O2 Level Controls Hematopoietic Circulating Progenitor Cells Differentiation into Endothelial or Smooth Muscle Cells

被引:27
作者
Berthelemy, Nicolas
Kerdjoudj, Halima
Schaaf, Pierre
Prin-Mathieu, Christine
Lacolley, Patrick
Stoltz, Jean-Francois
Voegel, Jean-Claude
Menu, Patrick
机构
[1] Group of Bioengineering (UMR CNRS 7561), UHP-Nancy 1, Faculté de Médecine, Vandoeuvre-lès-Nancy
[2] Institut Charles Sadron (UPR 22, CNRS), Strasbourg
[3] CHU Nancy and UHP-Nancy 1, Faculté de Médecine, Vandoeuvre-lès-Nancy
[4] Institut National de la Santé et de la Recherche Médicale, (INSERM Unité 961), UHP-Nancy 1, Faculté de Médecine, Vandoeuvre-lès-Nancy
[5] Institut National de la Santé et de la Recherche Médicale, (INSERM Unité 977), Université de Strasbourg, Faculté de chirurgie dentaire, Strasbourg
来源
PLOS ONE | 2009年 / 4卷 / 05期
关键词
ENGINEERED BLOOD-VESSELS; HUMAN UMBILICAL ARTERIES; PERIPHERAL-BLOOD; HYPOXIA; TRANSPLANTATION; EXPRESSION; CLONING; GRAFTS; GROWTH; MODEL;
D O I
10.1371/journal.pone.0005514
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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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页数:9
相关论文
共 38 条
[1]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[2]   Isoform switching from SM-B to SM-A myosin results in decreased contractility and altered expression of thin filament regulatory proteins [J].
Babu, GJ ;
Pyne, GJ ;
Zhou, YB ;
Okwuchukuasanya, C ;
Brayden, JE ;
Osol, G ;
Paul, RJ ;
Low, RB ;
Periasamy, M .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 287 (03) :C723-C729
[3]   Engineering of muscle tissue [J].
Bach, AD ;
Stern-Straeter, J ;
Beier, JP ;
Bannasch, H ;
Stark, GB .
CLINICS IN PLASTIC SURGERY, 2003, 30 (04) :589-+
[4]   Polyelectrolyte films boost progenitor cell differentiation into endothelium-like monolayers [J].
Berthelemy, Nicolas ;
Kerdjoudj, Halima ;
Gaucher, Caroline ;
Schaaf, Pierre ;
Stolz, Jean-Francois ;
Lacolley, Patrick ;
Voegel, Jean-Claude ;
Menu, Patrick .
ADVANCED MATERIALS, 2008, 20 (14) :2674-+
[5]  
BISSELL MJ, 1987, J CELL SCI, P327
[6]   Time-dependent modulation of alignment and differentiation of smooth muscle cells seeded on a porous substrate undergoing cyclic mechanical strain [J].
Cha, JM ;
Park, TN ;
Noh, TH ;
Suh, T .
ARTIFICIAL ORGANS, 2006, 30 (04) :250-258
[7]   The evaluation of a small-diameter polysaccharide-based arterial graft in rats [J].
Chaouat, Marc ;
Le Visage, Catherine ;
Autissier, Aude ;
Chaubet, Frederic ;
Letourneur, Didier .
BIOMATERIALS, 2006, 27 (32) :5546-5553
[8]   Molecular mechanisms of blood vessel growth [J].
Conway, EM ;
Collen, D ;
Carmeliet, P .
CARDIOVASCULAR RESEARCH, 2001, 49 (03) :507-521
[9]   Expression of VEGF isoforms by epiphyseal chondrocytes during low-oxygen tension is HIF-1α dependent [J].
Cramer, T ;
Schipani, E ;
Johnson, RS ;
Swoboda, B ;
Pfander, D .
OSTEOARTHRITIS AND CARTILAGE, 2004, 12 (06) :433-439
[10]   Hypoxia-induced pulmonary artery adventitial remodeling and neovascularization: contribution of progenitor cells [J].
Davie, NJ ;
Crossno, JT ;
Frid, MG ;
Hofmeister, SE ;
Reeves, JT ;
Hyde, DM ;
Carpenter, TC ;
Brunetti, JA ;
McNiece, IK ;
Stenmark, KR .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2004, 286 (04) :L668-L678