Tsuchiya Yoshiki, Minami Itsunari, Kadotani Hiroshi, Nishida Eisuke
Department of Cell and Developmental Biology, Graduate School of Biostudies, Kyoto University, Sakyo-ku, Kyoto, Japan.
EMBO Rep. 2005 Mar;6(3):256-61. doi: 10.1038/sj.embor.7400356.
In mammals, the master circadian pacemaker is located in the suprachiasmatic nucleus (SCN) of the hypothalamus. The SCN is thought to drive peripheral oscillators by controlling neuronal and humoral signals that can entrain the peripheral clocks. Here, we show that prostaglandin E2 (PGE2), a proinflammatory compound known to have diverse biological effects, is able to act as an in vivo clock-resetting agent. We find that in cultured NIH3T3 fibroblasts, PGE2 is able to induce transient expression of Period 1 messenger RNA and the following circadian oscillation of clock gene expression. Furthermore, we demonstrate that intraperitoneal administration of PGE2 results in the phase shift of circadian gene expression in mouse peripheral tissues in a time-dependent manner. This phase shift is also induced by the EP1/EP3 agonist sulprostone but not by the EP2 agonist butaprost. The PGE2-induced phase shift is inhibited by the EP1 antagonist SC-51322. These results suggest that PGE2 acts as an in vivo clock-resetting factor by means of the EP1 subtype of PGE receptors.
在哺乳动物中,主昼夜节律起搏器位于下丘脑的视交叉上核(SCN)。人们认为SCN通过控制能够使外周生物钟同步的神经和体液信号来驱动外周振荡器。在此,我们表明前列腺素E2(PGE2),一种已知具有多种生物学效应的促炎化合物,能够作为一种体内生物钟重置剂。我们发现,在培养的NIH3T3成纤维细胞中,PGE2能够诱导周期蛋白1信使核糖核酸的瞬时表达以及随后生物钟基因表达的昼夜振荡。此外,我们证明腹腔注射PGE2会导致小鼠外周组织中昼夜节律基因表达以时间依赖性方式发生相位偏移。这种相位偏移也可由EP1/EP3激动剂舒前列素诱导,但不能由EP2激动剂布他前列素诱导。PGE2诱导的相位偏移被EP1拮抗剂SC - 51322抑制。这些结果表明,PGE2通过PGE受体的EP1亚型作为一种体内生物钟重置因子发挥作用。