Published online before print September 27, 2004, doi: 10.1161/01.CIR.0000143161.01901.BD
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(Circulation. 2004;110:2039-2046.)
© 2004 American Heart Association, Inc.
Vascular Medicine |
Cytokine-Induced Mobilization of Circulating Endothelial Progenitor Cells Enhances Repair of Injured Arteries
From the Department of Medicine (D.K., L.G.M., M.G., L.Z., C.C.L., R.E.P., V.J.D.), Brigham and Women’s Hospital and Harvard Medical School, Boston, Mass; the Department of Physiology (L.G.M.), Queen’s University, Kingston, Ontario, Canada; and the Department of Genetics (G.M.), Children’s Hospital, Boston, Mass. Dr Kong is currently at the School of Life Science, Nankai University, Tianjin, China.
Correspondence to Victor J. Dzau, MD, Office of the Chancellor, Duke University Medical Center, DUMC 3701, Durham, NC 27710. E-mail victor.dzau{at}duke.edu
Received October 21, 2003; de novo received February 28, 2004; revision received May 17, 2004; accepted May 20, 2004.
Background— The existence of circulating endothelial progenitor cells (CEPCs) has previously been documented. These cells can be mobilized by cytokines and are recruited to sites of injury, where they may participate in tissue repair. In the present study, we examined the hypothesis that mobilization of CEPCs by exogenous granulocyte-colony stimulating factor (G-CSF) enhances repair of injured arteries by facilitating reendothelialization and inhibiting neointima development.
Methods and Results— Male rats were injected daily with 50 µg/kg recombinant human G-CSF or 0.9% NaCl SC for 8 days. On the fifth day of treatment, 1 mL of blood was collected for fluorescence-activated cell sorting analysis of mononuclear cells, and the animals underwent balloon angioplasty of the common carotid artery. The animals were killed at 2 or 4 weeks after injury, and the carotid arteries were harvested and processed for immunohistochemistry, scanning electron microscopy (SEM), and morphometric analysis of endothelialization and neointimal formation. G-CSF increased the number of circulating mononuclear cells that express endothelial cell lineage markers several-fold. SEM and immunohistochemical staining with the endothelial marker, platelet and endothelial cell adhesion molecule-1, showed rapid and nearly complete (>90%) reendothelialization of the denuded vessels in the G-CSF–treated animals compared with <20% in the control animals. Reendothelialization was paralleled by a decrease in inflammation in the vessel wall. Neointima thickness was reduced by 
60% in the G-CSF–treated animals compared with control animals at 2 and 4 weeks after injury.
Conclusion— We postulate that cytokine-induced mobilization of CEPCs may be a suitable therapeutic strategy for prevention of restenosis after revascularization procedures.
Key Words: growth substances • restenosis • endothelium • immunohistochemistry
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