2007Journal of Tongji UniversityRequires access

The cultivation of the human umbilical vein endothelial cell in vitro

Feng Bo

Open publisher page 1 citations

Abstract

Objective To explore the culture method of the human umbilical vein endothelial cell(HUVEC) in vitro.Methods HUVECs were acquired with type I collagenase treatment and cultivated in RPMI-1640 containing 20% FBS;the passage was developed with 0.25% trypsinase and 0.02% EDTA.The ECs were identified under the light microscope with immunohistochemical method.Results The primary cells began to attach and grow after being inoculated 4 hours,and grew to monolayer 5-7 days later.They presented cobblestone-appearance with contact inhibition under the light microscope,and the antigens of human Ⅷ factor were positive according to immunohistochemical method.Conclusion Collagenase typeⅠ perfusion is an effective way to cultivate the human umbilical vein endothelial cells in vitro.

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What this paper is about

Objective To explore the culture method of the human umbilical vein endothelial cell(HUVEC) in vitro.Methods HUVECs were acquired with type I collagenase treatment and cultivated in RPMI-1640 containing 20% FBS;the passage was developed with 0.25% trypsinase and 0.02% EDTA.The ECs were identified under the light microscope with immunohistochemical method.Results The primary cells began to attach and grow after being inoculated 4 hours,and grew to monolayer 5-7 days later.They presented cobblestone-appearance with contact inhibition under the light microscope,and the antigens of human Ⅷ factor were positive according to immunohistochemical method.Conclusion Collagenase typeⅠ perfusion is an effective way to cultivate the human umbilical vein endothelial cells in vitro.

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Available abstract

Objective To explore the culture method of the human umbilical vein endothelial cell(HUVEC) in vitro.Methods HUVECs were acquired with type I collagenase treatment and cultivated in RPMI-1640 containing 20% FBS;the passage was developed with 0.25% trypsinase and 0.02% EDTA.The ECs were identified under the light microscope with immunohistochemical method.Results The primary cells began to attach and grow after being inoculated 4 hours,and grew to monolayer 5-7 days later.They presented cobblestone-appearance with contact inhibition under the light microscope,and the antigens of human Ⅷ factor were positive according to immunohistochemical method.Conclusion Collagenase typeⅠ perfusion is an effective way to cultivate the human umbilical vein endothelial cells in vitro.

Key concepts: Umbilical vein, Collagenase, In vitro, Human umbilical vein endothelial cell, Immunohistochemistry, Vein, Endothelial stem cell, Andrology

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