Cao Liqin, Zhang Xin, Lou Tingting, Ma Jing, Wang Zhiqiang, Kim Staci J, Vogt Kaspar, Hirano Arisa, Tanaka Teruyuki, Kikkawa Yoshiaki, Yanagisawa Masashi, Liu Qinghua
International Institute for Integrative Sleep Medicine (WPI-IIIS), University of Tsukuba, Tsukuba 305-8575, Japan.
Deafness Project, Department of Basic Medical Sciences, Tokyo Metropolitan Institute of Medical Science, Tokyo 156-8506, Japan.
Int J Mol Sci. 2025 Apr 16;26(8):3754. doi: 10.3390/ijms26083754.
Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is an X-linked rare neurodevelopmental disorder associated with severe sleep disturbances. However, little is known about the mechanisms underlying sleep disturbances in CDD patients. Here, we employed the electroencephalogram (EEG) recording to characterize sleep-wake behaviors and EEG activity in male CDKL5-deficient mice. We found that young adult and middle-aged knockout (KO) mice recapitulated sleep phenotypes in patients with CDD, including difficulties in initiating and maintaining sleep, reduction in total sleep time, and frequent night awakenings. KO mice exhibited pre-sleep arousal, but normal circadian rhythm and homeostatic sleep response. Conditional knockout (cKO) of in glutamatergic neurons resulted in reduced sleep time and difficulty in sleep maintenance. Further, the rate of age-associated decline in sleep and EEG activity in KO mice was comparable to that of wild-type littermates. Together, these results confirm a causative role for CDKL5 deficiency in sleep disturbances observed in CDD patients and establish an animal model for translational research of sleep treatment in CDD. Moreover, our results provide valuable information for developing therapeutic strategies and identifying sleep and EEG parameters as potential biomarkers for facilitating preclinical and clinical trials in CDD.
细胞周期蛋白依赖性激酶样5(CDKL5)缺乏症(CDD)是一种与严重睡眠障碍相关的X连锁罕见神经发育障碍。然而,对于CDD患者睡眠障碍的潜在机制知之甚少。在这里,我们采用脑电图(EEG)记录来表征雄性CDKL5缺陷小鼠的睡眠-觉醒行为和EEG活动。我们发现,年轻成年和中年基因敲除(KO)小鼠重现了CDD患者的睡眠表型,包括入睡和维持睡眠困难、总睡眠时间减少以及频繁夜间觉醒。KO小鼠表现出睡前觉醒,但昼夜节律和稳态睡眠反应正常。谷氨酸能神经元中的条件性基因敲除(cKO)导致睡眠时间减少和睡眠维持困难。此外,KO小鼠睡眠和EEG活动随年龄下降的速率与野生型同窝小鼠相当。总之,这些结果证实了CDKL5缺乏在CDD患者中观察到的睡眠障碍中的致病作用,并建立了一个用于CDD睡眠治疗转化研究的动物模型。此外,我们的结果为制定治疗策略以及确定睡眠和EEG参数作为潜在生物标志物以促进CDD的临床前和临床试验提供了有价值的信息。