MiR-7 Mediates the Zearalenone Signaling Pathway Regulating FSH Synthesis and Secretion by Targeting FOS in Female Pigs

Endocrinology. 2018 Aug 1;159(8):2993-3006. doi: 10.1210/en.2018-00097.

Abstract

Zearalenone (ZEA) acts as an environmental endocrine disruptor (EED) to cause health detriments. miRNAs were reported to influence the synthesis and secretion of pituitary hormones. However, the interactions between ZEA and miRNAs and related mechanisms remain unclear. The aims of this study were to determine whether and how miR-7 affects animal reproduction by its interactions with ZEA in the pig pituitary, which is sensitive to ZEA and has been used as an important animal model in medical research. Expressions of miRNA were detected by real-time PCR, in situ hybridization, and immunohistochemistry. The effects of ZEA, miR-7, and their interactions in the pituitary gland were identified by using an ovariectomized pig model, transfecting miR-7 mimics and inhibitor, radioimmunoassay, luciferase reporter assay, and Western blotting. The ZEA dosage was 7.5 mg/kg body weight in vivo and 1 μM in vitro. Our results demonstrate miR-7 acts to regulate gonadotropin synthesis and secretion. Furthermore, we found that ZEA leads to reproductive defects by enhancing miR-7 expression, which subsequently inhibits FSH synthesis and secretion. In vitro and in vivo experiments revealed that the effects of ZEA rely on G protein-coupled estrogen receptor 1, and miR-7 functions by mediating ZEA signaling pathway and targeting the Finkel-Biskis-Jinkins murine osteosarcoma viral oncogene homolog (FOS) gene. These findings show that miRNAs are key intrinsic factors regulating pituitary gonadotropins by mediating EED signaling in pituitary glands, and the actions of miRNAs and EEDs should be seriously considered in related studies about medical practice and animal production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Endocrine Disruptors / pharmacology
  • Estrogens, Non-Steroidal / pharmacology*
  • Female
  • Follicle Stimulating Hormone / metabolism*
  • Genes, fos / drug effects*
  • Genes, fos / genetics
  • Immunohistochemistry
  • In Situ Hybridization
  • In Vitro Techniques
  • MicroRNAs / pharmacology*
  • Ovariectomy
  • Pituitary Gland / drug effects*
  • Pituitary Gland / metabolism
  • Real-Time Polymerase Chain Reaction
  • Receptors, Estrogen / metabolism
  • Receptors, G-Protein-Coupled / metabolism
  • Signal Transduction
  • Sus scrofa
  • Swine
  • Zearalenone / pharmacology*

Substances

  • Endocrine Disruptors
  • Estrogens, Non-Steroidal
  • MicroRNAs
  • Receptors, Estrogen
  • Receptors, G-Protein-Coupled
  • Zearalenone
  • Follicle Stimulating Hormone