Chinese Journal of Tissue Engineering Research

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Biological characteristics of endothelial progenitor cells from the peripheral blood versus umbilical cord blood

Wu Hong-tao1, Ma Yan2, Bi Xiao-juan2, Jiang Ming2, Yang Kai1, Wang Ning1   

  1. 1Department of No.1 Cadre Ward Medicine, First Affiliated Hospital, Xinjiang Medical University, Urumqi  830000, Xinjiang Uygur Autonomous Region, China; 2Stem Cell Laboratory, Medical Research Center, First Affiliated Hospital, Xinjiang Medical University, Urumqi  830000, Xinjiang Uygur Autonomous Region, China
  • Revised:2013-09-02 Online:2013-11-05 Published:2013-11-05
  • Contact: Wang Ning, M.D., Chief physician, Master’s supervisor, Department of No.1 Cadre Ward Medicine, First Affiliated Hospital, Xinjiang Medical University, Urumqi 830000, Xinjiang Uygur Autonomous Region, China 13999994126@163.com
  • About author:Wu Hong-tao★, Studying for master’s degree, Department of No.1 Cadre Ward Medicine, First Affiliated Hospital, Xinjiang Medical University, Urumqi 830000, Xinjiang Uygur Autonomous Region, China whtbmd_2008@126.com
  • Supported by:

    the Natural Science Foundation of Xinjiang Uygur Autonomous Region, No. 2011211A075*

Abstract:

BACKGROUND: Endothelial progenitor cells from the peripheral blood and umbilical cord blood are an essential source to repair vascular endothelial cells damaged by various diseases.
OBJECTIVE: To compare the biological characteristics of endothelial progenitor cells from peripheral blood and umbilical cord blood in vitro.
METHODS: Mononuclear cells were isolated from the umbilical cord blood and peripheral blood with density gradient centrifugation method and 6% hydroxyethyl starch precipitation combined with density gradient centrifugation method, respectively. Mononuclear cells were counted. Then the cells were implanted on the culture plate pre-paved with rat tail collagen at the concentration of 1×106/cm2, and cultured in an endothelial cell culture medium for 7 days.
RESULTS AND CONCLUSION: Isolated and cultured endothelial progenitor cells from the peripheral blood and umbilical cord blood had similar morphological characteristics in vitro. Under the optical microscope, with the increase of culturing days, most adherent cells were changed from round to spindle-shaped. Peripheral blood endothelial progenitor cells had cell colony formation, and spindle cells from the umbilical cord blood arranged typically in a line structure. After trypan blue staining and drawing of cell growth curves, the number of mononuclear cells and endothelial progenitor cells, survival rate and proliferative ability of endothelial progenitor cells from the peripheral blood were all lower than those from the umbilical cord blood (P < 0.05). At day 3 after incubation, the proliferation of endothelial progenitor cells from the peripheral blood and umbilical cord blood reached the peak, and then showed a decreased tendency. Flow cytometry and Immunofluorescence staining showed that endothelial progenitor cells from the peripheral blood and umbilical cord blood could express CD34, CD133, and vascular endothelial cell factor receptor 2. The endothelial progenitor cells from the peripheral blood and umbilical cord blood could swallow acetylated low density lipoprotein and be combined with ulex europaeus agglutinin Ⅰ. The results confirmed that the endothelial progenitor cells from the peripheral blood and cord blood have similar biologicla characteristics, but the proliferation ability of endothelial progenitor cells from the cord blood is higher.

Key words: stem cells, endothelium, umbilical cord, centrifugation, tissue engineering

CLC Number: