Department of Physiology, College of Korean Medicine, Kyung Hee University, 26-6 Kyungheedae-ro, Dongdaemoon-gu, Seoul 02453, Korea.
Department of Health Sciences, The Graduate School of Dong-A University, 840 Hadan-dong, Saha-gu, Busan 49315, Korea.
Int J Mol Sci. 2022 Jun 10;23(12):6487. doi: 10.3390/ijms23126487.
Particulate matter (PM), a component of air pollution, has been epidemiologically associated with a variety of diseases. Recent reports reveal that PM has detrimental effects on the brain. In this study, we aimed to investigate the biological effects of ambient particles on the neurodegenerative disease Parkinson's disease (PD). We exposed mice to coarse particles (PM: 2.5-10 μm) for short (5 days) and long (8 weeks) durations via intratracheal instillation. Long-term PM exposure exacerbated motor impairment and dopaminergic neuron death in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced PD mouse models. Short-term PM exposure resulted in both pulmonary and systemic inflammatory responses in mice. We further investigated the mechanism underlying PM-induced neurotoxicity in cocultures of lung LA-4 epithelial cells and RAW264.7 macrophages. PM treatment elicited a dramatic increase in proinflammatory mediators in LA-4/RAW264.7 coculture. Treating BV2 microglial cells with PM-treated conditioned medium induced microglial activation. Furthermore, 1-methyl-4-phenylpyridinium (MPP) treatment caused notable cell death in N2A neurons cocultured with activated BV2 cells in PM-conditioned medium. Altogether, our results demonstrated that PM plays a role in the neurodegeneration associated with PD. Thus, the impact of PM on neurodegeneration could be related to detrimental air pollution-induced systemic effects on the brain.
颗粒物(PM)是空气污染的一个组成部分,已在流行病学上与多种疾病相关联。最近的报告显示,PM 对大脑有不利影响。在这项研究中,我们旨在研究环境颗粒物对神经退行性疾病帕金森病(PD)的生物学影响。我们通过气管内滴注使小鼠短期(5 天)和长期(8 周)暴露于粗颗粒物(PM:2.5-10μm)中。长期 PM 暴露加剧了 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的 PD 小鼠模型中的运动障碍和多巴胺能神经元死亡。短期 PM 暴露导致小鼠肺部和全身炎症反应。我们进一步研究了 PM 诱导的肺 LA-4 上皮细胞和 RAW264.7 巨噬细胞共培养物中神经毒性的机制。PM 处理引起 LA-4/RAW264.7 共培养物中促炎介质的急剧增加。用 PM 处理的条件培养基处理 BV2 小胶质细胞可诱导小胶质细胞活化。此外,用 PM 处理的条件培养基中激活的 BV2 细胞共培养的 N2A 神经元中,MPP 处理可导致明显的细胞死亡。总之,我们的研究结果表明 PM 参与了与 PD 相关的神经退行性变。因此,PM 对神经退行性变的影响可能与有害的空气污染对大脑的全身影响有关。