JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES)

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QIN Hongwei1,2, XIAO Dongjie1, LIU Jie3, HU An-la1, MA Xiao-li1, WANG Yun-shan1, ZHANG Hong-wei4   

  1. 1. Center of Medical Laboratory Diagnosis, Jinan Central Hospital, Clinical Medical College of Shandong University,Jinan 250013, Shandong, China; 2. Department of Biology, Jining Teachers′ College, Qufu 273155,Shandong, China
  • Received:2006-09-29 Revised:1900-01-01 Online:2006-12-24 Published:2006-12-24
  • Contact: QIN Hong-wei

Abstract: To establish the method of isolation of endothelial progenitor cells(EPCs)from human peripheral blood and identify the markers of EPCs by FACS to provide basis for angiogenesis therapy. Methods: Total mononuclear cells (MNC) were isolated from peripheral blood by Ficoll density gradient centrifugation, Results:Adherent cells doublepositive for DilACLDL and FITCUEA1 could be observed under fluorescent and confocal laser microscope at 4 days after culture.KDR was (2.50±1.47)%,(5.72±1.66)% and (36.24±3.24)%, respectively at day 4 of culture. At days 5, 6 and 7, CD34+ cells were (8.45±3.97)%, (14.13±2.79)% and (21.14±2.91)% and CD31+ cells were (22.52±3.86)%, (42.76±3.67)% and (54.67±3.44)%, respectively. Conclusion:EPCs exist in the peripheral blood and can be differentiated into mature endothelial cells(ECs). FACS can be used to efficiently identify EPCs for angiogenesis study.

Key words: Endothelial progenitor cells, Cell culture, Surface markers

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