Expression of AhR and ARNT mRNA in cultured human endometrial explants exposed to TCDD
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This study quantified AhR and ARNT mRNA expression in human endometrial explants and found TCDD treatment increased AhR mRNA, while neither gene's expression was affected by endometriosis.
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Abstract
Endometriosis is a debilitating disease found in 10-15% of reproductive-age women and is characterized by the presence of endometrial tissue outside of the uterus. The present study characterizes the expression of AhR and ARNT mRNA in a human endometrial explant culture model in the absence and presence of TCDD exposure. In a parallel, companion study using this model, TCDD exposure was shown to induce CYP1A1 mRNA, CYP1B1 mRNA, EROD (7-ethoxyresorufin-O-deethylase) activity, and CYP1B1 protein in human endometrial explants. Explants were prepared from specimens obtained at laparoscopy or laparotomy from women undergoing surgery for tubal ligation, endometriosis, or pelvic pain unrelated to endometriosis. These specimens were a subset of the specimens used in the parallel study. The explants were cultured in medium containing 10 nM estradiol (E(2)) or 1 nM estradiol plus 500 nM progesterone (E(2) + P(4)) with or without TCDD (first 24 h). After culture, AhR and ARNT mRNA expression were quantified by RT-PCR. TCDD treatment significantly increased the expression of AhR mRNA, but not ARNT mRNA. The expression of both genes was similar for all individual explants and the ratio of AhR:ARNT mRNA expression across all samples was 1.7 to 1.8. Constitutive AhR mRNA expression was donor age dependent (increasing with age), while ARNT mRNA expression was donor age and tissue phase dependent (increased in older and proliferative phase specimens). Similar to results in the parallel study on expression of CYP1A1 mRNA, CYP1B1 mRNA, EROD activity, and CYP1B1 protein, the presence of endometriosis did not affect the expression of AhR or ARNT mRNA, either constitutively or following TCDD exposure. However, the detection of disease-specific change was limited by small sample size and variability in tissue cycle phase. The human endometrial explant culture model will be useful for future studies of the effects of dioxin-like compounds on human endometrium in relationship to cycle phase, hormonal exposure, and donor age.
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Cited by (12)
- Associations between Exposure to Organochlorine Chemicals and Endometriosis: A Systematic Review of Experimental Studies and Integration of Epidemiological Evidence 2021
- Reduced microRNA-451 expression in eutopic endometrium contributes to the pathogenesis of endometriosis 2019
- Functional expression of aryl hydrocarbon receptor on mast cells populating human endometriotic tissues 2016
- Small RNA molecules in endometriosis: pathogenesis and therapeutic aspects 2014
- Environmental Influences on the Development of Endometriosis 2013
- The TP53 16-bp duplication polymorphism is enriched in endometriosis patients 2012
- Estrogen-independent actions of environmentally relevant AhR-agonists in human endometrial epithelial cells 2010
- The link between environmental toxicant exposure and endometriosis 2007
- Endometriosis: harmful survival of an ectopic tissue 2006
- Glutathione S-transferases M1/T1 gene polymorphisms and endometriosis: a meta-analysis of genetic association studies 2005
- Environmental dioxins and endometriosis 2002
- Effect of TCDD exposure on CYP1A1 and CYP1B1 expression in explant cultures of human endometrium 2001
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