Itkes A V
Institute of Molecular Biology, Academy of Sciences of Russia, Moscow.
Prog Mol Subcell Biol. 1994;14:209-21. doi: 10.1007/978-3-642-78549-8_12.
The data obtained are in good agreement with the hypothesis that cAMP is involved in the control of 2-5A metabolism, including the mediation of the regulation of 2-5A by IFNs; 2-5A, in turn, affects the intracellular cAMP level. The general question originating from the data is that of a biochemical mechanism connecting the activation of the cAMP/2-5A system and the effect of depression of cell division. In my opinion, this universal effect is the result of the action of the known 2-5A-dependent mechanism, namely, RNase L (see review by Pestka et al. 1987), rather than by any new 2-5A-stimulating enzyme. The RNase L activated by 2-5A decreases the total level of protein synthesis and accelerates the degradation of cellular RNA, resulting in the inhibition of cell growth. It should be mentioned that such activation of RNA turnover is generally characteristic for nondividing cells, especially for cells in the resting state (Epifanova et al. 1983). Thus, the regulatory system of cAMP/2-5A is involved evidently in the antiproliferative mechanism characteristic for the resting cells, controlling the variations in the levels of RNA turnover and protein synthesis.
环磷酸腺苷(cAMP)参与了对2-5A代谢的调控,包括干扰素对2-5A调控的介导作用;反过来,2-5A又会影响细胞内cAMP水平。从这些数据中产生的一个普遍问题是,连接cAMP/2-5A系统激活与细胞分裂抑制效应的生化机制是什么。在我看来,这种普遍效应是已知的2-5A依赖性机制作用的结果,即核糖核酸酶L(见Pestka等人1987年的综述),而不是任何新的2-5A刺激酶。由2-5A激活的核糖核酸酶L会降低蛋白质合成的总体水平,并加速细胞RNA的降解,从而抑制细胞生长。应该提到的是,这种RNA周转的激活通常是非分裂细胞的特征,尤其是静止状态的细胞(Epifanova等人,1983年)。因此,cAMP/2-5A调节系统显然参与了静止细胞特有的抗增殖机制,控制着RNA周转水平和蛋白质合成的变化。