SPINK3 modulates mouse sperm physiology through the reduction of nitric oxide level independently of its trypsin inhibitory activity

Reproduction. 2012 Mar;143(3):281-95. doi: 10.1530/REP-11-0107. Epub 2012 Jan 6.

Abstract

Serine protease inhibitor Kazal-type (SPINK3)/P12/PSTI-II is a small secretory protein from mouse seminal vesicle which contains a KAZAL domain and shows calcium (Ca(2+))-transport inhibitory (caltrin) activity. This molecule was obtained as a recombinant protein and its effect on capacitated sperm cells was examined. SPINK3 inhibited trypsin activity in vitro while the fusion protein GST-SPINK3 had no effect on this enzyme activity. The inactive GST-SPINK3 significantly reduced the percentage of spermatozoa positively stained for nitric oxide (NO) with the specific probe DAF-FM DA and NO concentration measured by Griess method in capacitated mouse sperm; the same effect was observed when sperm were capacitated under low Ca(2+) concentration, using either intracellular (BAPTA-AM) or extracellular Ca(2+) (EDTA) chelators. The percentage of sperm showing spontaneous and progesterone-induced acrosomal reaction was significantly lower in the presence of GST-SPINK3 compared to untreated capacitated spermatozoa. Interestingly, this decrease was overcome by the exogenous addition of the NO donors, sodium nitroprusside (SNP), and S-nitrosoglutathione (GSNO). Phosphorylation of sperm proteins in tyrosine residues was partially affected by GST-SPINK3, however, only GSNO was able to reverse this effect. Sperm progressive motility was not significantly diminished by GST-SPINK3 or BAPTA-AM but enhanced by the addition of SNP. This is the first report that demonstrates that SPINK3 modulates sperm physiology through a downstream reduction of endogenous NO concentration and independently of SPINK3 trypsin inhibitory activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Survival / drug effects
  • Down-Regulation / drug effects
  • Enzyme Inhibitors / metabolism
  • Enzyme Inhibitors / pharmacology
  • Glycoproteins / genetics
  • Glycoproteins / pharmacology
  • Glycoproteins / physiology*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Models, Biological
  • Nitric Oxide / analysis
  • Nitric Oxide / metabolism*
  • Osmolar Concentration
  • Prostatic Secretory Proteins / genetics
  • Prostatic Secretory Proteins / pharmacology
  • Prostatic Secretory Proteins / physiology*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / pharmacology
  • Semen Analysis
  • Sperm Capacitation / drug effects
  • Sperm Capacitation / physiology
  • Spermatozoa / drug effects
  • Spermatozoa / metabolism
  • Spermatozoa / physiology*
  • Trypsin / metabolism
  • Trypsin / pharmacology
  • Trypsin Inhibitor, Kazal Pancreatic

Substances

  • Enzyme Inhibitors
  • Glycoproteins
  • Prostatic Secretory Proteins
  • Recombinant Fusion Proteins
  • Spink1 protein, mouse
  • Nitric Oxide
  • Trypsin Inhibitor, Kazal Pancreatic
  • Trypsin