Expression, cellular localization, and involvement of the pentose phosphate pathway enzymes in the regulation of ram sperm capacitation

Theriogenology. 2016 Aug;86(3):704-14. doi: 10.1016/j.theriogenology.2016.02.024. Epub 2016 Mar 8.

Abstract

Spermatozoa require substantially more ATP than other cells, not only for sustaining sperm motility but also for regulating protein phosphorylation during capacitation. In this study, we have reported for the first time the presence of the two key enzymes of the pentose phosphate pathway (PPP), glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase in ovine spermatozoa by indirect immunofluorescence, Western blotting, in-gel activity, and reverse transcription polymerase chain reaction analysis. We found that the activity of both enzymes significantly increased after in vitro capacitation in the presence of high-cAMP levels, with a concomitant increase in protein tyrosine phosphorylation and in the proportion of sperm-capacitated pattern assessed by the chlortetracycline staining. These results suggest that PPP is related with the progress of capacitation and that a relationship between calcium compartmentalization, protein tyrosine phosphorylation and PPP seems to exist. This is the first report that shows a connection between the PPP, cAMP/PKA signaling pathways and sperm capacitation. These findings can be of high-biological importance to improve our knowledge of the biochemical mechanisms involved in the acquisition of mammalian sperm functional competence and, ultimately, fertility.

Keywords: Chlortetracycline staining; Enzyme expression; Ovine sperm metabolism; Tyrosine phosphorylation.

MeSH terms

  • Animals
  • Gene Expression Regulation / physiology*
  • Glucosephosphate Dehydrogenase / metabolism
  • Hydrogen-Ion Concentration
  • Male
  • Pentose Phosphate Pathway / physiology*
  • Phosphogluconate Dehydrogenase / genetics
  • Phosphogluconate Dehydrogenase / metabolism
  • Protein Transport
  • Sheep / physiology*
  • Sperm Capacitation / physiology*
  • Spermatozoa / physiology*

Substances

  • Phosphogluconate Dehydrogenase
  • Glucosephosphate Dehydrogenase