生物质燃料通过星形胶质细胞IL-17A/IL-17RA通路诱导神经炎症和神经变性

IF 11.3 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL
Fengchu Liang, Zongtang Xu, Liuyan Ding, Ziting Zhu, Minshan Chen, Hui Shu, Xingting Huang, Zhongqiang Su, Xiaobei Wang, Yousheng Xiao, Shuxuan Huang, Dongmei Mai, Erkang Yi, Pingyi Xu, Wenlong Zhang
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引用次数: 0

摘要

已知生物质燃料(BMF)暴露会引起呼吸道炎症,但其对中枢神经系统(CNS)的影响及其潜在机制尚不清楚。BMF燃烧释放颗粒物(PM2.5),引发全身性炎症,这与帕金森病(PD)等神经退行性疾病的风险增加有关。本研究表明,长时间暴露于BMF会导致小鼠多巴胺能神经元丢失,α-突触核蛋白(α-syn)磷酸化增加,神经炎症,导致运动和认知障碍。在机制上,BMF激活外周的白细胞介素- 17a (IL-17A)信号通路,促进Th细胞穿过血脑屏障浸润,刺激星形胶质细胞释放IL-17A,激活小胶质细胞上的IL-17受体A (IL-17RA)。转录组学和代谢组学分析显示,BMF暴露显著破坏免疫和神经递质途径。重要的是,IL-17A敲除(IL-17A-/-)小鼠在BMF暴露后表现出明显的运动和认知功能改善和神经炎症减少。这些发现表明IL-17A是肺脑轴的关键介质,在中枢神经系统和周围神经系统中协调pd相关的免疫反应。IL-17A途径是PD和与环境污染物暴露相关的神经炎症变化的有希望的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Biomass Fuel Induces Neuroinflammation and Neurodegeneration via the AstrocyteMicroglia IL-17A/IL-17RA Pathway

Biomass Fuel Induces Neuroinflammation and Neurodegeneration via the AstrocyteMicroglia IL-17A/IL-17RA Pathway
Biomass fuel (BMF) exposure is known to cause respiratory inflammation, but its impact on the central nervous system (CNS) and the mechanisms underlying this effect remain unclear. BMF combustion releases particulate matter (PM2.5), triggering systemic inflammation, which is linked to an increased risk of neurodegenerative diseases such as Parkinson’s disease (PD). This study revealed that prolonged BMF exposure leads to dopaminergic neuron loss, increased α-synuclein (α-syn) phosphorylation, and neuroinflammation, resulting in motor and cognitive impairments in mice. Mechanistically, BMF activates the interleukin-17A (IL-17A) signalling pathway in the periphery, promoting Th cell infiltration across the bloodsingle bondbrain barrier, which stimulates astrocytes to release IL-17A and activates IL-17 receptor A (IL-17RA) on microglia. Transcriptomic and metabolomic analyses revealed that BMF exposure significantly disrupts immune and neurotransmitter pathways. Importantly, IL-17A knockout (IL-17A-/-) mice exhibit marked improvements in motor and cognitive functions and reduced neuroinflammation following BMF exposure. These findings identify IL-17A as a critical mediator of the lungsingle bondbrain axis, orchestrating PD-related immune responses within both the CNS and peripheral nervous system. The IL-17A pathway represents a promising therapeutic target for PD and the related neuroinflammatory changes associated with environmental pollutant exposure.
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来源期刊
Journal of Hazardous Materials
Journal of Hazardous Materials 工程技术-工程:环境
CiteScore
25.40
自引率
5.90%
发文量
3059
审稿时长
58 days
期刊介绍: The Journal of Hazardous Materials serves as a global platform for promoting cutting-edge research in the field of Environmental Science and Engineering. Our publication features a wide range of articles, including full-length research papers, review articles, and perspectives, with the aim of enhancing our understanding of the dangers and risks associated with various materials concerning public health and the environment. It is important to note that the term "environmental contaminants" refers specifically to substances that pose hazardous effects through contamination, while excluding those that do not have such impacts on the environment or human health. Moreover, we emphasize the distinction between wastes and hazardous materials in order to provide further clarity on the scope of the journal. We have a keen interest in exploring specific compounds and microbial agents that have adverse effects on the environment.
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