Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Via Roma 55, 56126 Pisa, Italy.
Neurology Unit, Pisa University Hospital, 56126 Pisa, Italy.
Int J Mol Sci. 2020 Nov 16;21(22):8630. doi: 10.3390/ijms21228630.
Locus Coeruleus (LC) is the main noradrenergic nucleus of the central nervous system, and its neurons widely innervate the whole brain. LC is severely degenerated both in Alzheimer's disease (AD) and in Parkinson's disease (PD), years before the onset of clinical symptoms, through mechanisms that differ among the two disorders. Several experimental studies have shown that noradrenaline modulates neuroinflammation, mainly by acting on microglia/astrocytes function. In the present review, after a brief introduction on the anatomy and physiology of LC, we provide an overview of experimental data supporting a pathogenetic role of LC degeneration in AD and PD. Then, we describe in detail experimental data, obtained in vitro and in vivo in animal models, which support a potential role of neuroinflammation in such a link, and the specific molecules (i.e., released cytokines, glial receptors, including pattern recognition receptors and others) whose expression is altered by LC degeneration and might play a key role in AD/PD pathogenesis. New imaging and biochemical tools have recently been developed in humans to estimate in vivo the integrity of LC, the degree of neuroinflammation, and pathology AD/PD biomarkers; it is auspicable that these will allow in the near future to test the existence of a link between LC-neuroinflammation and neurodegeneration directly in patients.
蓝斑(LC)是中枢神经系统的主要去甲肾上腺素能核团,其神经元广泛支配整个大脑。LC 在阿尔茨海默病(AD)和帕金森病(PD)中都严重退化,早在临床症状出现之前,其退化的机制在两种疾病中有所不同。几项实验研究表明,去甲肾上腺素通过作用于小胶质细胞/星形胶质细胞的功能来调节神经炎症。在本综述中,在简要介绍 LC 的解剖和生理学之后,我们概述了支持 LC 退化在 AD 和 PD 发病机制中起致病作用的实验数据。然后,我们详细描述了在体外和动物模型中获得的实验数据,这些数据支持神经炎症在这种联系中的潜在作用,以及 LC 退化改变其表达的特定分子(即释放的细胞因子、神经胶质受体,包括模式识别受体等)可能在 AD/PD 发病机制中发挥关键作用。最近在人类中开发了新的成像和生化工具来估计 LC 的完整性、神经炎症的程度和 AD/PD 生物标志物的病理;有望在不久的将来直接在患者中测试 LC-神经炎症与神经退行性变之间的联系是否存在。