The Extracellular Calcium-Sensing Receptor (CASR) Regulates Gonadotropins-Induced Meiotic Maturation of Porcine Oocytes

Biol Reprod. 2015 Dec;93(6):131. doi: 10.1095/biolreprod.115.128579. Epub 2015 Oct 21.

Abstract

Gonadotropins and epidermal growth factor (EGF) play crucial roles in promoting oocyte maturation. The regulatory network downstream of these key factors is not well understood. The present study was designed to investigate the role of the calcium-sensing receptor (CASR) in porcine oocyte in vitro maturation. CASR expression was up-regulated in oocytes matured in gonadotropin-containing medium. Cortical distribution of CASR was enhanced with gonadotropins but not EGF. Supplementation of a CASR agonist (NPS R-568) in the gonadotropin (FSH and/or LH)-containing maturation medium significantly enhanced oocyte nuclear maturation. Addition of NPS2390, a CASR antagonist, compromised oocyte nuclear maturation. Furthermore, increased cortical distribution and decreased expression of CASR was observed after the NPS R-568 treatment. Oocytes treated with NPS R-568 had higher concentration of CYCLIN B1, decreased reactive oxygen species, and increased glutathione levels, indicative of advanced cytoplasmic maturation. In contrast, NPS2390 treatment compromised oocyte cytoplasmic maturation. A higher blastocyst formation rate after parthenogenetic activation was observed when oocytes were matured in the presence of the CASR agonist, NPS R-568. MAPK3/1 phosphorylation was increased during in vitro maturation and after NPS R-568 treatment, and decreased following CASR antagonist supplementation. Taken together, our data showed that the CASR is a gonadotropin-regulated factor that promotes porcine oocyte maturation in a MAPK-dependent manner.

Keywords: EGF; MAPK; calcium-sensing receptor; gonadotropins; maturation.

MeSH terms

  • Animals
  • Cyclin B1 / metabolism
  • Female
  • Follicle Stimulating Hormone / pharmacology
  • Glutathione / metabolism
  • Luteinizing Hormone / pharmacology
  • MAP Kinase Signaling System / drug effects
  • MAP Kinase Signaling System / physiology*
  • Meiosis / drug effects
  • Meiosis / physiology*
  • Oocytes / drug effects
  • Oocytes / metabolism*
  • Phenethylamines / pharmacology
  • Propylamines / pharmacology
  • Reactive Oxygen Species / metabolism
  • Receptors, Calcium-Sensing / agonists
  • Receptors, Calcium-Sensing / genetics
  • Receptors, Calcium-Sensing / metabolism*
  • Swine
  • Up-Regulation

Substances

  • Cyclin B1
  • N-(2-chlorophenylpropyl)-1-(3-methoxyphenyl)ethylamine
  • Phenethylamines
  • Propylamines
  • Reactive Oxygen Species
  • Receptors, Calcium-Sensing
  • Luteinizing Hormone
  • Follicle Stimulating Hormone
  • Glutathione