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在Biosilon微载体上大规模生产和培养肝细胞。

Large-scale production and cultivation of hepatocytes on Biosilon microcarriers.

作者信息

Shnyra A, Bocharov A, Bochkova N, Spirov V

机构信息

Department of Cellular Biology, Academy of Medical Sciences, Moscow, U.S.S.R.

出版信息

Artif Organs. 1990 Dec;14(6):421-8. doi: 10.1111/j.1525-1594.1990.tb02998.x.

Abstract

A method for large-scale production of hepatocytes on microcarriers have been developed for the purpose of bioartificial liver support system. Hepatocytes obtained by collagenase treatment of rat liver were efficiently attached and spread on a microcarrier surface in the presence of O2-saturated perfluorodecalin. In order to compare the metabolic activities of hepatocytes under long-term cultivation on microcarriers with those of cells under conventional monolayer culture, some liver-specific functions were investigated. Microcarrier-attached hepatocytes cultured in the absence of serum for 8 days synthesized and secreted albumin and fibronectin. Moreover, hepatocytes on microcarriers retained the ability to conjugate bilirubin for 4-5 days. With respect to these specific metabolic properties, microcarrier-attached hepatocytes were comparable to those from routine dish culture. These results suggest that this method developed for large-scale production of hepatocytes on microcarriers will allow one to obtain metabolically active cells suitable for extracorporeal liver support systems.

摘要

为了生物人工肝支持系统的目的,已开发出一种在微载体上大规模生产肝细胞的方法。通过胶原酶处理大鼠肝脏获得的肝细胞,在充满氧气的全氟萘烷存在下,能有效地附着并铺展在微载体表面。为了比较微载体上长期培养的肝细胞与传统单层培养细胞的代谢活性,对一些肝脏特异性功能进行了研究。在无血清条件下在微载体上培养8天的附着于微载体的肝细胞合成并分泌白蛋白和纤连蛋白。此外,微载体上的肝细胞保持结合胆红素的能力达4 - 5天。就这些特定的代谢特性而言,附着于微载体的肝细胞与常规培养皿培养的肝细胞相当。这些结果表明,这种在微载体上大规模生产肝细胞的方法将使人们能够获得适合体外肝支持系统的具有代谢活性的细胞。

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