Zhang Min, Ma Zhuoyao, Cui Haoran, Miao Yumeng, Yin Yu, Wen Qing, Liu Zhihui, Huang Xin, Xing Chen, Liu Kun, Peng Hui, Song Lun
Beijing Institute of Basic Medical Sciences, Beijing, China.
College of Life Science, Henan Normal University, Xinxiang, China.
Sci Rep. 2025 Apr 10;15(1):12253. doi: 10.1038/s41598-025-96931-6.
Lack of sleep is a common problem in current society, which can induce various brain dysfunctions. Neuroinflammation is a typical reaction caused by sleep deficit and is considered as a common basis for various neurological disorders and cognitive impairments, but the related mechanisms have not been fully clarified. The circadian clock protein plays a critical role in maintaining physiological homeostasis, including sleep/wake cycles. Circadian disorders induced by sleep deficit might contribute to the development of neuroinflammation. In the current study, we observed that sleep deprivation (SD) induced elevated expression of High-mobility group box 1 (HMGB1), one of the most important mediators of neuroinflammation, in the cortical microglia and cerebrospinal fluids. Moreover, acetylation-dependent nuclear export of HMGB1 was involved in up-regulation and secretion of HMGB1 after sleep deprivation. Further studies indicated that sleep deprivation induced an increase in the expression of acetyltransferase p300 and a decrease in the expression of deacetylase SIRT1, which synergistically enhanced the acetylation level of HMGB1 in the cortical microglial cells, thereby triggered the nuclear export and secretion of HMGB1. Most importantly, circadian clock protein PER2 constitutively interacted with p300 and inhibited its expression in the microglial cells, which can be interrupted by PER2 downregulation upon sleep deprivation, leading to the increased expression of p300 and acetylation and secretion of HMGB1. The truncated PER2 mutant without p300 binding ability lost its ability to regulate p300 expression, indicating that PER2 functioned as a co-suppressor of p300 in regulating acetylation and expression of HMGB1. Taken together, data in this study reveal a new mechanism by which PER2 is involved in controlling HMGB1 dependent neuroinflammation induced by sleep deprivation. Maintaining PER2 levels or blocking HMGB1 acetylation in the cortex might be prospective for preventing sleep deprivation-induced neuroinflammation and the related adverse reactions in the brain.
睡眠不足是当今社会的一个常见问题,它会引发各种大脑功能障碍。神经炎症是睡眠不足引起的一种典型反应,被认为是各种神经疾病和认知障碍的共同基础,但相关机制尚未完全阐明。生物钟蛋白在维持生理稳态(包括睡眠/觉醒周期)中起着关键作用。睡眠不足引起的生物钟紊乱可能会促进神经炎症的发展。在本研究中,我们观察到睡眠剥夺(SD)会导致皮质小胶质细胞和脑脊液中神经炎症最重要的介质之一——高迁移率族蛋白B1(HMGB1)的表达升高。此外,HMGB1的乙酰化依赖性核输出参与了睡眠剥夺后HMGB1的上调和分泌。进一步研究表明,睡眠剥夺会导致乙酰转移酶p300表达增加,去乙酰化酶SIRT1表达减少,二者协同增强了皮质小胶质细胞中HMGB1的乙酰化水平,从而触发HMGB1的核输出和分泌。最重要的是,生物钟蛋白PER2与p300持续相互作用并抑制其在小胶质细胞中的表达,睡眠剥夺会使PER2下调,从而中断这种相互作用,导致p300表达增加以及HMGB1的乙酰化和分泌。没有p300结合能力的截短型PER2突变体失去了调节p300表达的能力,这表明PER2在调节HMGB1的乙酰化和表达中作为p300的共抑制因子发挥作用。综上所述,本研究数据揭示了一种新机制,即PER2参与控制睡眠剥夺诱导的依赖HMGB1的神经炎症。维持皮质中PER2水平或阻断HMGB1乙酰化可能是预防睡眠剥夺诱导的神经炎症及大脑相关不良反应的潜在方法。