell injection was observed for CD34(+) cells comparing with others, which could be explained by the highest mRNA expression levels of key homing-related molecules Integrin β2 and CXCR4 in CD34(+) cells. Cell retention and incorporation into the vasculature of the ischemic myocardium was also markedly increased in the CD34(+) cell-injected group, giving a possible explanation for significant reduction in fibrosis area, significant increase in neovascularization and the best cardiac functional recovery in this group in comparison with the others. CONCLUSION: These findings suggest that mouse CD34(+) cells may represent a functional EPC population in bone marrow, which could benefit the investigation of therapeutic EPC biology.
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spelling doaj.art-4aeca3021cee4338842977456d5e06b92022-12-22T03:58:39ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0165e2021910.1371/journal.pone.0020219CD34+ cells represent highly functional endothelial progenitor cells in murine bone marrow.Junjie YangMasaaki IiNaosuke KameiCantas AlevSang-Mo KwonAtsuhiko KawamotoHiroshi AkimaruHaruchika MasudaYoshiki SawaTakayuki AsaharaBACKGROUND: Endothelial progenitor cells (EPCs) were shown to have angiogenic potential contributing to neovascularization. However, a clear definition of mouse EPCs by cell surface markers still remains elusive. We hypothesized that CD34 could be used for identification and isolation of functional EPCs from mouse bone marrow. METHODOLOGY/PRINCIPAL FINDINGS: CD34(+) cells, c-Kit(+)/Sca-1(+)/Lin(-) (KSL) cells, c-Kit(+)/Lin(-) (KL) cells and Sca-1(+)/Lin(-) (SL) cells were isolated from mouse bone marrow mononuclear cells (BMMNCs) using fluorescent activated cell sorting. EPC colony forming capacity and differentiation capacity into endothelial lineage were examined in the cells. Although CD34(+) cells showed the lowest EPC colony forming activity, CD34(+) cells exhibited under endothelial culture conditions a more adherent phenotype compared with the others, demonstrating the highest mRNA expression levels of endothelial markers vWF, VE-cadherin, and Flk-1. Furthermore, a dramatic increase in immediate recruitment of cells to the myocardium following myocardial infarction and systemic cell injection was observed for CD34(+) cells comparing with others, which could be explained by the highest mRNA expression levels of key homing-related molecules Integrin β2 and CXCR4 in CD34(+) cells. Cell retention and incorporation into the vasculature of the ischemic myocardium was also markedly increased in the CD34(+) cell-injected group, giving a possible explanation for significant reduction in fibrosis area, significant increase in neovascularization and the best cardiac functional recovery in this group in comparison with the others. CONCLUSION: These findings suggest that mouse CD34(+) cells may represent a functional EPC population in bone marrow, which could benefit the investigation of therapeutic EPC biology.http://europepmc.org/articles/PMC3105013?pdf=render
spellingShingle Junjie Yang
Masaaki Ii
Naosuke Kamei
Cantas Alev
Sang-Mo Kwon
Atsuhiko Kawamoto
Hiroshi Akimaru
Haruchika Masuda
Yoshiki Sawa
Takayuki Asahara
CD34+ cells represent highly functional endothelial progenitor cells in murine bone marrow.
PLoS ONE
title CD34+ cells represent highly functional endothelial progenitor cells in murine bone marrow.
title_full CD34+ cells represent highly functional endothelial progenitor cells in murine bone marrow.
title_fullStr CD34+ cells represent highly functional endothelial progenitor cells in murine bone marrow.
title_full_unstemmed CD34+ cells represent highly functional endothelial progenitor cells in murine bone marrow.
title_short CD34+ cells represent highly functional endothelial progenitor cells in murine bone marrow.
title_sort cd34 cells represent highly functional endothelial progenitor cells in murine bone marrow
url http://europepmc.org/articles/PMC3105013?pdf=render
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