2, 3, 7, 8-Tetrachlorodibenzo-p-dioxin potential impacts on peripheral blood mononuclear cells of endometriosis women. (February 2022)
- Record Type:
- Journal Article
- Title:
- 2, 3, 7, 8-Tetrachlorodibenzo-p-dioxin potential impacts on peripheral blood mononuclear cells of endometriosis women. (February 2022)
- Main Title:
- 2, 3, 7, 8-Tetrachlorodibenzo-p-dioxin potential impacts on peripheral blood mononuclear cells of endometriosis women
- Authors:
- Tanha, Mahsa
Bozorgmehr, Mahmood
Shokri, Mohammad-Reza
Edalatkhah, Haleh
Tanha, Mahya
Zarnani, Amir-Hassan
Nikoo, Shohreh - Abstract:
- Highlights: PBMCs of endometriosis patients express lower levels of AHR and IDO1 genes compared to those of normal individuals. TCDD increases the expression of AHR, IDO1 and FOXP3 genes in endometriosis compared to non-endometriosis PBMCs. In response to TCDD treatment, endometriosis PBMCs produce higher levels of kynurenine and IL-6. Abstract: Endometriosis happens following the implantation of endometrial-derived tissues outside the uterine cavity. It has been suggested that 2, 3, 7, 8-Tetrachlorodibenzo-p-dioxin (TCDD) is involved in endometriosis development. Furthermore, aryl hydrocarbon receptor (AHR), as a TCDD receptor, has been demonstrated to regulate immune responses. Nonetheless, data regarding the mechanisms, through which TCDD influences the immune system in endometriosis, are still inconclusive. Therefore, frequency of regulatory T cells (Tregs) and the expression of FOXP3, AHR and indoleamine 2, 3-dioxygenase 1 ( IDO1 ) from endometriosis and non-endometriosis individuals were investigated in the absence and presence of TCDD; also, the concentration of IL-6 and kynurenine in the supernatant of cultures was assessed. The impact of TCDD-treated PBMCs on the migration capacity of menstrual blood-derived stromal stem cells (MenSCs) and monocyte chemoattractant protein-1 (MCP-1) and IL-6 production was determined. Here, we found that AHR and IDO1 expression levels were lower in endometriosis PBMCs; however, TCDD treatment increased AHR, FOXP3, IDO1, IL-6, andHighlights: PBMCs of endometriosis patients express lower levels of AHR and IDO1 genes compared to those of normal individuals. TCDD increases the expression of AHR, IDO1 and FOXP3 genes in endometriosis compared to non-endometriosis PBMCs. In response to TCDD treatment, endometriosis PBMCs produce higher levels of kynurenine and IL-6. Abstract: Endometriosis happens following the implantation of endometrial-derived tissues outside the uterine cavity. It has been suggested that 2, 3, 7, 8-Tetrachlorodibenzo-p-dioxin (TCDD) is involved in endometriosis development. Furthermore, aryl hydrocarbon receptor (AHR), as a TCDD receptor, has been demonstrated to regulate immune responses. Nonetheless, data regarding the mechanisms, through which TCDD influences the immune system in endometriosis, are still inconclusive. Therefore, frequency of regulatory T cells (Tregs) and the expression of FOXP3, AHR and indoleamine 2, 3-dioxygenase 1 ( IDO1 ) from endometriosis and non-endometriosis individuals were investigated in the absence and presence of TCDD; also, the concentration of IL-6 and kynurenine in the supernatant of cultures was assessed. The impact of TCDD-treated PBMCs on the migration capacity of menstrual blood-derived stromal stem cells (MenSCs) and monocyte chemoattractant protein-1 (MCP-1) and IL-6 production was determined. Here, we found that AHR and IDO1 expression levels were lower in endometriosis PBMCs; however, TCDD treatment increased AHR, FOXP3, IDO1, IL-6, and Treg levels in the endometriosis group (P ≤ 0.05−0.0001). TCDD-treated PBMCs increased the migration capacity of MenSCs and up-regulated MCP-1 and IL-6 levels in the PBMCs/MenSCs co-culture (P ≤ 0.01−0.0001). In conclusion, these results shed light on the probable mechanisms, through which AHR activation by chemical toxicants can impact inflammatory immune mediators involved in the development of endometriosis; also, these data support the idea that TCDD could promote endometriosis progression. … (more)
- Is Part Of:
- Journal of reproductive immunology. Volume 149(2022)
- Journal:
- Journal of reproductive immunology
- Issue:
- Volume 149(2022)
- Issue Display:
- Volume 149, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 149
- Issue:
- 2022
- Issue Sort Value:
- 2022-0149-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-02
- Subjects:
- Tregs regulatory T cells -- TCDD 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin -- AHR aryl hydrocarbon receptor -- IDO1 indoleamine 2, 3-dioxygenase 1 -- Trp tryptophan -- Kyn kynurenine -- TNF-α tumor necrosis factor-α -- VEGF vascular endothelial growth factor -- MCP-1 monocyte chemoattractant protein-1 -- PBMCs peripheral blood mononuclear cells -- MenSCs menstrual blood stromal stem cells -- NSAIDs nonsteroidal anti-inflammatory drugs -- OCCs organochlorine chemicals -- EAE experimental autoimmune encephalomyelitis
Endometriosis -- Regulatory T cells (Tregs) -- 2, 3, 7, 8-Tetrachlorodibenzo-p-dioxin (TCDD) -- Aryl hydrocarbon receptor (AHR) -- Indoleamine 2, 3-dioxygenase 1 (IDO1)
Reproduction -- Immunological aspects -- Periodicals
Immunology -- Periodicals
Allergy and Immunology -- Periodicals
Reproduction -- Periodicals
Reproduction -- Immunologie -- Périodiques
Immunologie -- Périodiques
Immunology
Reproduction -- Immunological aspects
Periodicals
Electronic journals
Electronic journals
615.766 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01650378 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jri.2021.103439 ↗
- Languages:
- English
- ISSNs:
- 0165-0378
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- Legaldeposit
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