Nakata Shinya, Iwasaki Kanako, Funato Hiromasa, Yanagisawa Masashi, Ozaki Haruka
International Institute for Integrative Sleep Medicine (WPI-IIIS), University of Tsukuba, Tsukuba, Ibaraki, Japan.
International Institute for Integrative Sleep Medicine (WPI-IIIS), University of Tsukuba, Tsukuba, Ibaraki, Japan; Department of Anatomy, Graduate School of Medicine, Toho University, Tokyo, Japan.
Neurosci Res. 2024 Oct;207:13-25. doi: 10.1016/j.neures.2024.03.004. Epub 2024 Mar 25.
Sleep is homeostatically regulated by sleep pressure, which increases during wakefulness and dissipates during sleep. Recent studies have suggested that the cerebral neocortex, a six-layered structure composed of various layer- and projection-specific neuronal subtypes, is involved in the representation of sleep pressure governed by transcriptional regulation. Here, we examined the transcriptomic changes in neuronal subtypes in the neocortex upon increased sleep pressure using single-nucleus RNA sequencing datasets and predicted the putative intracellular and intercellular molecules involved in transcriptome alterations. We revealed that sleep deprivation (SD) had the greatest effect on the transcriptome of layer 2 and 3 intratelencephalic (L2/3 IT) neurons among the neocortical glutamatergic neuronal subtypes. The expression of mutant SIK3 (SLP), which is known to increase sleep pressure, also induced profound changes in the transcriptome of L2/3 IT neurons. We identified Junb as a candidate transcription factor involved in the alteration of the L2/3 IT neuronal transcriptome by SD and SIK3 (SLP) expression. Finally, we inferred putative intercellular ligands, including BDNF, LSAMP, and PRNP, which may be involved in SD-induced alteration of the transcriptome of L2/3 IT neurons. We suggest that the transcriptome of L2/3 IT neurons is most impacted by increased sleep pressure among neocortical glutamatergic neuronal subtypes and identify putative molecules involved in such transcriptional alterations.
睡眠由睡眠压力进行稳态调节,睡眠压力在清醒期间增加,在睡眠期间消散。最近的研究表明,大脑新皮层是一种由各种层特异性和投射特异性神经元亚型组成的六层结构,参与由转录调节控制的睡眠压力的表征。在这里,我们使用单核RNA测序数据集研究了睡眠压力增加时新皮层中神经元亚型的转录组变化,并预测了参与转录组改变的假定细胞内和细胞间分子。我们发现,在新皮层谷氨酸能神经元亚型中,睡眠剥夺(SD)对第2层和第3层脑内(L2/3 IT)神经元的转录组影响最大。已知会增加睡眠压力的突变型SIK3(SLP)的表达也诱导了L2/3 IT神经元转录组的深刻变化。我们确定Junb是参与SD和SIK3(SLP)表达引起的L2/3 IT神经元转录组改变的候选转录因子。最后,我们推断了包括BDNF、LSAMP和PRNP在内的假定细胞间配体,它们可能参与SD诱导的L2/3 IT神经元转录组的改变。我们认为,在新皮层谷氨酸能神经元亚型中,L2/3 IT神经元的转录组受睡眠压力增加的影响最大,并确定了参与这种转录改变的假定分子。