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Environmental Levels of para-Nonylphenol Are Able to Affect Cytokine Secretion in Human Placenta

BACKGROUND: para-Nonylphenol (p-NP) is a metabolite of alkylphenols widely used in the chemical industry and manufacturing. It accumulates in the environment, where it acts with estrogen-like activity. We previously showed that p-NP acts on human placenta by inducing trophoblast differentiation and...

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Detalles Bibliográficos
Autores principales: Bechi, Nicoletta, Ietta, Francesca, Romagnoli, Roberta, Jantra, Silke, Cencini, Marco, Galassi, Gianmichele, Serchi, Tommaso, Corsi, Ilaria, Focardi, Silvano, Paulesu, Luana
Formato: Texto
Lenguaje:English
Publicado: National Institute of Environmental Health Sciences 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854774/
https://www.ncbi.nlm.nih.gov/pubmed/20194071
http://dx.doi.org/10.1289/ehp.0900882
Descripción
Sumario:BACKGROUND: para-Nonylphenol (p-NP) is a metabolite of alkylphenols widely used in the chemical industry and manufacturing. It accumulates in the environment, where it acts with estrogen-like activity. We previously showed that p-NP acts on human placenta by inducing trophoblast differentiation and apoptosis. OBJECTIVE: The aim of the present study was to investigate the effect of p-NP on cytokine secretion in human placenta. METHODS: In vitro cultures of chorionic villous explants from human placenta in the first trimester of pregnancy were treated with p-NP (10(−13), 10(−11), and 10(−9) M) in 0.1% ethanol as vehicle. Culture medium was collected after 24 hr and assayed by specific immunoassays for the cytokines granulocyte-macrophage colony-stimulating factor (GM-CSF), interferon-γ (IFN-γ), interleukin (IL)-1β, IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, and tumor necrosis factor-α (TNF-α). RESULTS: p-NP modulated cytokine secretion by inducing the release of GM-CSF, IFN-γ, IL-1β, IL-4, and IL-10, with a maximum effect at 10(−11) M. It reduced the release of TNF-α at 10(−13) M, whereas levels of IL-2 and IL-5 remained below the detection limit. IL-6 and IL-8 levels were 100–1,000 times higher than those of other cytokines, and they were not affected by p-NP. We observed significant differences from controls (ethanol alone) only for GM-CSF and IL-10. CONCLUSION: An unbalanced cytokine network at the maternal–fetal interface may result in implantation failure, pregnancy loss, or other complications. The effects of extremely low doses of p-NP on the placental release of cytokines raise considerable concerns about maternal exposure to this endocrine disruptor during pregnancy.