Siegler E, Schaefer A, Bilello J A
Biosci Rep. 1982 Aug;2(8):605-8. doi: 10.1007/BF01314223.
The Friend murine erythroleukemia cell system and the Daudi Burkitt's lymphoma cell system were used to study the effect of growth-inhibitory concentrations of interferon on membrane functions. Experiments with Friend-cell clones sensitive and resistant to interferon indicated that a number of changes in membrane transport occur rapidly after the addition of interferon to sensitive cells. While no change was observed in the activity of the (Na+/K+) ATPase in Friend cells sensitive or resistant to interferon, a piretanide-inhibitable Na+,K+, 2Cl- co-transport system was specifically inhibited after interferon treatment of sensitive cells. In contrast, treatment of Daudi cells with purified molecularly cloned or standard preparations of human leukocyte interferon gave rise to no early changes in the transport of amino acids, 32Pi, sugars, or 86Rb+. The major change observed in Daudi cells was a marked reduction in the uptake and incorporation of thymidine, which begins to decrease after 8-10 h of exposure to interferon.
利用Friend小鼠红白血病细胞系统和Daudi伯基特淋巴瘤细胞系统研究了生长抑制浓度的干扰素对膜功能的影响。对干扰素敏感和耐药的Friend细胞克隆实验表明,向敏感细胞中添加干扰素后,膜转运迅速发生了许多变化。虽然在对干扰素敏感或耐药的Friend细胞中,未观察到(Na+/K+)ATP酶活性的变化,但在用干扰素处理敏感细胞后,吡咯他尼可抑制的Na+、K+、2Cl-共转运系统受到了特异性抑制。相比之下,用纯化的分子克隆或标准制剂的人白细胞干扰素处理Daudi细胞,氨基酸、32Pi、糖类或86Rb+的转运没有早期变化。在Daudi细胞中观察到的主要变化是胸腺嘧啶核苷摄取和掺入的显著减少,在暴露于干扰素8 - 10小时后开始下降。