» Articles » PMID: 19337519

Activated Toxicity of Diesel Particulate Extract by Ultraviolet a Radiation in Mammalian Cells: Role of Singlet Oxygen

Overview
Date 2009 Apr 2
PMID 19337519
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Diesel exhaust [diesel exhaust particles (DEPs) and their extracts (DPE)] and ultraviolet A radiation (UVA) are two ubiquitous environmental factors that have been identified as essential risk factors for various benign or malignant human diseases, either alone or in combination with other agents.

Objectives: We aimed to investigate the synergistic effects of DPE and UVA at low-dose exposures in human-hamster hybrid (AL) cells and their underlying mechanisms.

Methods: We exposed exponentially growing AL cells to DPE and/or UVA radiation with or without reactive oxygen species (ROS) quenchers and then assayed the cells for survival, mutation induction, apoptosis, and micronucleus generation. In addition, using a singlet oxygen (1O2) trapping probe, 2,2,6,6-tetramethyl-4-piperidone, coupled with electron paramagnetic resonance spectroscopy, we determined the production of 1O2.

Results: Treatment of AL cells with DPE+UVA induced significant cytotoxic and genotoxic damage. In contrast, we found no significant damage in cells treated with either UVA or DPE alone at the same doses. Mutation spectra of CD59- mutants showed that treatment with DPE+UVA easily induces multilocus deletions. Sodium azide significantly inhibited both cellular and DNA damage induced by DPE+UVA treatment, whereas other ROS inhibitors had little protecting effect. Furthermore, we found a significant increase of 1O2 in the cells that received DPE+UVA treatment.

Conclusion: These findings suggest that UVA activated the genotoxicity and cytotoxicity of DPE in mammalian cells and that 1O2 played an important role in these processes.

Citing Articles

Ultraviolet Light Protection: Is It Really Enough?.

Farris P, Valacchi G Antioxidants (Basel). 2022; 11(8).

PMID: 36009203 PMC: 9405175. DOI: 10.3390/antiox11081484.


Determination of the Phototoxicity Potential of Commercially Available Tattoo Inks Using the 3T3-neutral Red Uptake Phototoxicity Test.

Utku Turk E, Jannuzzi A, Alpertunga B Turk J Pharm Sci. 2022; 19(1):70-75.

PMID: 35227052 PMC: 8892553. DOI: 10.4274/tjps.galenos.2021.86344.


Mechanisms underlying the health effects of desert sand dust.

Fussell J, Kelly F Environ Int. 2021; 157:106790.

PMID: 34333291 PMC: 8484861. DOI: 10.1016/j.envint.2021.106790.


Diesel exhaust particles induce toxicity to beta cells by suppressing miR-140-5p.

Du Y, Liu J, Zhu Y, Yuan X, Gao J, Cheng J Int J Clin Exp Pathol. 2020; 12(8):2858-2866.

PMID: 31934122 PMC: 6949722.


Air Pollution and Skin Aging.

Schikowski T, Huls A Curr Environ Health Rep. 2020; 7(1):58-64.

PMID: 31927691 DOI: 10.1007/s40572-020-00262-9.


References
1.
DeMarini D, Brooks L, Warren S, Kobayashi T, Gilmour M, Singh P . Bioassay-directed fractionation and salmonella mutagenicity of automobile and forklift diesel exhaust particles. Environ Health Perspect. 2004; 112(8):814-9. PMC: 1242006. DOI: 10.1289/ehp.6578. View

2.
Sato H, Sone H, Sagai M, Suzuki K, Aoki Y . Increase in mutation frequency in lung of Big Blue rat by exposure to diesel exhaust. Carcinogenesis. 2000; 21(4):653-61. DOI: 10.1093/carcin/21.4.653. View

3.
Ohnishi S, Kawanishi S . Double base lesions of DNA by a metabolite of carcinogenic benzo[a]pyrene. Biochem Biophys Res Commun. 2002; 290(2):778-82. DOI: 10.1006/bbrc.2001.6249. View

4.
Zang L, Van Kuijk F, Misra B, Misra H . The specificity and product of quenching singlet oxygen by 2,2,6,6-tetramethylpiperidine. Biochem Mol Biol Int. 1995; 37(2):283-93. View

5.
Yin L, Morita A, Tsuji T . Skin aging induced by ultraviolet exposure and tobacco smoking: evidence from epidemiological and molecular studies. Photodermatol Photoimmunol Photomed. 2001; 17(4):178-83. DOI: 10.1034/j.1600-0781.2001.170407.x. View