Nanoparticulate matter exposure results in neuroinflammatory changes in the corpus callosum.

Epidemiological studies have established an association between air pollution particulate matter exposure (PM2.5) and neurocognitive decline. Experimental data suggest that microglia play an essential role in air pollution PM-induced neuroinflammation and oxidative stress. This study examined the ef...

Full description

Bibliographic Details
Main Authors: Robin Babadjouni, Arati Patel, Qinghai Liu, Kristina Shkirkova, Krista Lamorie-Foote, Michelle Connor, Drew M Hodis, Hank Cheng, Constantinos Sioutas, Todd E Morgan, Caleb E Finch, William J Mack
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0206934
id doaj-1d52bae5e218486799926417ada22e48
record_format Article
spelling doaj-1d52bae5e218486799926417ada22e482021-03-03T21:15:43ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-011311e020693410.1371/journal.pone.0206934Nanoparticulate matter exposure results in neuroinflammatory changes in the corpus callosum.Robin BabadjouniArati PatelQinghai LiuKristina ShkirkovaKrista Lamorie-FooteMichelle ConnorDrew M HodisHank ChengConstantinos SioutasTodd E MorganCaleb E FinchWilliam J MackEpidemiological studies have established an association between air pollution particulate matter exposure (PM2.5) and neurocognitive decline. Experimental data suggest that microglia play an essential role in air pollution PM-induced neuroinflammation and oxidative stress. This study examined the effect of nano-sized particulate matter (nPM) on complement C5 deposition and microglial activation in the corpus callosum of mice (C57BL/6J males). nPM was collected in an urban Los Angeles region impacted by traffic emissions. Mice were exposed to 10 weeks of re-aerosolized nPM or filtered air for a cumulative 150 hours. nPM-exposed mice exhibited reactive microglia and 2-fold increased local deposition of complement C5/ C5α proteins and complement component C5a receptor 1 (CD88) in the corpus callosum. However, serum C5 levels did not differ between nPM and filtered air cohorts. These findings demonstrate white matter C5 deposition and microglial activation secondary to nPM exposure. The C5 upregulation appears to be localized to the brain.https://doi.org/10.1371/journal.pone.0206934
collection DOAJ
language English
format Article
sources DOAJ
author Robin Babadjouni
Arati Patel
Qinghai Liu
Kristina Shkirkova
Krista Lamorie-Foote
Michelle Connor
Drew M Hodis
Hank Cheng
Constantinos Sioutas
Todd E Morgan
Caleb E Finch
William J Mack
spellingShingle Robin Babadjouni
Arati Patel
Qinghai Liu
Kristina Shkirkova
Krista Lamorie-Foote
Michelle Connor
Drew M Hodis
Hank Cheng
Constantinos Sioutas
Todd E Morgan
Caleb E Finch
William J Mack
Nanoparticulate matter exposure results in neuroinflammatory changes in the corpus callosum.
PLoS ONE
author_facet Robin Babadjouni
Arati Patel
Qinghai Liu
Kristina Shkirkova
Krista Lamorie-Foote
Michelle Connor
Drew M Hodis
Hank Cheng
Constantinos Sioutas
Todd E Morgan
Caleb E Finch
William J Mack
author_sort Robin Babadjouni
title Nanoparticulate matter exposure results in neuroinflammatory changes in the corpus callosum.
title_short Nanoparticulate matter exposure results in neuroinflammatory changes in the corpus callosum.
title_full Nanoparticulate matter exposure results in neuroinflammatory changes in the corpus callosum.
title_fullStr Nanoparticulate matter exposure results in neuroinflammatory changes in the corpus callosum.
title_full_unstemmed Nanoparticulate matter exposure results in neuroinflammatory changes in the corpus callosum.
title_sort nanoparticulate matter exposure results in neuroinflammatory changes in the corpus callosum.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description Epidemiological studies have established an association between air pollution particulate matter exposure (PM2.5) and neurocognitive decline. Experimental data suggest that microglia play an essential role in air pollution PM-induced neuroinflammation and oxidative stress. This study examined the effect of nano-sized particulate matter (nPM) on complement C5 deposition and microglial activation in the corpus callosum of mice (C57BL/6J males). nPM was collected in an urban Los Angeles region impacted by traffic emissions. Mice were exposed to 10 weeks of re-aerosolized nPM or filtered air for a cumulative 150 hours. nPM-exposed mice exhibited reactive microglia and 2-fold increased local deposition of complement C5/ C5α proteins and complement component C5a receptor 1 (CD88) in the corpus callosum. However, serum C5 levels did not differ between nPM and filtered air cohorts. These findings demonstrate white matter C5 deposition and microglial activation secondary to nPM exposure. The C5 upregulation appears to be localized to the brain.
url https://doi.org/10.1371/journal.pone.0206934
work_keys_str_mv AT robinbabadjouni nanoparticulatematterexposureresultsinneuroinflammatorychangesinthecorpuscallosum
AT aratipatel nanoparticulatematterexposureresultsinneuroinflammatorychangesinthecorpuscallosum
AT qinghailiu nanoparticulatematterexposureresultsinneuroinflammatorychangesinthecorpuscallosum
AT kristinashkirkova nanoparticulatematterexposureresultsinneuroinflammatorychangesinthecorpuscallosum
AT kristalamoriefoote nanoparticulatematterexposureresultsinneuroinflammatorychangesinthecorpuscallosum
AT michelleconnor nanoparticulatematterexposureresultsinneuroinflammatorychangesinthecorpuscallosum
AT drewmhodis nanoparticulatematterexposureresultsinneuroinflammatorychangesinthecorpuscallosum
AT hankcheng nanoparticulatematterexposureresultsinneuroinflammatorychangesinthecorpuscallosum
AT constantinossioutas nanoparticulatematterexposureresultsinneuroinflammatorychangesinthecorpuscallosum
AT toddemorgan nanoparticulatematterexposureresultsinneuroinflammatorychangesinthecorpuscallosum
AT calebefinch nanoparticulatematterexposureresultsinneuroinflammatorychangesinthecorpuscallosum
AT williamjmack nanoparticulatematterexposureresultsinneuroinflammatorychangesinthecorpuscallosum
_version_ 1714817790411538432