| ObjectiveTo observe the expression of CXCL12from the EPCs transfected byAdv-HIF-1αmuand investigate the effect to the EPCs.MethodsUnion inducting and culturing the MNCs separated by density gradientcentrifugation combined with VEGFã€EGF and bFGF into EPCs and identifyingits angiogenic activity; Adv-HIF-1αmu transfected into EPCs by the optimummultiplicity of infection (MOI),and the EPCs containing the purpose gene asgroup A obtained. The EPCs transfected merely Adv as group B.The EPCs nottransfected Adv-HIF-1αmu as group C.The expression of HIF-1in transfectedEPCs were determined by Western Blot, the concentration of supernatant byELSA and the migration of exogenous EPCs by transwell.Results1ã€The MNCs obtained by density gradient centrifugation can be inducedand cultured into EPCs by EGFã€bFGF and VEGF,which can combine withUEA-1and uptake ac-LDL and are angiogenic;2ã€Group A (i.e. the transfection Adv-HIF-1αmu) of EPCs can expressHIF-1, and group B (not transfection Adv-HIF-1αmu EPCs) and group C (puretransfection Adv the EPCs) no expression of HIF–1ï¼›3〠ELISA showed that expression of CXCL12is up-ragulated intransfected EPCs compared with other two groups, there is no obvious differences between group A and Bï¼›4ã€The supernatant fluid of EPCs after transfection can promote themigration of exogenous EPCs, the migration quantity of cells in group A ishigher than in group B and group C (P>0.05), no obvious difference wasfound between group B and group C (P <0.05)ConclusionsThe MNCs obtained by density gradient centrifugation can be induced andcultured into the characteristic EPCs within EGFã€bFGF and VEGF,and theEPCs transfected by Adv-HIF-1αmucan express highly HIF-1and CXCL12,and induce the migration of exogenous EPCs. |