...
首页> 外文期刊>World Journal of Gastroenterology >Primary hepatocyte culture in collagen gel mixture and collagen sandwich
【24h】

Primary hepatocyte culture in collagen gel mixture and collagen sandwich

机译:胶原凝胶混合物和胶原三明治中的原代肝细胞培养

获取原文
获取原文并翻译 | 示例
           

摘要

AIM: To explore the methods of hepatocytes culture in a collagen gel mixture or between double layers of collagen sandwich configuration and to examine the functional and cytomorphological characteristics of cultured hepatocytes. METHODS: A two-step collagenase perfusion technique was used to isolate the hepatocytes from Wistar rats or newborn Chinese experimental piglets. The isolated hepatocytes were cultured in a collagen gel mixture or between double layers of collagen sandwich configuration respectively. The former was that rat hepatocytes were mixed with type Ⅰ rat tail collagen solution till gelled, and the medium was added onto the gel. The latter was that swine hepatocytes were seeded on a plate precoated with collagen gel for 24 h, then another layer of collagen gel was overlaid, resulting in a sandwich configuration. The cytomorphological characteristics, albumin secretion, and LDH-release of the hepatocytes cultured in these two models were examined. RESULTS: Freshly isolated rat hepatocytes were successfully mixed and fixed in collagen gel, and cultured in the gel condition. During the culture period, the urea synthesized and secreted by rat hepatocytes was detected throughout the period. Likewise, newborn experimental piglet hepatocytes were successfully fixed between the double layers of collagen gel, forming a sandwich configuration. Within a week of culture, the albumin secreted by swine hepatocytes was detected by SDS/PAGE analysis. The typical cytomorphological characteristics of the hepatocytes cultured by the above two culture models were found under a phase-contrast microscope. There was little LDH-release during the culture period. CONCLUSION: Both collagen gel mixture and double layers of collagen sandwich configuration can provide cultural conditions much closer to in vivo environment, and are helpful for maintaining specific hepatic functions and cytomorphological characteristics. A collagen gel mixture culture may be more eligible for the study of bioartificial livers.
机译:目的:探讨在胶原蛋白凝胶混合物中或双层胶原蛋白夹心结构之间培养肝细胞的方法,并检查培养的肝细胞的功能和细胞形态学特征。方法:采用两步胶原酶灌注技术从Wistar大鼠或新生的中国实验仔猪中分离肝细胞。分离的肝细胞分别在胶原蛋白凝胶混合物中或在胶原蛋白夹心结构的双层之间培养。前者是将大鼠肝细胞与Ⅰ型大鼠尾部胶原溶液混合直至凝胶化,然后将培养基加入凝胶中。后者是将猪肝细胞接种在预先涂有胶原蛋白凝胶的板上24小时,然后覆盖另一层胶原蛋白凝胶,形成三明治结构。检查了在这两个模型中培养的肝细胞的细胞形态学特征,白蛋白分泌和LDH释放。结果:新鲜分离的大鼠肝细胞成功混合并固定在胶原凝胶中,并在凝胶条件下培养。在培养期间,在整个过程中检测到大鼠肝细胞合成和分泌的尿素。同样,新生的实验仔猪肝细胞被成功地固定在胶原凝胶的双层之间,形成了三明治结构。在培养的一周内,通过SDS / PAGE分析检测了猪肝细胞分泌的白蛋白。在相差显微镜下发现了以上两种培养模型培养的肝细胞的典型细胞形态学特征。在培养期间几乎没有LDH释放。结论:胶原蛋白凝胶混合物和双层胶原蛋白三明治结构均可提供更接近体内环境的培养条件,并有助于维持特定的肝功能和细胞形态学特征。胶原蛋白凝胶混合物培养物可能更适合于生物人工肝的研究。

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