2006Journal of Shihezi UniversityRequires access

Primary Culture Method of Endothelial Cells Derived from Human Umbilical Vein

Huimin Zhang

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Abstract

To establish a method of culturing primary cells derived from human umbilical vein,endothelial cells of human umbilical vein were digested with collagenase Ⅱ,cultured in DMEM medium with 10% FBS,with or withnot EGF(epidermal growth factor),followed by immunocytochemical technique to verify HUVEC.The HUVEC grow the fastest in 3~4 days,in a pattern of contact inhibition,showing a cobblestone or pitching stone-like appearance.It was proved that high purity EC can be harvested with digestion of collagenase Ⅱperfusion with high survival rate.This method provides experimental model for vascular EC research.

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What this paper is about

To establish a method of culturing primary cells derived from human umbilical vein,endothelial cells of human umbilical vein were digested with collagenase Ⅱ,cultured in DMEM medium with 10% FBS,with or withnot EGF(epidermal growth factor),followed by immunocytochemical technique to verify HUVEC.The HUVEC grow the fastest in 3~4 days,in a pattern of contact inhibition,showing a cobblestone or pitching stone-like appearance.It was proved that high purity EC can be harvested with digestion of collagenase Ⅱperfusion with high survival rate.This method provides experimental model for vascular EC research.

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Available abstract

To establish a method of culturing primary cells derived from human umbilical vein,endothelial cells of human umbilical vein were digested with collagenase Ⅱ,cultured in DMEM medium with 10% FBS,with or withnot EGF(epidermal growth factor),followed by immunocytochemical technique to verify HUVEC.The HUVEC grow the fastest in 3~4 days,in a pattern of contact inhibition,showing a cobblestone or pitching stone-like appearance.It was proved that high purity EC can be harvested with digestion of collagenase Ⅱperfusion with high survival rate.This method provides experimental model for vascular EC research.

Key concepts: Umbilical vein, Collagenase, Primary culture, Andrology, Vein, Chemistry, Digestion (alchemy), Perfusion

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