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视交叉上核中光诱导的细胞外信号调节激酶激活的时间调控

Temporal regulation of light-induced extracellular signal-regulated kinase activation in the suprachiasmatic nucleus.

作者信息

Butcher Greg Q, Lee Boyoung, Obrietan Karl

机构信息

Department of Neuroscience, The Ohio State University, Columbus, Ohio 43210, USA.

出版信息

J Neurophysiol. 2003 Dec;90(6):3854-63. doi: 10.1152/jn.00524.2003. Epub 2003 Aug 20.

Abstract

Signaling via the p42/p44 mitogen activated protein kinase (MAPK) pathway has been implicated as an intermediate event coupling light to entrainment of the mammalian circadian clock located in the suprachiasmatic nucleus (SCN). To examine how photic input dynamically regulates the activation state of the MAPK pathway, we monitored extracellular signal-regulated kinase (ERK) activation using different light stimulus paradigms. Compared with control animals not exposed to light, a 15 min light exposure during the early night triggered a marked increase in ERK activation and the translocation of ERK from the cytosol to the nucleus. ERK activation peaked 15 min after light onset, then returned to near basal levels within approximately 45 min. The MAPK pathway could be reactivated multiple times by light pulses spaced 45 min apart, indicating that the MAPK cascade rapidly resets and resolves individual light pulses into discrete signaling events. Under conditions of constant light (120 min), the time course for ERK activation, nuclear translocation, and inactivation was similar to the time course observed after a 15-min light treatment. The parallels between the ERK inactivation profiles elicited by a 15 and a 120 min light exposure suggest that SCN cells contain a MAPK pathway signal-termination mechanism that limits the duration of pathway activation. This concept was supported by the observation that the small G protein Ras, a regulator of the MAPK pathway, remained in the active, GTP-bound, state under conditions of constant light (120-min duration), indicating that photic information was relayed to the SCN and that SCN cells maintained their responsiveness for the duration of the light treatment. The SCN expressed both nuclear MAPK phosphatases (MKP-1 and MKP-2) and the cytosolic MAPK phosphatase Mkp-3, thus providing mechanisms by which light-induced ERK activation is terminated. Collectively, these observations provide important new information regarding the regulation of the MAPK cascade, a signaling intermediate that couples light to resetting of the SCN clock.

摘要

通过p42/p44丝裂原活化蛋白激酶(MAPK)途径的信号传导被认为是将光与位于视交叉上核(SCN)的哺乳动物生物钟的同步化联系起来的一个中间事件。为了研究光输入如何动态调节MAPK途径的激活状态,我们使用不同的光刺激模式监测细胞外信号调节激酶(ERK)的激活情况。与未暴露于光的对照动物相比,在深夜进行15分钟的光照会引发ERK激活的显著增加以及ERK从细胞质向细胞核的转位。ERK激活在光照开始后15分钟达到峰值,然后在大约45分钟内恢复到接近基础水平。MAPK途径可以被间隔45分钟的光脉冲多次重新激活,这表明MAPK级联反应能够迅速重置并将单个光脉冲解析为离散的信号事件。在持续光照(120分钟)的条件下,ERK激活、核转位和失活的时间进程与15分钟光照处理后观察到的时间进程相似。15分钟和120分钟光照引发的ERK失活曲线之间的相似性表明,SCN细胞含有一种MAPK途径信号终止机制,该机制限制了途径激活的持续时间。这一概念得到了以下观察结果的支持:小G蛋白Ras是MAPK途径的调节因子,在持续光照(120分钟)条件下仍保持活性的、结合GTP的状态,这表明光信息被传递到了SCN,并且SCN细胞在光照处理期间保持了它们的反应性。SCN表达了核MAPK磷酸酶(MKP-1和MKP-2)以及细胞质MAPK磷酸酶Mkp-3,从而提供了终止光诱导的ERK激活的机制。总的来说,这些观察结果提供了关于MAPK级联反应调节的重要新信息,MAPK级联反应是一种将光与SCN生物钟重置联系起来的信号中间体。

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