Atmospheric particulate matter aggravates cns demyelination through involvement of TLR-4/NF-kB signaling and microglial activation

• Published in: eLife 2022-02, Vol.11
• Main Authors: Han, Bing, Li, Xing, Ai, Ruo-Song, Deng, Si-Ying, Ye, Ze-Qing, Deng, Xin, Ma, Wen, Xiao, Shun, Wang, Jing-Zhi, Wang, Li-Mei, Xie, Chong, Zhang, Yan, Xu, Yan, Zhang, Yuan
• Format: Article
• Language: English
• Subjects: Air pollution; Alzheimer's disease; Animal models; Animals; Brain; CNS demyelination; Demyelinating Diseases - pathology; Demyelination; Development and progression; Epidemiology; Fetuses; Flow cytometry; Immunology and Inflammation; Inflammation; Medical research; Medicine, Experimental; Microglia; Microglia - pathology; Myelin; Nervous system; Nervous system diseases; Neurological disorders; Neuroscience; NF-kappa B; NF-κB protein; Outdoor air quality; Paralysis; Particulate matter; Particulate Matter - toxicity; Pathogenesis; Pathogenicity; Pathology; Physiological aspects; Risk factors; Spinal cord; tlr-4/nf-κb signaling; Toll-Like Receptor 4 - genetics
• ISSN: 2050-084X; 2050-084X
• DOI: 10.7554/ELIFE.72247

Atmospheric Particulate Matter (PM) is one of the leading environmental risk factors for the global burden of disease. Increasing epidemiological studies demonstrated that PM plays a significant role in CNS demyelinating disorders; however, there is no direct testimony of this, and yet the molecular mechanism by which the occurrence remains unclear. Using multiple and strategies, in the present study we demonstrate that PM exposure aggravates neuroinflammation, myelin injury, and dysfunction of movement coordination ability via boosting microglial pro-inflammatory activities, in both the pathological demyelination and physiological myelinogenesis animal models. Indeed, pharmacological disturbance combined with RNA-seq and ChIP-seq suggests that TLR-4/NF-kB signaling mediated a core network of genes that control PM-triggered microglia pathogenicity. In summary, our study defines a novel atmospheric environmental mechanism that mediates PM-aggravated microglia pathogenic activities, and establishes a systematic approach for the investigation of the effects of environmental exposure in neurologic disorders.