Vascular Biology |
From INSERM E-0016, Faculté de Médecine Paris V, Université René Descartes, Paris, France.
Correspondence to Julie Sainz, INSERM E-0016, Faculté de Médecine Paris V, Necker-Enfants Malades, 156, Rue de Vaugirard, 75015 Paris, France. E-mail sainz{at}necker.fr
Objective Circulating progenitors and stem cells have been reported to contribute to angiogenesis and arterial repair after injury. In the present study, we investigated whether the arterial wall could host permanently residing progenitor cells under physiological context.
Methods and Results Using the Hoechst-based flow cytometry method, we identified and isolated progenitor cells termed side population (SP) cells at a prevalence of 6.0±0.8% in the tunica media of adult mice aortas. Arterial SP cells expressed the ATP-binding cassette transporter subfamily G member 2, frequently present on SP cell surface, and displayed a Sca-1+ c-kit/low Lin CD34/low profile. They did not form myeloid or lymphoid hematopoietic colonies after plating in methylcellulose-based medium. Importantly, cultured SP cells were able to acquire the phenotype of endothelial cells (CD31, VE-cadherin, and von Willebrand factor expression) or of smooth muscle cells (
-smooth muscle actin, calponin, and smooth muscle myosin heavy chain expression), in presence of either vascular endothelial growth factor or transforming growth factor (TGF)-ß1/PDGF-BB, respectively. Moreover, they generated vascular-like branching structures, composed of both VE-cadherin+ cells and
-smooth muscle actin+ cells on Matrigel.
Conclusions In this study, we provide the first evidence to our knowledge that in the adult mice, the normal arterial wall harbors SP cells with vascular progenitor properties.
Key Words: endothelial cells smooth muscle cells SP cells vascular progenitors vasculogenesis
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