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O(2) Level Controls Hematopoietic Circulating Progenitor Cells Differentiation into Endothelial or Smooth Muscle Cells

BACKGROUND: Recent studies showed that progenitor cells could differentiate into mature vascular cells. The main physiological factors implicated in cell differentiation are specific growth factors. We hypothesized that simply by varying the oxygen content, progenitor cells can be differentiated eit...

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Autores principales: Berthelemy, Nicolas, Kerdjoudj, Halima, Schaaf, Pierre, Prin-Mathieu, Christine, Lacolley, Patrick, Stoltz, Jean-François, Voegel, Jean-Claude, Menu, Patrick
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2678195/
https://www.ncbi.nlm.nih.gov/pubmed/19436758
http://dx.doi.org/10.1371/journal.pone.0005514
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author Berthelemy, Nicolas
Kerdjoudj, Halima
Schaaf, Pierre
Prin-Mathieu, Christine
Lacolley, Patrick
Stoltz, Jean-François
Voegel, Jean-Claude
Menu, Patrick
author_facet Berthelemy, Nicolas
Kerdjoudj, Halima
Schaaf, Pierre
Prin-Mathieu, Christine
Lacolley, Patrick
Stoltz, Jean-François
Voegel, Jean-Claude
Menu, Patrick
author_sort Berthelemy, Nicolas
collection PubMed
description BACKGROUND: Recent studies showed that progenitor cells could differentiate into mature vascular cells. The main physiological factors implicated in cell differentiation are specific growth factors. We hypothesized that simply by varying the oxygen content, progenitor cells can be differentiated either in mature endothelial cells (ECs) or contractile smooth muscle cells (SMCs) while keeping exactly the same culture medium. METHODOLOGY/PRINCIPAL FINDINGS: Mononuclear cells were isolated by density gradient were cultivated under hypoxic (5% O(2)) or normoxic (21% O(2)) environment. Differentiated cells characterization was performed by confocal microscopy examination and flow cytometry analyses. The phenotype stability over a longer time period was also performed. The morphological examination of the confluent obtained cells after several weeks (between 2 and 4 weeks) showed two distinct morphologies: cobblestone shape in normoxia and a spindle like shape in hypoxia. The cell characterization showed that cobblestone cells were positive to ECs markers while spindle like shape cells were positive to contractile SMCs markers. Moreover, after several further amplification (until 3(rd) passage) in hypoxic or normoxic conditions of the previously differentiated SMC, immunofluorescence studies showed that more than 80% cells continued to express SMCs markers whatever the cell environmental culture conditions with a higher contractile markers expression compared to control (aorta SMCs) signature of phenotype stability. CONCLUSION/SIGNIFICANCE: We demonstrate in this paper that in vitro culture of peripheral blood mononuclear cells with specific angiogenic growth factors under hypoxic conditions leads to SMCs differentiation into a contractile phenotype, signature of their physiological state. Moreover after amplification, the differentiated SMC did not reverse and keep their contractile phenotype after the 3(rd) passage performed under hypoxic and normoxic conditions. These aspects are of the highest importance for tissue engineering strategies. These results highlight also the determinant role of the tissue environment in the differentiation process of vascular progenitor cells.
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spelling pubmed-26781952009-05-13 O(2) Level Controls Hematopoietic Circulating Progenitor Cells Differentiation into Endothelial or Smooth Muscle Cells Berthelemy, Nicolas Kerdjoudj, Halima Schaaf, Pierre Prin-Mathieu, Christine Lacolley, Patrick Stoltz, Jean-François Voegel, Jean-Claude Menu, Patrick PLoS One Research Article BACKGROUND: Recent studies showed that progenitor cells could differentiate into mature vascular cells. The main physiological factors implicated in cell differentiation are specific growth factors. We hypothesized that simply by varying the oxygen content, progenitor cells can be differentiated either in mature endothelial cells (ECs) or contractile smooth muscle cells (SMCs) while keeping exactly the same culture medium. METHODOLOGY/PRINCIPAL FINDINGS: Mononuclear cells were isolated by density gradient were cultivated under hypoxic (5% O(2)) or normoxic (21% O(2)) environment. Differentiated cells characterization was performed by confocal microscopy examination and flow cytometry analyses. The phenotype stability over a longer time period was also performed. The morphological examination of the confluent obtained cells after several weeks (between 2 and 4 weeks) showed two distinct morphologies: cobblestone shape in normoxia and a spindle like shape in hypoxia. The cell characterization showed that cobblestone cells were positive to ECs markers while spindle like shape cells were positive to contractile SMCs markers. Moreover, after several further amplification (until 3(rd) passage) in hypoxic or normoxic conditions of the previously differentiated SMC, immunofluorescence studies showed that more than 80% cells continued to express SMCs markers whatever the cell environmental culture conditions with a higher contractile markers expression compared to control (aorta SMCs) signature of phenotype stability. CONCLUSION/SIGNIFICANCE: We demonstrate in this paper that in vitro culture of peripheral blood mononuclear cells with specific angiogenic growth factors under hypoxic conditions leads to SMCs differentiation into a contractile phenotype, signature of their physiological state. Moreover after amplification, the differentiated SMC did not reverse and keep their contractile phenotype after the 3(rd) passage performed under hypoxic and normoxic conditions. These aspects are of the highest importance for tissue engineering strategies. These results highlight also the determinant role of the tissue environment in the differentiation process of vascular progenitor cells. Public Library of Science 2009-05-13 /pmc/articles/PMC2678195/ /pubmed/19436758 http://dx.doi.org/10.1371/journal.pone.0005514 Text en Berthelemy et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Berthelemy, Nicolas
Kerdjoudj, Halima
Schaaf, Pierre
Prin-Mathieu, Christine
Lacolley, Patrick
Stoltz, Jean-François
Voegel, Jean-Claude
Menu, Patrick
O(2) Level Controls Hematopoietic Circulating Progenitor Cells Differentiation into Endothelial or Smooth Muscle Cells
title O(2) Level Controls Hematopoietic Circulating Progenitor Cells Differentiation into Endothelial or Smooth Muscle Cells
title_full O(2) Level Controls Hematopoietic Circulating Progenitor Cells Differentiation into Endothelial or Smooth Muscle Cells
title_fullStr O(2) Level Controls Hematopoietic Circulating Progenitor Cells Differentiation into Endothelial or Smooth Muscle Cells
title_full_unstemmed O(2) Level Controls Hematopoietic Circulating Progenitor Cells Differentiation into Endothelial or Smooth Muscle Cells
title_short O(2) Level Controls Hematopoietic Circulating Progenitor Cells Differentiation into Endothelial or Smooth Muscle Cells
title_sort o(2) level controls hematopoietic circulating progenitor cells differentiation into endothelial or smooth muscle cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2678195/
https://www.ncbi.nlm.nih.gov/pubmed/19436758
http://dx.doi.org/10.1371/journal.pone.0005514
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