Guissoni Campos Leila M, Hataka Alessandre, Vieira Isis Z, Buchaim Rogério L, Robalinho Isadora F, Arantes Giovanna E P S, Viégas Joyce S, Bosso Henrique, Bravos Rafael M, Pinato Luciana
São Paulo State University (UNESP), Marília, Brazil.
University of Marília (UNIMAR), Marília, Brazil.
Front Physiol. 2018 Feb 9;9:5. doi: 10.3389/fphys.2018.00005. eCollection 2018.
Oscillations of brain proteins in circadian rhythms are important for determining several cellular and physiological processes in anticipation of daily and seasonal environmental rhythms. In addition to the suprachiasmatic nucleus, the primary central oscillator, the cerebellum shows oscillations in gene and protein expression. The variety of local circuit rhythms that the cerebellar cortex contains influences functions such as motivational processes, regulation of feeding, food anticipation, language, and working memory. The molecular basis of the cerebellar oscillator has been demonstrated by "clock gene" expression within cells of the cerebellar layers. Genetic and epidemiological evidence suggests that disruption of circadian rhythms in humans can lead to many pathological conditions. Despite this importance, data about clock gene and protein expression in the cerebellum of diurnal (day-active) species, specifically primates, is currently poorly explored, mainly in regard to cellular identity, as well as the relationship with other molecules also involved in cerebellar functions. These studies could contribute to clarification of the possible mechanisms behind cerebellar rhythmicity. Considering that calcium binding proteins (CaBPs) play crucial roles in preserving and modulating cerebellar functions and that clock gene expression can be controlled by afferent projections or paracrine circadian signals such as the hormone melatonin, the present study aimed to describe cellular identities, distribution patterns and day/night expression changes in PER1, PER2, CaBPs, and MT and MT melatonin receptors in the cerebellar cortex of a diurnal primate using conventional fluorescence and peroxidase-antiperoxidase immunocytochemical techniques. PER1 and PER2 immunoreactive (IR) cells were observed in the Purkinje cells of the cerebellum, and MT and MT receptors were localized around Purkinje cells in the Pj layer in Bergmann cells. This identity was confirmed by the S100β-IR of these cells. The highest expression of PER seen in the daytime analysis coincided with the highest expression of melatonin receptors. CaBPs showed day/night morphological and density changes in the cerebellar cortex. The presence of the same temporal variations in the expression of PER in the Pj neurons and in MT and MT receptors in Bergmann cells indicates a possible relation between these cells during the rhythmic processing of the cerebellum, in addition to the CaBP temporal morphological and density changes.
大脑蛋白质的昼夜节律振荡对于预期每日和季节性环境节律来确定多种细胞和生理过程非常重要。除了主要的中央振荡器视交叉上核外,小脑也显示出基因和蛋白质表达的振荡。小脑皮质所包含的各种局部回路节律会影响动机过程、进食调节、食物预期、语言和工作记忆等功能。小脑振荡器的分子基础已通过小脑各层细胞内的“时钟基因”表达得到证实。遗传和流行病学证据表明,人类昼夜节律的破坏会导致许多病理状况。尽管具有这种重要性,但目前关于昼行性(白天活跃)物种,特别是灵长类动物小脑时钟基因和蛋白质表达的数据研究较少,主要涉及细胞特性以及与其他也参与小脑功能的分子的关系。这些研究可能有助于阐明小脑节律性背后的可能机制。考虑到钙结合蛋白(CaBPs)在维持和调节小脑功能中起关键作用,并且时钟基因表达可由传入投射或旁分泌昼夜信号如褪黑素激素控制,本研究旨在使用传统荧光和过氧化物酶 - 抗过氧化物酶免疫细胞化学技术描述昼行性灵长类动物小脑皮质中PER1、PER2、CaBPs以及MT和褪黑素MT受体的细胞特性、分布模式和昼夜表达变化。在小脑的浦肯野细胞中观察到PER1和PER2免疫反应性(IR)细胞,MT和MT受体位于伯格曼细胞中Pj层的浦肯野细胞周围。这些细胞的S100β - IR证实了这种特性。白天分析中观察到的PER最高表达与褪黑素受体的最高表达一致。CaBPs在小脑皮质中显示出昼夜形态和密度变化。Pj神经元中PER表达以及伯格曼细胞中MT和MT受体表达存在相同的时间变化,这表明除了CaBP的时间形态和密度变化外,这些细胞在小脑的节律性处理过程中可能存在关联。