Ungemach F R, Hegner D
Arch Toxicol. 1980 Mar;44(1-3):167-73. doi: 10.1007/BF00303193.
Thymidine transport and phosphorylation were investigated in isolated rat hepatocytes and AS 30 D hepatoma cells. In contrast to hepatoma cells, hepatocytes exhibited a minimum of thymidine phosphorylation due to a 100-fold smaller thymidine kinase activity. In hepatocytes thymidine is transported by two transport systems: a specific concentrative "high affinity" system and an unspecific non-concentrative "low affinity" system. In hepatoma cells only the "low affinity" system could be detected. A single dose of 20 or 50 mg diethylnitrosamine/kg body weight induced in hepatocytes a remakable increas of thymidine kinase activity and a decrease of the transport by the "high affinity" system. Thymidine transport and phosphorylation by hepatocytes are considered to be sensitive markers for early recognition of toxin-induced liver regeneration.
在分离的大鼠肝细胞和AS 30 D肝癌细胞中研究了胸苷的转运和磷酸化。与肝癌细胞相比,肝细胞由于胸苷激酶活性小100倍而表现出最低限度的胸苷磷酸化。在肝细胞中,胸苷通过两种转运系统转运:一种特异性浓缩的“高亲和力”系统和一种非特异性非浓缩的“低亲和力”系统。在肝癌细胞中,只能检测到“低亲和力”系统。单次剂量20或50mg/kg体重的二乙基亚硝胺可诱导肝细胞中胸苷激酶活性显著增加,并使“高亲和力”系统的转运减少。肝细胞的胸苷转运和磷酸化被认为是早期识别毒素诱导的肝脏再生的敏感标志物。