Yokota S, Yamamoto M, Moriya T, Akiyama M, Fukunaga K, Miyamoto E, Shibata S
Department of Pharmacology and Brain Science Waseda University, Tokorozawa, Saitama, Japan.
J Neurochem. 2001 Apr;77(2):618-27. doi: 10.1046/j.1471-4159.2001.00270.x.
It is known that Ca(2+)-dependent phosphorylation of cAMP response element binding protein (CREB) and the rapid induction of mPer1 and mPer2, mouse period genes in the suprachiasmatic nucleus (SCN) are associated with light-induced phase shifting. The CREB/CRE transcriptional pathway has been shown to be activated by calcium/calmodulin dependent kinase II (CaMKII) and mitogen-activated protein kinase (MAPK); however, there is a lack of evidence concerning whether the activation of CaMKII and/or MAPK elicited by photic stimuli are associated with the change in Per gene expression and behavioral phase shifting. In this experiment, we found there was an inhibitory effect by KN93, CaMKII inhibitor, on hamster Per1 and Per2 expression in the SCN and on phase delays in wheel running rhythm induced by light pulses. PD98059 and U0126, MAPK kinase inhibitors, however, affected neither light-induced Per1 and Per2 expression nor behavioral phase delays, even though PD98059 attenuated the light-induced phosphorylation of MAPK in the SCN. The present findings demonstrate that the light-induced activation of CaMKII plays an important role in the induction of Per1 and Per2 mRNA in the hamster SCN as well as phase shifting. These results suggest that gated induction of Per1 and/or Per2 genes through CaMKII-CREB/CRE accompanied with photic stimuli may be a critical step in phase shifting.
已知在视交叉上核(SCN)中,环磷酸腺苷反应元件结合蛋白(CREB)的钙依赖性磷酸化以及小鼠周期基因mPer1和mPer2的快速诱导与光诱导的相位移动有关。CREB/CRE转录途径已被证明可被钙/钙调蛋白依赖性激酶II(CaMKII)和丝裂原活化蛋白激酶(MAPK)激活;然而,关于光刺激引发的CaMKII和/或MAPK的激活是否与Per基因表达的变化和行为相位移动相关,缺乏证据。在本实验中,我们发现CaMKII抑制剂KN93对仓鼠SCN中Per1和Per2的表达以及光脉冲诱导的轮跑节律的相位延迟有抑制作用。然而,MAPK激酶抑制剂PD98059和U0126既不影响光诱导的Per1和Per2表达,也不影响行为相位延迟,尽管PD98059减弱了SCN中光诱导的MAPK磷酸化。目前的研究结果表明,光诱导的CaMKII激活在仓鼠SCN中Per1和Per2 mRNA的诱导以及相位移动中起重要作用。这些结果表明,通过CaMKII-CREB/CRE伴随光刺激对Per1和/或Per2基因进行门控诱导可能是相位移动的关键步骤。