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Inhibition of the mouse sperm surface alpha-D-mannosidase inhibits sperm-egg binding in vitro

G A Cornwall1, D R Tulsiani, M C Orgebin-Crist

  • 1Department of Obstetrics and Gynecology Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2633.

Insights

Sperm alpha-D-mannosidase plays a key role in fertilization by mediating sperm-egg binding. Inhibiting this enzyme with specific sugars significantly reduces binding without harming sperm motility or acrosome integrity.

Area of Science:

  • Reproductive Biology
  • Enzymology
  • Cell Biology

Background:

  • A novel alpha-D-mannosidase has been identified on the surface of various mammalian spermatozoa, including human.
  • Mannosyl residues on the egg zona pellucida are hypothesized to be crucial for sperm-egg binding.

Purpose of the Study:

  • To investigate the role of sperm alpha-D-mannosidase in the fertilization process.
  • To determine if inhibiting sperm alpha-D-mannosidase affects sperm-egg binding.

Main Methods:

  • Mouse spermatozoa were incubated with various sugars (alpha-methyl mannoside, D-mannose, etc.) and nucleotide sugars.
  • Sperm-egg binding, sperm motility, and acrosome integrity were assessed.
  • The effect of a mannose-containing oligosaccharide on sperm-egg binding and enzyme activity was evaluated.

Main Results:

  • Inhibitory sugars and D-mannose caused a dose-dependent decrease in sperm-egg binding, correlating with reduced mannosidase activity.
  • Galactose had no effect on binding or enzyme activity.
  • A mannose-containing oligosaccharide significantly reduced sperm-egg binding and inhibited mannosidase activity without affecting sperm motility or acrosome.

Conclusions:

  • Sperm alpha-D-mannosidase is implicated in mediating sperm-egg binding during fertilization.
  • The enzyme's activity is crucial for successful sperm-egg interaction.

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