Basic & Clinical Medicine ›› 2008, Vol. 28 ›› Issue (5): 428-431.
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Fei-lan CHEN, Hua-rong ZHANG, Cheng-ping XU, Xiu-wu BIAN
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Abstract: objective To explore the effect of chemokine SDF-1 on the proliferation, migration and in vitro of human endothelial progenitor cells (EPCs). Methods The expression of CXCR4 and SDF-1 on EPCs was detected with immunocytochemistry. Proliferation, migration and in vitro tubulogenesis of EPCs were detected by MTT, Millicell chemotaxis and three-diamensional in vitro Matrigel assays, respectively. When activation or inactivation of SDF-1/CXCR4 axis with CXCR4 ligand SDF-1 or CXCR4 inhibitor AMD3100. Results SDF-1 and CXCR4 were expressed on EPCs. SDF-1 induced proliferation, migration and tubulogenesis of EPCs. However, AMD3100 abolished the effects induced by SDF-1. Conclusion The SDF-1/CXCR4 axis possibly plays a critical role in regulating vasculogenesis of EPCs
Key words: EPCs, CXCR4, neovascularization
Fei-lan CHEN; Hua-rong ZHANG; Cheng-ping XU; Xiu-wu BIAN. Activation of SDF-1/CXCR4 Axis Induces Proliferation, Migration, and Tubulogenesis of Human Endothelial Progenitor Cells[J]. Basic & Clinical Medicine, 2008, 28(5): 428-431.
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URL: http://journal11.magtechjournal.com/Jwk_jcyxylc/EN/
http://journal11.magtechjournal.com/Jwk_jcyxylc/EN/Y2008/V28/I5/428