...
首页> 外文期刊>Tissue engineering >Time course of primary liver cell reorganization in three-dimensional high-density bioreactors for extracorporeal liver support: an immunohistochemical and ultrastructural study.
【24h】

Time course of primary liver cell reorganization in three-dimensional high-density bioreactors for extracorporeal liver support: an immunohistochemical and ultrastructural study.

机译:用于体外肝脏支持的三维高密度生物反应器中原代肝细胞重组的时间过程:免疫组织化学和超微结构研究。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

To enable extracorporeal liver support based on the use of primary liver cells, culture models supporting the maintenance of cell integrity and function in vitro are required. In this study the cell organization and ultrastructure of primary porcine hepatocytes cocultured with nonparenchymal cells in three-dimensional high-density bioreactors were analyzed after 10, 20, and 30 days of culture by immunohistochemistry and transmission electron microscopy. Biochemical data showed that metabolic activity of the cells in the system was relatively stable over at least 20 days. Immunohistochemical studies were performed in comparison with donor organ biopsies. They showed that hepatocytes and nonparenchymal cells reaggregated in bioreactors, forming structures partly resembling natural liver parenchyma. Bile duct-like structures characterized by cytokeratin 7 (CK-7) immunoreactivity (IR) were regularly detected. Nonparenchymal cells (vimentin IR) formed sinusoidal-like structures within parenchymal cell aggregates. Proliferative activity (Ki-67 IR) increased over time. The detection of collagen I and laminin indicated the production of extracellular matrix components within bioreactors. The results showed that primary liver cell reorganization and long-term maintenance of their differentiated state were achieved within the bioreactors The findings on cell proliferation indicated that the culture model is also of interest for further in vitro studies on cell regeneration and tissue formation.
机译:为了基于使用原代肝细胞获得体外肝支持,需要支持体外维持细胞完整性和功能的培养模型。在这项研究中,通过免疫组织化学和透射电镜分析了三维高密度生物反应器中与非实质细胞共培养的原代猪肝细胞的细胞组织和超微结构,分别在培养10、20和30天后进行了分析。生化数据表明,系统中细胞的代谢活性在至少20天内相对稳定。与供体器官活检相比,进行了免疫组织化学研究。他们显示,肝细胞和非实质细胞在生物反应器中重新聚集,形成部分类似于天然肝实质的结构。定期检测以细胞角蛋白7(CK-7)免疫反应性(IR)为特征的胆管样结构。非实质细胞(波形蛋白IR)在实质细胞聚集体内形成正弦样结构。增殖活性(Ki-67 IR)随时间增加。胶原蛋白I和层粘连蛋白的检测表明生物反应器内细胞外基质成分的产生。结果表明,在生物反应器中实现了原代肝细胞的重组和其分化状态的长期维持。细胞增殖的发现表明,该培养模型对于进一步的细胞再生和组织形成的体外研究也很有意义。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号