Cellular response and extracellular vesicles characterization of human macrophages exposed to fine atmospheric particulate matter.
Air Pollutants
/ metabolism
Cell Line
Cytokines
/ metabolism
Epithelial Cells
/ metabolism
Extracellular Vesicles
/ metabolism
Gene Expression
/ drug effects
Humans
Lung
/ metabolism
Lung Diseases
/ chemically induced
Macrophages, Alveolar
/ metabolism
Oxidative Stress
Particle Size
Particulate Matter
/ metabolism
Tumor Necrosis Factor-alpha
/ metabolism
Extracellular vesicles
Fine atmospheric particulate matter
Infiltrating macrophages
Lung epithelial cells
Journal
Environmental pollution (Barking, Essex : 1987)
ISSN: 1873-6424
Titre abrégé: Environ Pollut
Pays: England
ID NLM: 8804476
Informations de publication
Date de publication:
Nov 2019
Nov 2019
Historique:
received:
14
03
2019
revised:
14
06
2019
accepted:
19
07
2019
pubmed:
6
8
2019
medline:
18
12
2019
entrez:
6
8
2019
Statut:
ppublish
Résumé
Exposure to fine atmospheric Particulate Matter (PM) is one of the major environmental causes involved in the development of inflammatory lung diseases, such as chronic obstructive pulmonary disease (COPD) or asthma. When PM is penetrating in the pulmonary system, alveolar macrophages represent the first line of defense, in particular by triggering a pro-inflammatory response, and also by their ability to recruit infiltrating macrophages from the bone marrow. The aim of this in vitro study was to evaluate the gene expression and cytokine production involved in the toxicological and inflammatory responses of infiltrating macrophages, as well as the Extracellular Vesicles (EVs) production, after their exposure to PM. The ability of these EVs to convey information related to PM exposure from exposed macrophages to pulmonary epithelial cells was also evaluated. Infiltrating macrophages respond to fine particles exposure in a conventional manner, as their exposure to PM induced the expression of Xenobiotic Metabolizing Enzymes (XMEs) such as CYP1A1 and CYP1B1, the enzymes involved in oxidative stress SOD2, NQO1 and HMOX as well as pro-inflammatory cytokines in a dose-dependent manner. Exposure to PM also induced a greater release of EVs in a dose-dependent manner. In addition, the produced EVs were able to induce a pro-inflammatory phenotype on pulmonary epithelial cells, with the induction of the release of IL6 and TNFα proinflammatory cytokines. These results suggest that infiltrating macrophages participate in the pro-inflammatory response induced by PM exposure and that EVs could be involved in this mechanism.
Identifiants
pubmed: 31382213
pii: S0269-7491(19)30963-7
doi: 10.1016/j.envpol.2019.07.101
pii:
doi:
Substances chimiques
Air Pollutants
0
Cytokines
0
Particulate Matter
0
TNF protein, human
0
Tumor Necrosis Factor-alpha
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
112933Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.