The calcium-sensing receptor regulates protein tyrosine phosphorylation through PDK1 in boar spermatozoa

Mol Reprod Dev. 2019 Jul;86(7):751-761. doi: 10.1002/mrd.23160. Epub 2019 May 9.

Abstract

Regulation of protein tyrosine phosphorylation is required for sperm capacitation and oocyte fertilization. The objective of the present work was to study the role of the calcium-sensing receptor (CaSR) on protein tyrosine phosphorylation in boar spermatozoa under capacitating conditions. To do this, boar spermatozoa were incubated in Tyrode's complete medium for 4 hr and the specific inhibitor of the CaSR, NPS2143, was used. Also, to study the possible mechanism(s) by which this receptor exerts its function, spermatozoa were incubated in the presence of specific inhibitors of the 3-phosphoinositide dependent protein kinase 1 (PDK1) and protein kinase A (PKA). Treatment with NPS2143, GSK2334470, an inhibitor of PDK1 and H-89, an inhibitor of PKA separately induced an increase in tyrosine phosphorylation of 18 and 32 kDa proteins, a decrease in the serine/threonine phosphorylation of the PKA substrates together with a drop in sperm motility and viability. The present work proposes a new signalling pathway of the CaSR, mediated by PDK1 and PKA in boar spermatozoa under capacitating conditions. Our results show that the inhibition of the CaSR induces the inhibition of PDK1 that blocks PKA activity resulting in a rise in tyrosine phosphorylation of p18 and p32 proteins. This novel signalling pathway has not been described before and could be crucial to understand boar sperm capacitation within the female reproductive tract.

Keywords: boar; calcium-sensing receptor; protein kinases; protein tyrosine phosphorylation; spermatozoa.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cyclic AMP-Dependent Protein Kinases / antagonists & inhibitors
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Indazoles / pharmacology
  • Isoquinolines / pharmacology
  • Male
  • Naphthalenes / pharmacology
  • Phenylmethylsulfonyl Fluoride / pharmacology
  • Phosphorylation / drug effects
  • Protein Kinase Inhibitors / pharmacology
  • Pyrimidines / pharmacology
  • Pyruvate Dehydrogenase Acetyl-Transferring Kinase / antagonists & inhibitors
  • Pyruvate Dehydrogenase Acetyl-Transferring Kinase / metabolism*
  • Receptors, Calcium-Sensing / antagonists & inhibitors
  • Receptors, Calcium-Sensing / metabolism*
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Sperm Capacitation / physiology*
  • Sperm Motility / drug effects
  • Spermatozoa / metabolism*
  • Sulfonamides / pharmacology
  • Sus scrofa / metabolism*
  • Tyrosine / metabolism*

Substances

  • GSK 2334470
  • Indazoles
  • Isoquinolines
  • N-(2-hydroxy-3-(2-cyano-3-chlorophenoxy)propyl)-1,1-dimethyl-2-(2-nephthyl)ethylamine
  • Naphthalenes
  • Protein Kinase Inhibitors
  • Pyrimidines
  • Pyruvate Dehydrogenase Acetyl-Transferring Kinase
  • Receptors, Calcium-Sensing
  • Sulfonamides
  • Tyrosine
  • Phenylmethylsulfonyl Fluoride
  • Cyclic AMP-Dependent Protein Kinases
  • N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide