Metabolic Response of RAW 264.7 Macrophages to Exposure to Crude Particulate Matter and a Reduced Content of Organic Matter.

cell viability nitric oxide particulate matter reactive oxygen species

Journal

Toxics
ISSN: 2305-6304
Titre abrégé: Toxics
Pays: Switzerland
ID NLM: 101639637

Informations de publication

Date de publication:
30 Aug 2021
Historique:
received: 13 07 2021
revised: 26 08 2021
accepted: 27 08 2021
entrez: 26 9 2021
pubmed: 27 9 2021
medline: 27 9 2021
Statut: epublish

Résumé

Exposure to air pollution from various airborne particulate matter (PM) is regarded as a potential health risk. Airborne PM penetrates the lungs, where it is taken up by macrophages, what results in macrophage activation and can potentially lead to negative consequences for the organism. In the present study, we assessed the effects of direct exposure of RAW 264.7 macrophages to crude PM (NIST1648a) and to a reduced content of organic matter (LAp120) for up to 72 h on selected parameters of metabolic activity. These included cell viability and apoptosis, metabolic activity and cell number, ROS synthesis, nitric oxide (NO) release, and oxidative burst. The results indicated that both NIST1648a and LAp120 negatively influenced the parameters of cell viability and metabolic activity due to increased ROS synthesis. The negative effect of PM was concentration-dependent; i.e., it was the most pronounced for the highest concentration applied. The impact of PM also depended on the time of exposure, so at respective time points, PM induced different effects. There were also differences in the impact of NIST1648a and LAp120 on almost all parameters tested. The negative effect of LAp120 was more pronounced, what appeared to be associated with an increased content of metals.

Identifiants

pubmed: 34564356
pii: toxics9090205
doi: 10.3390/toxics9090205
pmc: PMC8472964
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : National Science Centre, Poland
ID : 2015/16/W/ST5/00005

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Auteurs

Monika Jankowska-Kieltyka (M)

Department of Brain Biochemistry, Maj Institute of Pharmacology, Polish Academy of Sciences, Smętna Street 12, 31-343 Kraków, Poland.

Adam Roman (A)

Department of Brain Biochemistry, Maj Institute of Pharmacology, Polish Academy of Sciences, Smętna Street 12, 31-343 Kraków, Poland.

Magdalena Mikrut (M)

Faculty of Chemistry, Jagiellonian University, Gronostajowa Street 2, 30-387 Kraków, Poland.

Marta Kowalska (M)

Department of Brain Biochemistry, Maj Institute of Pharmacology, Polish Academy of Sciences, Smętna Street 12, 31-343 Kraków, Poland.

Rudi van Eldik (R)

Faculty of Chemistry, Jagiellonian University, Gronostajowa Street 2, 30-387 Kraków, Poland.
Department of Chemistry and Pharmacy, University of Erlangen-Nuremberg, Egerlandstr. 1, 91058 Erlangen, Germany.

Irena Nalepa (I)

Department of Brain Biochemistry, Maj Institute of Pharmacology, Polish Academy of Sciences, Smętna Street 12, 31-343 Kraków, Poland.

Classifications MeSH