Vereninov A A, Marakhova I I, Osipov V V, Toropova F V
Institute of Cytology, Academy of Sciences, St. Petersburg, Russian Federation.
FEBS Lett. 1993 Jan 18;316(1):37-40. doi: 10.1016/0014-5793(93)81732-f.
Increase in Na+, K(+)-ATPase mRNAs was detected in activated lymphocytes by the RT-PCR method. alpha 1 subunit mRNA gradually increased with time and by 36 h was 2.4 times higher than at the start. Increase in the beta 1 mRNA was transient reaching a maximum in the 8 h probe and declining to the initial level in the 24 and 36 h probes. The elevation of Na+, K(+)-ATPase mRNAs does not underlie a cycloheximide-inhibited increase in cation pumping peculiar to the prereplicative period as can be judged from the fact that Act D fails to eliminate PHA-induced enhancement of pump fluxes.
采用逆转录聚合酶链反应(RT-PCR)方法检测到活化淋巴细胞中Na⁺,K⁺-ATP酶mRNA有所增加。α1亚基mRNA随时间逐渐增加,至36小时时比开始时高2.4倍。β1 mRNA的增加是短暂的,在8小时探针时达到最大值,在24小时和36小时探针时降至初始水平。从放线菌素D未能消除PHA诱导的泵通量增强这一事实可以判断,Na⁺,K⁺-ATP酶mRNA的升高并非复制前期特有的阳离子泵受放线菌酮抑制的增加的基础。