Kwok C S, Chapman I V
Int J Radiat Biol Relat Stud Phys Chem Med. 1977 Nov;32(5):409-29. doi: 10.1080/09553007714551171.
A TdR carrier-transport system, believed to be facilitated diffusion, has been shown to exist in Ehrlich ascites tumour cells. It is suggested that this system is the predominant transport mechanism at low extracellular concentrations (less than 1-5 micron). The transport system was damaged considerably by 5 krad X-radiation, resulting in a 30-35 per cent reduction in the initial total TdR uptake rat at low extracellular concentrations and 15-20 min after irradiation. The extent of the damage was dependent on the age of the cells as was reflected by relative decreases in V max and Km. It can be concluded that the enhanced depression in 14C-TdR incorporation into DNA of irradiated cells when low precursor concentrations were used for monitoring, is partly attributed to the radiation-induced damage to the carrier-transport system. The permeability constant for passive diffusion in asynchronous E.A.T. cells and the endogenous natural rate of dTTP synthesis in S-phase cells were estimated.
一种胸苷(TdR)载体转运系统,据信为易化扩散,已证实在艾氏腹水瘤细胞中存在。有人提出,该系统是细胞外低浓度(小于1 - 5微米)时的主要转运机制。该转运系统受到5千拉德X射线辐射的严重损伤,导致在细胞外低浓度以及照射后15 - 20分钟时,初始总胸苷摄取率降低30 - 35%。损伤程度取决于细胞的年龄,这通过最大反应速度(V max)和米氏常数(Km)的相对降低得以体现。可以得出结论,当使用低前体浓度监测时,照射细胞中14C - TdR掺入DNA的增强抑制,部分归因于辐射对载体转运系统的损伤。估算了异步生长的艾氏腹水瘤细胞中被动扩散的渗透常数以及S期细胞中dTTP合成的内源性自然速率。