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Early postnatal exposure to a low dose of decabromodiphenyl ether affects expression of androgen and thyroid hormone receptor-alpha and its splicing variants in mouse Sertoli cells.

Abstract
Decabromodiphenyl ether (decaBDE) adversely affects reproduction and development. Our previous study showed that postnatal exposure to a low dose of decaBDE (0.025 mg/kg body weight/day) by subcutaneous injection on postnatal days (PNDs) 1 through 5 leads to reductions in testicular size and number of Sertoli cells and sperm, while higher dose of decaBDE (2.5 mg/kg body weight/day) had no significant differences about these. In the present study, we examined the molecular mechanism of these effects on mouse testes following postnatal exposure to a low decaBDE dose. We hypothesized that postnatal exposure to decaBDE may alter levels of serum thyroid hormones (THs) and testosterone, or the level of TH receptor alpha (Thra) transcripts and its splicing variants and androgen receptor (Ar) in Sertoli cells, adversely affecting spermatogenesis. To test this hypothesis, we examined serum TH and testosterone levels and the levels of transcripts of the Ar, Thra and its splicing variants, and Thra splicing factors (Hnrnpa1, Srsf1, and Hnrnph1) with qPCR in isolated mouse Sertoli cells exposed postnatally to decaBDE (0.025, 0.25, and 2.5 mg/kg). Levels of serum testosterone and transcripts encoding Ar, Thra, and its variant, Thra1, declined significantly in Sertoli cells of mice exposed to 0.025 mg decaBDE/kg. No significant differences in serum TH level or Thra2, Hnrnph1, or Srsf1 transcript levels were observed between control and decaBDE-exposed mice. However, the Thra1:Thra2 and Hnrnpa1:Srsf1 ratios were altered in Sertoli cells of mice exposed to 0.025 mg decaBDE/kg but not in cells exposed to 0.25 or 2.5 mg decaBDE/kg. These results indicate that postnatal exposure to a low dose of decaBDE on PNDs 1 through 5 lowers the testosterone level and the levels of Ar and Thra transcripts in Sertoli cells, accompanied by an imbalance in the ratios of Thra splicing variants, resulting in smaller testicular size and impaired spermatogenesis.
AuthorsHidenobu Miyaso, Noriko Nakamura, Munekazu Naito, Shuichi Hirai, Yoshiharu Matsuno, Masahiro Itoh, Chisato Mori
JournalPloS one (PLoS One) Vol. 9 Issue 12 Pg. e114487 ( 2014) ISSN: 1932-6203 [Electronic] United States
PMID25479311 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Halogenated Diphenyl Ethers
  • RNA-Binding Proteins
  • Receptors, Androgen
  • Thyroid Hormone Receptors alpha
  • decabromobiphenyl ether
Topics
  • Alternative Splicing (drug effects)
  • Animals
  • Halogenated Diphenyl Ethers (toxicity)
  • Male
  • Mice
  • Mice, Inbred ICR
  • RNA-Binding Proteins (metabolism)
  • Receptors, Androgen (biosynthesis)
  • Sertoli Cells
  • Thyroid Hormone Receptors alpha (biosynthesis)

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