Laishes B A, Williams G M
In Vitro. 1976 Jul;12(7):521-32. doi: 10.1007/BF02796495.
The conditions for obtaining representative, primary adult rat hepatocyte cultures were explored. The methods applied included enzymatic liver perfusion which was nondestructive to hepatocytes, the prevention of aggregation of dissociated cells and the selective attachment of viable cells. These procedures yielded a recovery of 50% of the liver cells which gave rise to cultures representing 14% of the total liver cells. The cultures were composed of homogeneous epithelial-like cells cytologically similar to hepatocytes and possessed a number of liver-specific enzymes. There was virtually no cell division initially and most cells died between 24 and 48 hr. Insulin enhanced the attachment of the liver cells, altered their morphology, but did not prolong cell survival.
探索了获得具有代表性的原代成年大鼠肝细胞培养物的条件。所采用的方法包括对肝细胞无损的酶促肝脏灌注、防止解离细胞聚集以及活细胞的选择性附着。这些操作回收了50%的肝细胞,这些肝细胞形成的培养物占肝脏细胞总数的14%。培养物由细胞学上与肝细胞相似的均匀上皮样细胞组成,并具有多种肝脏特异性酶。最初几乎没有细胞分裂,大多数细胞在24至48小时之间死亡。胰岛素增强了肝细胞的附着,改变了它们的形态,但没有延长细胞存活时间。