Cdkl5 Knockout Mice Recapitulate Sleep Phenotypes of CDKL5 Deficient Disorder

被引:0
作者
Cao, Liqin [1 ,2 ]
Zhang, Xin [1 ]
Lou, Tingting [1 ]
Ma, Jing [1 ,3 ]
Wang, Zhiqiang [1 ,3 ]
Kim, Staci J. [1 ,4 ]
Vogt, Kaspar [1 ]
Hirano, Arisa [1 ]
Tanaka, Teruyuki [5 ,6 ]
Kikkawa, Yoshiaki [2 ]
Yanagisawa, Masashi [1 ]
Liu, Qinghua [1 ,7 ,8 ]
机构
[1] Univ Tsukuba, Int Inst Integrat Sleep Med WPI IIIS, Tsukuba, Ibaraki 3058575, Japan
[2] Tokyo Metropolitan Inst Med Sci, Dept Basic Med Sci, Deafness Project, Tokyo 1568506, Japan
[3] Harbin Inst Technol, HIT Ctr Life Sci HCLS, Sch Life Sci & Technol, Harbin 150001, Peoples R China
[4] Korea Adv Inst Sci & Technol, Dept Brain & Cognit Sci, Daejeon 34141, South Korea
[5] Tokyo Children Rehabil Hosp, Tokyo 2080011, Japan
[6] Univ Tokyo, Grad Sch Med, Dept Dev Med Sci, Tokyo 1130033, Japan
[7] Natl Inst Biol Sci NIBS, Beijing 102206, Peoples R China
[8] Tsinghua Univ, Tsinghua Inst Multidisciplinary Biomed Res TIMBR, Beijing 100084, Peoples R China
关键词
CDKL5; mouse models; sleep; electroencephalography (EEG); circuit function; MOUSE MODEL; REM-SLEEP; IMPAIRMENT; BIOMARKERS; CHILDREN; PHASE;
D O I
10.3390/ijms26083754
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 Cdkl5 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. Cdkl5 KO mice exhibited pre-sleep arousal, but normal circadian rhythm and homeostatic sleep response. Conditional knockout (cKO) of Cdkl5 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 Cdkl5 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.
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