Watts P, Smith M D, Edwards I, Zammit V, Brown V, Grant H
Bioengineering Unit, University of Strathclyde, Wolfson Centre, Glasgow, UK.
J Hepatol. 1995 Nov;23(5):605-12. doi: 10.1016/0168-8278(95)80069-7.
Rat and sheep primary hepatocytes have been cultured in four different medium formulations: Williams' E, Chee's, Medium 199 and Modified Earle's. The total cytochrome P450 content, intracellular concentration of reduced glutathione, rate of urea synthesis and total protein content of cultures of cells from both species in each medium have been determined. Modified Earle's and Chee's medium proved to be the most favourable formulations for the culture of rat hepatocytes. After 48 h, cells cultured in Modified Earle's had significantly more cytochrome P450 and a significantly greater rate of urea synthesis than cells in any other medium. After 6 days in culture the difference in cytochrome P450 levels between rat hepatocytes in Chee's medium and those in Modified Earle's medium was abrogated. The difference in the rate of urea synthesis between rat hepatocytes cultured in each of these two media was shown to be more dependent on the medium in which the cells were maintained during the period of urea synthesis measurement than on the medium in which the cells had been previously cultured. Sheep hepatocytes cultured in Chee's medium ruptured and died within 24 h. Apart from this, sheep cells were less sensitive to changes in medium formulation than were rat hepatocytes. The initial plating efficiency was lower in sheep cells. Total cytochrome P450 content was the most discriminatory of the four parameters for evaluating the status of rat hepatocyte cultures. However, urea synthesis may be the most useful parameter for assessment of hepatocyte function in hybrid liver devices such as bioartificial liver support systems where access to the cells during operation of the device is restricted.
威廉姆斯E培养基、池氏培养基、199培养基和改良伊格尔培养基。已测定了每种培养基中这两种细胞培养物的总细胞色素P450含量、细胞内还原型谷胱甘肽浓度、尿素合成速率和总蛋白含量。改良伊格尔培养基和池氏培养基被证明是培养大鼠肝细胞最适宜的配方。48小时后,在改良伊格尔培养基中培养的细胞比在其他任何培养基中的细胞具有显著更多的细胞色素P450和显著更高的尿素合成速率。培养6天后,池氏培养基中的大鼠肝细胞与改良伊格尔培养基中的大鼠肝细胞在细胞色素P450水平上的差异消失。结果表明,在这两种培养基中培养的大鼠肝细胞之间尿素合成速率的差异,更多地取决于在尿素合成测量期间细胞所维持的培养基,而不是细胞先前培养所用的培养基。在池氏培养基中培养的绵羊肝细胞在24小时内破裂并死亡。除此之外,绵羊细胞对培养基配方变化的敏感性低于大鼠肝细胞。绵羊细胞的初始接种效率较低。总细胞色素P450含量是评估大鼠肝细胞培养状态的四个参数中最具区分性的。然而,对于评估混合肝装置(如生物人工肝支持系统)中的肝细胞功能而言,尿素合成可能是最有用的参数,因为在该装置运行期间获取细胞受到限制。