Tolón R, Franco F S, Villuendas G, Vicente A B, Palacios N, Cacicedo L
Endocrine Services, Hospital Ramón y Cajal and Hospital Carlos III, Carretera de Colmenar Km 9, 28034, Madrid, Spain.
Brain Res. 2000 Jun 23;868(2):338-46. doi: 10.1016/s0006-8993(00)02352-0.
In the nervous system, signals transmitted across synapses are known to regulate gene expression in the postsynaptic cells. This process often involves membrane depolarization and subsequent elevation of intracellular Ca(2+). We have previously demonstrated in fetal cerebrocortical cells, that somatostatin (SS) mRNA levels can be induced by depolarizing agents such as high potassium concentrations and veratridine (VTD), and that these effects are calcium dependent. SS expression is regulated by cAMP, and in the cerebral cortex adenylate cyclase activity is regulated through fluctuations in intracellular Ca(2+) concentrations. The present experiments were undertaken to determine the mechanism by which calcium upregulates the levels of SS mRNA. Cerebrocortical cells from 17-day-old fetuses were exposed to the different agents for 24 h and the levels of SS mRNA were measured by Northern blot. Incubation of cells with the calcium channel antagonist nifedipine (Nf), the calcium chelating agent EGTA, calcium free KRB and the calcium calmodulin inhibitors trifluoroperazine (TFP) and the napthelene sulfonamide, W7, resulted in the inhibition of K(+)-induced SS mRNA levels. K(+)-evoked depolarization increased the intracellular concentration of cAMP and this effect was antagonized by verapamil (VPM). Forskolin (Fk) provoked a higher increment in cAMP concentration than potassium, although the induction of SS mRNA was more evident following K(+) depolarization indicating a lack of correlation between levels of cAMP and induction of SS mRNA. The role of K(+)-induced cAMP on the increment of SS mRNA that occurred upon membrane depolarization was further explored with the inhibitor of protein kinase A (PKA), Rp cAMP whose presence significantly reduced depolarization-induced SS mRNA levels. This study confirms that Ca(2+) influx is required for K(+)depolarization-induced stimulation of cAMP whereby the increment of SS mRNA is partly produced.
在神经系统中,已知跨突触传递的信号可调节突触后细胞中的基因表达。这一过程通常涉及膜去极化以及随后细胞内Ca(2+)浓度的升高。我们之前在胎儿脑皮质细胞中已证明,生长抑素(SS)mRNA水平可被去极化剂如高钾浓度和藜芦碱(VTD)诱导,且这些效应依赖于钙。SS的表达受cAMP调节,在大脑皮质中,腺苷酸环化酶活性通过细胞内Ca(2+)浓度的波动来调节。本实验旨在确定钙上调SS mRNA水平的机制。将17日龄胎儿的脑皮质细胞暴露于不同试剂24小时,并用Northern印迹法测量SS mRNA水平。用钙通道拮抗剂硝苯地平(Nf)、钙螯合剂乙二醇双乙醚二胺四乙酸(EGTA)、无钙的Krebs-Ringer缓冲液(KRB)以及钙调蛋白抑制剂三氟拉嗪(TFP)和萘磺酰胺W7孵育细胞,导致K(+)诱导的SS mRNA水平受到抑制。K(+)诱发的去极化增加了细胞内cAMP浓度,而这种效应被维拉帕米(VPM)拮抗。福斯可林(Fk)引起的cAMP浓度升高比钾更高,尽管K(+)去极化后SS mRNA的诱导更明显,这表明cAMP水平与SS mRNA的诱导之间缺乏相关性。用蛋白激酶A(PKA)抑制剂Rp cAMP进一步探究了K(+)诱导的cAMP对膜去极化时发生的SS mRNA增加的作用,其存在显著降低了去极化诱导的SS mRNA水平。本研究证实,Ca(2+)内流是K(+)去极化诱导cAMP刺激所必需的,由此部分产生了SS mRNA的增加。