Moore Helen A, Whitmore David
Centre for Cell and Molecular Dynamics, Department of Cell and Developmental Biology, University College London, London, United Kingdom.
PLoS One. 2014 Jan 22;9(1):e86176. doi: 10.1371/journal.pone.0086176. eCollection 2014.
Traditionally, circadian clocks have been thought of as a neurobiological phenomenon. This view changed somewhat over recent years with the discovery of peripheral tissue circadian oscillators. In mammals, however, the suprachiasmatic nucleus (SCN) in the hypothalamus still retains the critical role of a central synchronizer of biological timing. Zebrafish, in contrast, have always reflected a more highly decentralized level of clock organization, as individual cells and tissues contain directly light responsive circadian pacemakers. As a consequence, clock function in the zebrafish brain has remained largely unexplored, and the precise organization of rhythmic and light-sensitive neurons within the brain is unknown. To address this issue, we used the period3 (per3)-luciferase transgenic zebrafish to confirm that multiple brain regions contain endogenous circadian oscillators that are directly light responsive. In addition, in situ hybridization revealed localised neural expression of several rhythmic and light responsive clock genes, including per3, cryptochrome1a (cry1a) and per2. Adult brain nuclei showing significant clock gene expression include the teleost equivalent of the SCN, as well as numerous hypothalamic nuclei, the periventricular grey zone (PGZ) of the optic tectum, and granular cells of the rhombencephalon. To further investigate the light sensitive properties of neurons, expression of c-fos, a marker for neuronal activity, was examined. c-fos mRNA was upregulated in response to changing light conditions in different nuclei within the zebrafish brain. Furthermore, under constant dark (DD) conditions, c-fos shows a significant circadian oscillation. Taken together, these results show that there are numerous areas of the zebrafish central nervous system, which contain deep brain photoreceptors and directly light-entrainable circadian pacemakers. However, there are also multiple brain nuclei, which possess neither, demonstrating a degree of pacemaker complexity that was not previously appreciated.
传统上,昼夜节律钟一直被认为是一种神经生物学现象。近年来,随着外周组织昼夜节律振荡器的发现,这种观点有所改变。然而,在哺乳动物中,下丘脑的视交叉上核(SCN)仍然保留着作为生物节律中央同步器的关键作用。相比之下,斑马鱼一直反映出一种更为高度分散的生物钟组织水平,因为单个细胞和组织都含有直接对光作出反应的昼夜节律起搏器。因此,斑马鱼大脑中的生物钟功能在很大程度上仍未被探索,大脑中节律性和光敏感神经元的精确组织也尚不清楚。为了解决这个问题,我们使用了周期3(per3)-荧光素酶转基因斑马鱼来证实多个脑区含有直接对光作出反应的内源性昼夜节律振荡器。此外,原位杂交揭示了几种节律性和光反应性生物钟基因的局部神经表达,包括per3、隐花色素1a(cry1a)和per2。显示出显著生物钟基因表达的成体脑核包括硬骨鱼中相当于SCN的结构,以及众多下丘脑核、视顶盖的室周灰质区(PGZ)和后脑的颗粒细胞。为了进一步研究神经元的光敏感特性,我们检测了神经元活动标记物c-fos的表达。c-fos mRNA在斑马鱼大脑不同核中对光照条件变化作出反应时上调。此外,在持续黑暗(DD)条件下,c-fos表现出显著的昼夜节律振荡。综上所述,这些结果表明斑马鱼中枢神经系统中有许多区域含有深部脑光感受器和直接可被光调节的昼夜节律起搏器。然而,也有多个脑核既不含有光感受器也不含有昼夜节律起搏器,这表明了一种以前未被认识到的起搏器复杂性。