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Polychlorinated Biphenyls (PCBS)-induced oxidative stress and inflammation in human thyrocytes: involvement of AhR and NRF-2/HO-1 pathway.
- Source :
-
Endocrine [Endocrine] 2025 Jan; Vol. 87 (1), pp. 252-261. Date of Electronic Publication: 2024 Aug 23. - Publication Year :
- 2025
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Abstract
- Purpose: In this in vitro study, we investigated the effects of polychlorinated biphenyls (PCBs) on human thyrocytes, with a focus on the involvement of AhR, a key player in xenobiotic response, and the anti-oxidant Nrf-2/HO-1 pathway.<br />Methods: Primary cultured thyrocytes were exposed to the dioxin-like congeners PCB118 and PCB126 at 2.5 and 5 µM concentrations. mRNA expression was assessed by real-time PCR, and protein expression by Western Blot and ELISA, while protein quantification was assessed by densitometric analysis.<br />Results: In cultured thyrocytes, PCB118 and PCB126 induced a significant (P < 0.01) increase of mRNA and protein levels of the pro-inflammatory cytokines IL-1beta and IL-6, while reducing those of thyroglobulin (TG) and NIS (p < 0.05), indicating down-regulation of these thyroid-specific genes in PCB-induced inflammation. ROS production also increased (p < 0.001). mRNA levels of AhR and the downstream molecules cytochrome P4501A, Nrf-2/HO-1 increased (p < 0.001), as well as related protein levels (p < 0.01), suggesting the activation of AhR and Nrf-2 pathways in response to PCBs exposure. AhR silencing decreased AhR-related gene expression and restored NIS and TG expression, while reducing inflammatory cytokines and oxidative stress markers (p < 0.05).<br />Conclusions: Dioxin-like PCBs (PCB118 and PCB126) may promote inflammation and oxidative stress in thyrocytes, impairing the expression of genes that are key players of thyroid function. These effects can be partially attributed to the activation of the AhR and Nrf-2 pathways. These data may contribute to explain the mechanisms underlying thyroid toxicity of PCBs, highlighting the potential role of these pollutants as a trigger of autoimmune thyroid inflammation and damage.<br />Competing Interests: Compliance with ethical standards. Conflict of interest: The authors declare no competing interests. Ethics approval: The study was approved by the local Ethics Committee (University of Messina) and that informed consent was obtained from the donors. The experimental procedures are in compliance with the ethical guiding principles.<br /> (© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
- Subjects :
- Humans
Cells, Cultured
Environmental Pollutants toxicity
Thyroid Gland drug effects
Thyroid Gland metabolism
Basic Helix-Loop-Helix Transcription Factors
Polychlorinated Biphenyls toxicity
NF-E2-Related Factor 2 metabolism
NF-E2-Related Factor 2 genetics
Oxidative Stress drug effects
Receptors, Aryl Hydrocarbon metabolism
Inflammation metabolism
Inflammation chemically induced
Thyroid Epithelial Cells drug effects
Thyroid Epithelial Cells metabolism
Signal Transduction drug effects
Heme Oxygenase-1 metabolism
Heme Oxygenase-1 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1559-0100
- Volume :
- 87
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Endocrine
- Publication Type :
- Academic Journal
- Accession number :
- 39174753
- Full Text :
- https://doi.org/10.1007/s12020-024-04005-w