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Isolation and characterization of vascular endothelial cells derived from fetal tooth buds of miniature swine

机译:小型猪胎牙芽来源的血管内皮细胞的分离与鉴定

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摘要

The aim of the present study was to isolate endothelial cells from tooth buds (unerupted deciduous teeth) of miniature swine. Mandibular molar tooth buds harvested from swine fetuses at fetal days 90–110 were cultured in growth medium supplemented with 15% fetal bovine serum in 100-mm culture dishes until the primary cells outgrown from the tooth buds reached confluence. A morphologically defined set of pavement-shaped primary cells were picked up manually with filter paper containing trypsin/ethylenediamine tetraacetic acid solution and transferred to a separate dish. A characterization of the cellular characteristics and a functional analysis of the cultured cells at passages 3 to 5 were performed using immunofluorescence, a reverse transcriptase polymerase chain reaction assay, a tube formation assay, and transmission electron microscopy. The isolated cells grew in a pavement arrangement and showed the characteristics of contact inhibition upon reaching confluence. The population doubling time was ~48 h at passage 3. As shown by immunocytostaining and western blotting with specific antibodies, the cells produced the endothelial marker proteins such as vascular endothelial cadherin, von Willebrand factor, and vascular endothelial growth factor receptor-2. Observation with time-lapse images showed that small groups of cells aggregated and adhered to each other to form tube-like structures. Moreover, as revealed through transmission electron microscopy, these adherent cells had formed junctional complexes. These endothelial cells from the tooth buds of miniature swine are available as cell lines for studies on tube formation and use in regenerative medical science.
机译:本研究的目的是从小型猪的牙芽(未脱落的乳齿)中分离出内皮细胞。在100-mm培养皿中,在胎龄90-110天从猪胎儿收获的下颌磨牙牙芽在添加了15%胎牛血清的生长培养基中培养,直到从牙芽长出的原代细胞汇合为止。用含有胰蛋白酶/乙二胺四乙酸溶液的滤纸手动拾取一组形态学确定的路面形原代细胞,并转移到另一个培养皿中。使用免疫荧光,逆转录酶聚合酶链反应测定,管形成测定和透射电子显微镜对第3-5代的细胞特征进行表征和对培养的细胞进行功能分析。分离的细胞以人行道排列生长,并在达到汇合时显示出接触抑制的特征。传代3时,种群倍增时间约为48小时。如通过免疫细胞染色和特异抗体的Western印迹显示,细胞产生了内皮标记蛋白,例如血管内皮钙黏着蛋白,von Willebrand因子和血管内皮生长因子受体2。随时间推移的图像观察表明,一小组细胞聚集并相互粘附,形成管状结构。此外,如通过透射电子显微镜所揭示的,这些贴壁细胞已形成连接复合物。这些来自小型猪牙芽的内皮细胞可作为细胞系用于研究管的形成,并用于再生医学。

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  • 作者单位

    Research Center for Odontology School of Life Dentistry at Tokyo The Nippon Dental University">(1);

    Department of Developmental and Regenerative Dentistry School of Life Dentistry at Tokyo The Nippon Dental University">(2);

    Department of Developmental and Regenerative Dentistry School of Life Dentistry at Tokyo The Nippon Dental University">(2);

    Department of Developmental and Regenerative Dentistry School of Life Dentistry at Tokyo The Nippon Dental University">(2);

    Department of Developmental and Regenerative Dentistry School of Life Dentistry at Tokyo The Nippon Dental University">(2);

    Research Center for Odontology School of Life Dentistry at Tokyo The Nippon Dental University">(1);

    Department of Anatomy The Jikei University School of Medicine">(3);

    Department of NDU Life Sciences School of Life Dentistry at Tokyo The Nippon Dental University">(4);

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Sus scrofa; Miniature pig; Tooth buds; Endothelial cells; Tube formation;

    机译:Sus scrofa;小型猪牙芽;内皮细胞管形成;

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