Protease activated receptor 2 and epidermal growth factor receptor are involved in the regulation of human sperm motility

Asian J Androl. 2007 Sep;9(5):690-6. doi: 10.1111/j.1745-7262.2007.00289.x.

Abstract

Aim: To investigate mechanisms of tryptase-induced reduction of sperm motility and explore whether epidermal growth factor receptor (EGF-R) and protease activated receptor 2 (PAR-2)- associated pathways are involved.

Methods: Fresh semen was collected from healthy donors (n = 15). Semen parameters and quality were assessed in accordance with the World Health Organization (WHO) criteria. Swim-up sperm were fixed and subjected to immunocytochemistry and immunoelectronmicroscopy with specific antibodies directed against PAR-2 and EGF-R. Protein extractions from swim-up spermatozoa were analyzed by Western blotting with antibodies for both receptors. Motility of spermatozoa was evaluated by computer-assisted semen analysis.

Results: Immunocytochemistry found PAR-2 and EGF-R in approximately 30% of examined human ejaculated spermatozoa. Both receptors were localized in the plasma membrane. Like tryptase, the PAR-2 synthetic agonist SLIGKV reduced sperm motility, and this effect was inhibited by application of two specific EGF-R pathway blockers (AG1478 and PD168393).

Conclusion: The observed reduction of sperm motility by tryptase through the PAR-2 receptor involves EGF-R pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ejaculation
  • Enzyme Inhibitors / pharmacology
  • ErbB Receptors / antagonists & inhibitors
  • ErbB Receptors / drug effects
  • ErbB Receptors / physiology*
  • Humans
  • Male
  • Microscopy, Immunoelectron
  • Oligopeptides / pharmacology
  • Quinazolines / pharmacology
  • Receptor, PAR-2 / physiology*
  • Reference Values
  • Semen / physiology*
  • Sperm Motility / drug effects
  • Sperm Motility / physiology*
  • Spermatozoa / drug effects
  • Spermatozoa / physiology
  • Spermatozoa / ultrastructure
  • Tyrphostins / pharmacology

Substances

  • Enzyme Inhibitors
  • Oligopeptides
  • PD168393
  • Quinazolines
  • Receptor, PAR-2
  • Tyrphostins
  • seryl-leucyl-isoleucyl--glycyl-lysyl-valine
  • RTKI cpd
  • ErbB Receptors