Akashi Makoto, Hayasaka Naoto, Yamazaki Shin, Node Koichi
Department of Vascular Failure Research, Faculty of Medicine, Saga University, Saga 849-8501, Japan.
J Neurosci. 2008 Apr 30;28(18):4619-23. doi: 10.1523/JNEUROSCI.3410-07.2008.
The suprachiasmatic nucleus (SCN) is the master circadian pacemaker driving behavioral and physiological rhythms in mammals. Circadian activation of mitogen-activated protein kinase [MAPK; also known as ERK (extracellular signal-regulated kinase)] is observed in vivo in the SCN under constant darkness, although the biological significance of this remains unclear. To elucidate this question, we first examined whether MAPK was autonomously activated in ex vivo SCN slices. Moreover, we investigated the effect of MAPK inhibition on circadian clock gene expression and neuronal firing rhythms using SCN-slice culture systems. We show herein that MAPK is autonomously activated in the SCN, and our data demonstrate that inhibition of the MAPK activity results in dampened rhythms and reduced basal levels in circadian clock gene expression at the SCN single-neuron level. Furthermore, MAPK inhibition attenuates autonomous circadian neuronal firing rhythms in the SCN. Thus, our data suggest that light-independent MAPK activity contributes to the robustness of the SCN autonomous circadian system.
视交叉上核(SCN)是驱动哺乳动物行为和生理节律的主昼夜节律起搏器。在持续黑暗条件下,体内SCN中可观察到丝裂原活化蛋白激酶[MAPK;也称为细胞外信号调节激酶(ERK)]的昼夜激活,但其生物学意义尚不清楚。为阐明这一问题,我们首先检测了离体SCN切片中MAPK是否自主激活。此外,我们使用SCN切片培养系统研究了MAPK抑制对昼夜节律时钟基因表达和神经元放电节律的影响。我们在此表明,MAPK在SCN中自主激活,我们的数据表明,在SCN单神经元水平上,抑制MAPK活性会导致节律减弱和昼夜节律时钟基因表达的基础水平降低。此外,MAPK抑制减弱了SCN中自主的昼夜神经元放电节律。因此,我们的数据表明,不依赖光的MAPK活性有助于SCN自主昼夜系统的稳健性。