Literature DB >> 30912175

Exposures to the environmental contaminants pentachlorophenol and dichlorodiphenyltrichloroethane increase production of the proinflammatory cytokine, interleukin-1β, in human immune cells.

Tamara J Martin1, JaQuel Maise2, Sahra Gabure2, Margaret M Whalen2.   

Abstract

Pentachlorophenol (PCP) and dichlorodiphenyltrichloroethane (DDT) are organochlorine environmental contaminants found in human blood at very significant levels (as high as 5 μm for PCP and 260 nm for DDT). Cancers of the blood (lymphoma and myeloma) and kidney as well as others have been associated with exposure to these contaminants. Interleukin (IL)-1β is a proinflammatory cytokine and is involved in stimulating cell proliferation. High levels of IL-1β are associated with inflammatory diseases and tumor progression. Previous studies showed that PCP and DDT at certain concentrations were able to stimulate secretion of IL-1β. This study shows that the increased secretion of IL-1β seen with both contaminants is due to compound-induced increases in the production of this cytokine. Increased production began within 6 hours of exposure to PCP and continued to increase up to 24 hours. DDT-induced stimulation of IL-1β appeared to be maximal after 6 hours of exposure and then diminished by 24 hours. The increases seen in IL-1β production stimulated by PCP appear to be at least partially due to compound-induced increases in IL-1β mRNA. Although DDT caused increased production of IL-1β, it did not appear to cause consistent increases in its mRNA. PCP- and DDT-induced increases in IL-1β production were dependent primarily on the p38 mitogen-activated protein kinase pathway. These results indicate that both PCP and DDT are able to increase IL-1β production in a p38 mitogen-activated protein kinase-dependent manner, which may have the potential to influence chronic inflammation.
© 2019 John Wiley & Sons, Ltd.

Entities:  

Keywords:  MAP kinases; dichlorodiphenyltrichloroethane; immune cells; interleukin 1β; mRNA; pentachlorophenol

Year:  2019        PMID: 30912175      PMCID: PMC6625894          DOI: 10.1002/jat.3798

Source DB:  PubMed          Journal:  J Appl Toxicol        ISSN: 0260-437X            Impact factor:   3.446


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