Department of Neurology, Inselspital, University Hospital Berne, University of Berne, Berne, Switzerland.
Ann N Y Acad Sci. 2012 Jul;1261:79-87. doi: 10.1111/j.1749-6632.2012.06640.x.
Disturbances of sleep-wake rhythms are an important problem in Alzheimer's disease (AD). Circadian rhythms are regulated by clock genes. Transforming growth factor-beta (TGF-β) is overexpressed in neurons in AD and is the only cytokine that is increased in cerebrospinal fluid (CSF). Our data show that TGF-β2 inhibits the expression of the clock genes Period (Per)1, Per2, and Rev-erbα, and of the clock-controlled genes D-site albumin promoter binding protein (Dbp) and thyrotroph embryonic factor (Tef). However, our results showed that TGF-β2 did not alter the expression of brain and muscle Arnt-like protein-1 (Bmal1). The concentrations of TGF-β2 in the CSF of 2 of 16 AD patients and of 1 of 7 patients with mild cognitive impairment were in the dose range required to suppress the expression of clock genes. TGF-β2-induced dysregulation of clock genes may alter neuronal pathways, which may be causally related to abnormal sleep-wake rhythms in AD patients.
睡眠-觉醒节律紊乱是阿尔茨海默病(AD)的一个重要问题。昼夜节律受时钟基因调节。转化生长因子-β(TGF-β)在 AD 神经元中过度表达,是唯一在脑脊液(CSF)中增加的细胞因子。我们的数据表明,TGF-β2 抑制时钟基因 Period(Per)1、Per2 和 Rev-erbα,以及时钟控制基因 D-site 白蛋白启动子结合蛋白(Dbp)和甲状腺刺激胚胎因子(Tef)的表达。然而,我们的结果表明,TGF-β2 并未改变脑和肌肉芳香烃受体核转录因子样蛋白-1(Bmal1)的表达。在 16 名 AD 患者中的 2 名和 7 名轻度认知障碍患者中的 1 名患者的 CSF 中,TGF-β2 的浓度处于抑制时钟基因表达所需的剂量范围内。TGF-β2 诱导的时钟基因失调可能改变神经元途径,这可能与 AD 患者异常的睡眠-觉醒节律有因果关系。