Dapergola Eleni, Menegazzi Pamela, Raabe Thomas, Hovhanyan Anna
Institute of Medical Radiation and Cell Research, Biozentrum, University of Würzburg, Würzburg, Germany.
Neurobiology and Genetics, Theodor-Boveri Institute, Biozentrum, University of Würzburg, Würzburg, Germany.
Front Cell Dev Biol. 2021 Mar 5;9:595754. doi: 10.3389/fcell.2021.595754. eCollection 2021.
Endogenous clocks enable organisms to adapt cellular processes, physiology, and behavior to daily variation in environmental conditions. Metabolic processes in cyanobacteria to humans are under the influence of the circadian clock, and dysregulation of the circadian clock causes metabolic disorders. In mouse and , the circadian clock influences translation of factors involved in ribosome biogenesis and synchronizes protein synthesis. Notably, nutrition signals are mediated by the insulin receptor/target of rapamycin (InR/TOR) pathways to regulate cellular metabolism and growth. However, the role of the circadian clock in brain development and the potential impact of clock impairment on neural circuit formation and function is less understood. Here we demonstrate that changes in light stimuli or disruption of the molecular circadian clock cause a defect in neural stem cell growth and proliferation. Moreover, we show that disturbed cell growth and proliferation are accompanied by reduced nucleolar size indicative of impaired ribosomal biogenesis. Further, we define that light and clock independently affect the InR/TOR growth regulatory pathway due to the effect on regulators of protein biosynthesis. Altogether, these data suggest that alterations in InR/TOR signaling induced by changes in light conditions or disruption of the molecular clock have an impact on growth and proliferation properties of neural stem cells in the developing brain.
内源性生物钟使生物体能够根据环境条件的日常变化来调整细胞过程、生理机能和行为。从蓝细菌到人类,代谢过程都受到昼夜节律钟的影响,而昼夜节律钟失调会导致代谢紊乱。在小鼠中,昼夜节律钟影响核糖体生物合成相关因子的翻译,并使蛋白质合成同步。值得注意的是,营养信号由胰岛素受体/雷帕霉素靶蛋白(InR/TOR)途径介导,以调节细胞代谢和生长。然而,昼夜节律钟在大脑发育中的作用以及生物钟功能受损对神经回路形成和功能的潜在影响尚不清楚。在此,我们证明光刺激的变化或分子生物钟的破坏会导致神经干细胞生长和增殖出现缺陷。此外,我们表明细胞生长和增殖受到干扰时,核仁大小会减小,这表明核糖体生物合成受损。进一步地,我们明确由于对蛋白质生物合成调节因子的影响,光和生物钟独立影响InR/TOR生长调节途径。总之,这些数据表明,光照条件变化或分子生物钟破坏所诱导的InR/TOR信号改变,会影响发育中大脑神经干细胞的生长和增殖特性。