Genetic background and window of exposure contribute to thyroid dysfunction promoted by low-dose exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin in mice

• Published in: Scientific reports 2018-11, Vol.8 (1), p.16324-11, Article 16324
• Main Authors: Reale, Carla, Porreca, Immacolata, Russo, Filomena, Marotta, Maria, Roberto, Luca, Russo, Nicola Antonino, Carchia, Emanuele, Mallardo, Massimo, De Felice, Mario, Ambrosino, Concetta
• Format: Article
• Language: English
• Subjects: 14/63; 38; 38/77; 38/90; 64/60; 692/163/2743/1841; 692/499; 704/172/4081; 82; 82/29; 82/51; 82/80; Dioxins; Environmental factors; Exposure; Haploinsufficiency; Humanities and Social Sciences; Hypothyroidism; multidisciplinary; p53 Protein; Pax8 protein; Prenatal exposure; Science; Science (multidisciplinary); TCDD; Thyroid; Thyroid diseases; Thyroid gland; Thyroid transcription factor 1
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-34427-2

Genetic and environmental factors contribute to thyroid diseases. Although still debated, 2,3,7,8-tetrachlorodibenzo- p -dioxin (TCDD) is thought to induce thyroid dysfunction in humans and rodents. The data here reported point out the contribution of the exposure window and genetic background in mediating the low-dose TCDD effects on thyroid. Indeed, early (from E0.5 to PND30) and low-dose (0,001 μg/kg/day) TCDD exposure reduced the circulating fT4 and altered the expression of thyroid specific transcripts. The role of genetic components was estimated monitoring the same markers in Pax8 +/− and Nkx2-1 +/− mice, susceptible to thyroid dysfunction, exposed to 0, 1 μg/kg/day TCDD from E15.5 to PND60. Haploinsufficiency of either Pax8 or Nkx2-1 genes exacerbated the effects of the exposure impairing the thyroid enriched mRNAs in sex dependent manner. Such effect was mediated by mechanisms involving the Nkx2-1/p53/p65/IĸBα pathway in vitro and in vivo . Foetal exposure to TCDD impaired both thyroid function and genes expression while thyroid development and differentiation did not appear significantly affected. In mouse, stronger effects were related to earlier exposure or specific genetic background such as either Pax8 or Nkx2-1 haploinsufficiency, both associated to hypothyroidism in humans. Furthermore, our data underline that long exposure time are needed to model in vitro and in vivo results.