Wang Lu, Wei Lin Yu, Ding Ran, Feng Yanyan, Li Dongliang, Li Chaokun, Malko Philippa, Syed Mortadza Sharifah A, Wu Weidong, Yin Yaling, Jiang Lin-Hua
Sino-UK Joint Laboratory of Brain Function and Injury and Department of Physiology and Neurobiology, Xinxiang Medical University, Xinxiang, China.
School of Biomedical Sciences, Faculty of Biological Sciences, University of Leeds, Leeds, United Kingdom.
Front Physiol. 2020 Feb 26;11:155. doi: 10.3389/fphys.2020.00155. eCollection 2020.
Accumulating epidemiological evidence supports that chronic exposure to ambient fine particular matters of <2.5 μm (PM2.5) predisposes both children and adults to Alzheimer's disease (AD) and age-related brain damage leading to dementia. There is also experimental evidence to show that PM2.5 exposure results in early onset of AD-related pathologies in transgenic AD mice and development of AD-related and age-related brain pathologies in healthy rodents. Studies have also documented that PM2.5 exposure causes AD-linked molecular and cellular alterations, such as mitochondrial dysfunction, synaptic deficits, impaired neurite growth, neuronal cell death, glial cell activation, neuroinflammation, and neurovascular dysfunction, in addition to elevated levels of amyloid β (Aβ) and tau phosphorylation. Oxidative stress and the oxidative stress-sensitive TRPM2 channel play important roles in mediating multiple molecular and cellular alterations that underpin AD-related cognitive dysfunction. Documented evidence suggests critical engagement of oxidative stress and TRPM2 channel activation in various PM2.5-induced cellular effects. Here we discuss recent studies that favor causative relationships of PM2.5 exposure to increased AD prevalence and AD- and age-related pathologies, and raise the perspective on the roles of oxidative stress and the TRPM2 channel in mediating PM2.5-induced predisposition to AD and age-related brain damage.
越来越多的流行病学证据表明,长期暴露于环境中直径小于2.5微米的细颗粒物(PM2.5)会使儿童和成人都易患阿尔茨海默病(AD)以及导致痴呆的与年龄相关的脑损伤。也有实验证据表明,暴露于PM2.5会导致转基因AD小鼠出现与AD相关的病理变化提前发生,以及健康啮齿动物出现与AD相关和与年龄相关的脑病理变化。研究还记录了暴露于PM2.5会导致与AD相关的分子和细胞改变,如线粒体功能障碍、突触缺陷、神经突生长受损、神经元细胞死亡、胶质细胞活化、神经炎症和神经血管功能障碍,此外还会导致淀粉样β(Aβ)水平升高和tau蛋白磷酸化。氧化应激和对氧化应激敏感的TRPM2通道在介导多种分子和细胞改变中起重要作用,这些改变是AD相关认知功能障碍的基础。有记录的证据表明氧化应激和TRPM2通道激活在各种PM2.5诱导的细胞效应中起关键作用。在此,我们讨论了近期支持PM2.5暴露与AD患病率增加以及与AD和年龄相关的病理变化之间存在因果关系的研究,并提出了氧化应激和TRPM2通道在介导PM2.5诱导的易患AD和与年龄相关的脑损伤方面所起作用的观点。