| Literature DB >> 24287822 |
Kyong Hoon Kim1, Seung-min Yeon, Hyun Gyung Kim, Hyun Suk Choi, Hyojeung Kang, Hee-Deung Park, Tae Won Park, Seung Pil Pack, Eun Hee Lee, Youngjoo Byun, Sang-Eun Choi, Kenneth Sung Lee, Un-Hwan Ha, Yong Woo Jung.
Abstract
Androgen-disrupting chemicals (ADCs) can alter male sexual development. Although the effects of ADCs on hormone disruption have been studied, their influence on the immune response is not fully understood. To investigate the effects of ADCs on innate immunity, we tested eight candidate ADCs for their influence on macrophages by measuring nitric oxide (NO) production and cell viability. Our results showed that treatment with a mixture of lipopolysaccharide and hexachlorobenzene increased NO production in RAW 264.7 cells, a murine macrophage cell line. In contrast, compared to exposure to a negative control, exposure to di-2-ethylhexyl adipate (DEHA), benzylbutyl phthalate (BBP), testosterone (TTT), or permethrin decreased NO production. DEHA, BBP, and TTT inhibited NO production in an inducible nitric oxide synthase-dependent manner. Treatment with bisphenol A (BPA), nonylphenol (NNP), or tributyltin chloride (TBTC) reduced NO production and induced cell death. While BPA induced RAW 264.7 cell death through apoptosis, NNP and TBTC caused cell death through necrosis. These results offer insights into the influences of ADCs on the innate immune system.Entities:
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Year: 2014 PMID: 24287822 DOI: 10.1007/s10753-013-9781-1
Source DB: PubMed Journal: Inflammation ISSN: 0360-3997 Impact factor: 4.092