Cayanis E, Russo J J, Wu Y S, Edelman I S
Center for Reproductive Sciences, College of Physicians and Surgeons, Columbia University, New York, New York 10032.
J Membr Biol. 1992 Jan;125(2):163-70. doi: 10.1007/BF00233355.
Cultured ARL15 cells respond to abnormally low extracellular K+ concentrations by increasing the abundance of Na,K-ATPase (the Na/K pump). This response is preceded by significant increases in the mRNAs of the alpha 1 and beta 1 subunits of this enzyme, implying transcriptional or post-transcriptional regulation in the response. The present study concerned the possible participation of serum factors in low K+ induction of Na,K-ATPase. In normal K+ (4.5 mM) or low K+ (0.68 mM) the presence of 10% calf serum had no effect on Na,K-ATPase activity. The serum independence of the response to low K+ raised the possibility that low K+ may itself elicit a "growth" response. Accordingly, the effect of low K+ on mRNA abundances of four proto-oncogenes (c-fos, c-myc, c-jun and c-ski) was evaluated in the early phase of the response by quantitative Northern blot analysis. The mRNA for c-fos was transiently elevated by low K+, with a peak at 30 min. In contrast, low K+ had no measurable effect on the abundances of c-myc, c-jun and c-ski, for up to 2 hr of exposure. The early elevation of c-fos mRNA makes it a candidate mediator in this signal-transduction pathway. Induction of c-fos mRNA by the phorbol ester, PMA, or by dioctanoyl glycerol, however, had no effect on Na,K-ATPase activity. These results indicate that an increase in c-fos mRNA alone is not sufficient to induce Na,K-ATPase. Whether induction of c-fos is necessary for the response to low K+ remains to be determined in future studies.
培养的ARL15细胞通过增加钠钾ATP酶(钠钾泵)的丰度来响应异常低的细胞外钾离子浓度。在这种反应之前,该酶的α1和β1亚基的mRNA会显著增加,这意味着在该反应中存在转录或转录后调控。本研究关注血清因子在低钾诱导钠钾ATP酶过程中的可能参与情况。在正常钾离子浓度(4.5 mM)或低钾离子浓度(0.68 mM)下,10%小牛血清的存在对钠钾ATP酶活性没有影响。对低钾反应的血清非依赖性增加了低钾本身可能引发“生长”反应的可能性。因此,通过定量Northern印迹分析在反应的早期阶段评估了低钾对四种原癌基因(c-fos、c-myc、c-jun和c-ski)mRNA丰度的影响。低钾使c-fos的mRNA短暂升高,在30分钟时达到峰值。相比之下,在长达2小时的暴露时间内,低钾对c-myc、c-jun和c-ski的丰度没有可测量的影响。c-fos mRNA的早期升高使其成为该信号转导途径中的候选介质。然而,佛波酯PMA或二辛酰甘油诱导c-fos mRNA对钠钾ATP酶活性没有影响。这些结果表明,仅c-fos mRNA的增加不足以诱导钠钾ATP酶。c-fos的诱导对于低钾反应是否必要仍有待未来研究确定。