Albert D, Kowalski J, Nodzenski E, Micek M, Wu P
Department of Medicine, University of Chicago Medical Center, IL 60637.
Biochem Biophys Res Commun. 1990 Mar 16;167(2):383-90. doi: 10.1016/0006-291x(90)92033-v.
Cyclic adenosine monophosphate arrests proliferating T lymphocytes in the G1 phase of the cell cycle. Here we demonstrate that exogenous and endogenous elevations in cyclic AMP concentration result in diminished mitogen stimulation, cell cycle arrest, and decreased ribonucleotide reductase messenger RNA concentrations in peripheral blood mononuclear cells. At lower concentrations (less than 1mM) of dibutyryl cyclic AMP that do not generate cell cycle arrest there is inhibition of ribonucleotide reductase activity without decreased messenger RNA concentration for the M2 subunit of ribonucleotide reductase. However, at higher concentrations of dibutyryl cyclic AMP there is G1 cell cycle arrest and reduced M2 specific messenger RNA concentration. Thus, cyclic AMP inhibition of lymphocyte activation may occur by different mechanisms that are dose dependent.
环磷酸腺苷使增殖的T淋巴细胞停滞于细胞周期的G1期。在此我们证明,外源性和内源性环磷酸腺苷浓度升高会导致外周血单核细胞中丝裂原刺激减弱、细胞周期停滞以及核糖核苷酸还原酶信使核糖核酸浓度降低。在不会导致细胞周期停滞的较低浓度(小于1mM)的二丁酰环磷酸腺苷作用下,核糖核苷酸还原酶活性受到抑制,而核糖核苷酸还原酶M2亚基的信使核糖核酸浓度并未降低。然而,在较高浓度的二丁酰环磷酸腺苷作用下,会出现G1期细胞周期停滞且M2特异性信使核糖核酸浓度降低。因此,环磷酸腺苷对淋巴细胞激活的抑制作用可能通过不同的剂量依赖性机制发生。