LH signaling induced ptgs2a expression is required for ovulation in zebrafish

Mol Cell Endocrinol. 2017 May 15:447:125-133. doi: 10.1016/j.mce.2017.02.042. Epub 2017 Feb 28.

Abstract

It is well known that ovulation is induced by luteinizing hormone (LH) surge. However, the down-stream factors that mediating LH surge induced ovulation are less clear. The cyclooxygenases (also known as PTGS) as key enzymes for prostaglandins synthesis appear to be important for ovulation in mammals, but their functional roles and molecular mechanism in regulation of fish ovulation are largely unexplored. In this study, we have systematically investigated the expression, regulation and functional roles of cox genes during zebrafish ovulation. Three types of cox genes including ptgs1, ptgs2a and ptgs2b have been identified in zebrafish. The ptgs2a was dominantly expressed in the ovary with a maximal level at the maturation stage of the follicles. In addition, the ptgs2a expression is up-regulated by LH signaling in vitro and in vivo. Moreover, co-injection of a selective Ptgs2 inhibitor and non-selective Ptgs inhibitor with hCG could significantly block the stimulatory effect of hCG induced ovulation in vivo. Collectively, our findings indicate that LH signaling induced ptgs2a expression is required for ovulation in zebrafish.

Keywords: LH; Ovulation; PG; Ptgs; Zebrafish.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Chorionic Gonadotropin / pharmacology
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism*
  • Cyclooxygenase Inhibitors / pharmacology
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation / drug effects
  • Humans
  • Luteinizing Hormone / pharmacology*
  • Oocytes / cytology
  • Oocytes / drug effects
  • Oocytes / metabolism
  • Ovarian Follicle / drug effects
  • Ovarian Follicle / metabolism
  • Ovulation / drug effects*
  • Signal Transduction* / drug effects
  • Zebrafish / metabolism*

Substances

  • Chorionic Gonadotropin
  • Cyclooxygenase Inhibitors
  • Luteinizing Hormone
  • Cyclooxygenase 2