Cargando…

Particulate Matter Exacerbates the Death of Dopaminergic Neurons in Parkinson’s Disease through an Inflammatory Response

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 dis...

Descripción completa

Detalles Bibliográficos
Autores principales: Choi, Dabin, Lee, Gaheon, Kim, Kyung Hwa, Bae, Hyunsu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9223534/
https://www.ncbi.nlm.nih.gov/pubmed/35742931
http://dx.doi.org/10.3390/ijms23126487
_version_ 1784733147934490624
author Choi, Dabin
Lee, Gaheon
Kim, Kyung Hwa
Bae, Hyunsu
author_facet Choi, Dabin
Lee, Gaheon
Kim, Kyung Hwa
Bae, Hyunsu
author_sort Choi, Dabin
collection PubMed
description 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(10): 2.5–10 μm) for short (5 days) and long (8 weeks) durations via intratracheal instillation. Long-term PM(10) 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(10) exposure resulted in both pulmonary and systemic inflammatory responses in mice. We further investigated the mechanism underlying PM(10)-induced neurotoxicity in cocultures of lung LA-4 epithelial cells and RAW264.7 macrophages. PM(10) treatment elicited a dramatic increase in proinflammatory mediators in LA-4/RAW264.7 coculture. Treating BV2 microglial cells with PM(10)-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(10)-conditioned medium. Altogether, our results demonstrated that PM(10) plays a role in the neurodegeneration associated with PD. Thus, the impact of PM(10) on neurodegeneration could be related to detrimental air pollution-induced systemic effects on the brain.
format Online
Article
Text
id pubmed-9223534
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-92235342022-06-24 Particulate Matter Exacerbates the Death of Dopaminergic Neurons in Parkinson’s Disease through an Inflammatory Response Choi, Dabin Lee, Gaheon Kim, Kyung Hwa Bae, Hyunsu Int J Mol Sci Article 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(10): 2.5–10 μm) for short (5 days) and long (8 weeks) durations via intratracheal instillation. Long-term PM(10) 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(10) exposure resulted in both pulmonary and systemic inflammatory responses in mice. We further investigated the mechanism underlying PM(10)-induced neurotoxicity in cocultures of lung LA-4 epithelial cells and RAW264.7 macrophages. PM(10) treatment elicited a dramatic increase in proinflammatory mediators in LA-4/RAW264.7 coculture. Treating BV2 microglial cells with PM(10)-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(10)-conditioned medium. Altogether, our results demonstrated that PM(10) plays a role in the neurodegeneration associated with PD. Thus, the impact of PM(10) on neurodegeneration could be related to detrimental air pollution-induced systemic effects on the brain. MDPI 2022-06-10 /pmc/articles/PMC9223534/ /pubmed/35742931 http://dx.doi.org/10.3390/ijms23126487 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Choi, Dabin
Lee, Gaheon
Kim, Kyung Hwa
Bae, Hyunsu
Particulate Matter Exacerbates the Death of Dopaminergic Neurons in Parkinson’s Disease through an Inflammatory Response
title Particulate Matter Exacerbates the Death of Dopaminergic Neurons in Parkinson’s Disease through an Inflammatory Response
title_full Particulate Matter Exacerbates the Death of Dopaminergic Neurons in Parkinson’s Disease through an Inflammatory Response
title_fullStr Particulate Matter Exacerbates the Death of Dopaminergic Neurons in Parkinson’s Disease through an Inflammatory Response
title_full_unstemmed Particulate Matter Exacerbates the Death of Dopaminergic Neurons in Parkinson’s Disease through an Inflammatory Response
title_short Particulate Matter Exacerbates the Death of Dopaminergic Neurons in Parkinson’s Disease through an Inflammatory Response
title_sort particulate matter exacerbates the death of dopaminergic neurons in parkinson’s disease through an inflammatory response
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9223534/
https://www.ncbi.nlm.nih.gov/pubmed/35742931
http://dx.doi.org/10.3390/ijms23126487
work_keys_str_mv AT choidabin particulatematterexacerbatesthedeathofdopaminergicneuronsinparkinsonsdiseasethroughaninflammatoryresponse
AT leegaheon particulatematterexacerbatesthedeathofdopaminergicneuronsinparkinsonsdiseasethroughaninflammatoryresponse
AT kimkyunghwa particulatematterexacerbatesthedeathofdopaminergicneuronsinparkinsonsdiseasethroughaninflammatoryresponse
AT baehyunsu particulatematterexacerbatesthedeathofdopaminergicneuronsinparkinsonsdiseasethroughaninflammatoryresponse