Hauschka P V, Everhart L P, Rubin R W
Proc Natl Acad Sci U S A. 1972 Dec;69(12):3542-6. doi: 10.1073/pnas.69.12.3542.
Cultured Chinese hamster ovary cells showed no significant change in generation time or fraction in the S-phase in the presence of 1 mM N(6),O(2')-dibutyryl adenosine 3':5'-cyclic monophosphate. Growth continued for at least two generations after expression of the morphological transformation induced by this cyclic AMP analog. Despite identical growth rates, apparent rates of DNA and RNA synthesis (incorporation of [(3)H]-thymidine or [(3)H]uridine) were reduced up to 15-fold in log phase by 1 mM cyclic nucleotide. [(3)H]Deoxycytidine incorporation was much less sensitive to dibutyryl cyclic AMP. Uptake studies with [(3)H]thymidine demonstrated an inhibition of transport rate dependent on the concentration of dibutyryl cyclic AMP in the growth medium. The rate of thymidine uptake at 1 degrees was decreased 21-fold by 1 mM cyclic nucleotide; half-maximal inhibition occurred at 6 muM. At 37 degrees , the pool size of acid-soluble thymidylate was strongly reduced by 1 mM cyclic nucleotide, and synergistic reduction of the pool size was found with 0.5 mM aminophylline. Phosphorylation of the acid-soluble intracellular label was unaffected by dibutyryl cyclic AMP. Inhibition of thymidine uptake is attributed to an observed decrease in thymidine kinase activity caused by growth in 1 mM dibutyryl cyclic AMP, and possibly to a simultaneous alteration in membrane permeability. Kinase-facilitated uptake of other metabolites may be regulated in a similar fashion by cyclic AMP.
在存在1 mM N(6),O(2')-二丁酰腺苷3':5'-环磷酸单酯的情况下,培养的中国仓鼠卵巢细胞在世代时间或S期比例方面没有显著变化。在这种环磷酸腺苷类似物诱导的形态转化表达后,生长持续了至少两代。尽管生长速率相同,但在对数期,1 mM环核苷酸可使DNA和RNA合成的表观速率([3H] - 胸苷或[3H] - 尿苷的掺入)降低多达15倍。[3H] - 脱氧胞苷掺入对二丁酰环磷酸腺苷的敏感性要低得多。用[3H] - 胸苷进行的摄取研究表明,转运速率的抑制取决于生长培养基中二丁酰环磷酸腺苷的浓度。1 mM环核苷酸可使1℃时胸苷摄取速率降低21倍;半最大抑制浓度为6 μM。在37℃时,1 mM环核苷酸可使酸溶性胸苷酸的库大小显著降低,并且发现0.5 mM氨茶碱可协同降低库大小。酸溶性细胞内标记物的磷酸化不受二丁酰环磷酸腺苷的影响。胸苷摄取的抑制归因于在1 mM二丁酰环磷酸腺苷中生长导致的胸苷激酶活性的观察到的降低,并且可能还归因于膜通透性的同时改变。环磷酸腺苷可能以类似的方式调节激酶促进的其他代谢物的摄取。