Honzlová Petra, Semenovykh Kateryna, Sumová Alena
Laboratory of Biological Rhythms, Institute of Physiology, The Czech Academy of Sciences, Videnska 1083, Prague, Czech Republic.
Faculty of Science, Charles University, Prague, Czech Republic.
Cell Mol Neurobiol. 2023 Apr;43(3):1319-1333. doi: 10.1007/s10571-022-01252-1. Epub 2022 Jul 11.
The activity of the immune system is controlled by circadian clocks present in different immune cells. The brain-resident subtype of immune cells, microglia, exhibits a wide range of functional phenotypes depending on the signaling molecules in their microenvironment. The exact role of microglia in the hypothalamic suprachiasmatic nuclei (SCN), the central circadian clock, has not been known. Therefore, the aim of this study was to determine (1) whether microenvironment-induced changes in microglial polarization affect circadian clocks in these cells and (2) whether the presence of microglia contributes to SCN clock function. Microglial and SCN clocks were monitored using PER2-driven bioluminescence rhythms at the tissue and single-cell levels. We found that polarization of resting microglia to a pro-inflammatory (M1) or anti-inflammatory (M2) state significantly altered the period and amplitude of their molecular circadian clock; importantly, the parameters changed plastically with the repolarization of microglia. This effect was reflected in specific modulations of the expression profiles of individual clock genes in the polarized microglia. Depletion of microglia significantly reduced the amplitude of the SCN clock, and co-cultivation of the SCN explants with M2-polarized microglia specifically improved the amplitude of the SCN clock. These results demonstrate that the presence of M2-polarized microglia has beneficial effects on SCN clock function. Our results provide new insight into the mutual interaction between immune and circadian systems in the brain.
免疫系统的活动由存在于不同免疫细胞中的昼夜节律时钟控制。免疫细胞的脑驻留亚型——小胶质细胞,根据其微环境中的信号分子表现出广泛的功能表型。小胶质细胞在下丘脑视交叉上核(SCN)(即中央昼夜节律时钟)中的确切作用尚不清楚。因此,本研究的目的是确定:(1)小胶质细胞极化的微环境诱导变化是否会影响这些细胞中的昼夜节律时钟;(2)小胶质细胞的存在是否有助于SCN时钟功能。在组织和单细胞水平上,使用PER2驱动的生物发光节律监测小胶质细胞和SCN时钟。我们发现,静息小胶质细胞向促炎(M1)或抗炎(M2)状态的极化显著改变了其分子昼夜节律时钟的周期和振幅;重要的是,这些参数随着小胶质细胞的重新极化而发生可塑性变化。这种效应反映在极化小胶质细胞中各个时钟基因表达谱的特定调节上。小胶质细胞的缺失显著降低了SCN时钟的振幅,而SCN外植体与M2极化小胶质细胞的共培养特异性地提高了SCN时钟的振幅。这些结果表明,M2极化小胶质细胞的存在对SCN时钟功能具有有益作用。我们的结果为大脑中免疫和昼夜节律系统之间的相互作用提供了新的见解。