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Tissue culture of human and canine thoracic duct endothelium.

作者信息

Gnepp D R, Chandler W

出版信息

In Vitro Cell Dev Biol. 1985 Apr;21(4):200-6. doi: 10.1007/BF02620930.

DOI:10.1007/BF02620930
PMID:2409072
Abstract

Endothelial cells from the canine or human thoracic duct were harvested using 0.2% collagenase digestion and grown in Media 199 supplemented with fetal bovine serum. The canine endothelial cells grew to confluence (4.4 to 12 X 10(4) cells/cm2) in 6 to 10 d; doubling times ranged from 1.5 to 2.8 d. There was a minimum critical density for cell growth between 5000 and 10 000 cells/cm2. The canine endothelial cells have been maintained in culture for periods up to 11 mo. The human thoracic duct endothelial cells are more difficult to grow and maintain. Endothelial cells were isolated from 5 out of 35 human thoracic ducts and grew for periods of up to 2 wk before degenerating. Both human and canine endothelial cells were Factor VIII positive. It has thus been demonstrated that it is possible to grow canine and, less easily, human thoracic duct endothelium in tissue culture.

摘要

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本文引用的文献

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Technique for cloning bovine aortic endothelial cells.牛主动脉内皮细胞克隆技术。
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Expression of Ia-like antigens by human vascular endothelial cells is inducible in vitro: demonstration by monoclonal antibody binding and immunoprecipitation.人血管内皮细胞Ia样抗原的表达在体外可被诱导:通过单克隆抗体结合和免疫沉淀证明。
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处于血管生成和淋巴管生成交叉点的淋巴管
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Electron microscopy of cell surfaces of Paramecium caudatum stained with ruthenium red.用钌红染色的尾草履虫细胞表面的电子显微镜观察。
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Long-term culture of capillary endothelial cells.毛细血管内皮细胞的长期培养。
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