A novel functional estrogen receptor on human sperm membrane interferes with progesterone effects

Mol Cell Endocrinol. 2000 Mar 30;161(1-2):31-5. doi: 10.1016/s0303-7207(99)00220-8.

Abstract

We have identified an estrogen receptor of approximately 29 kDa apparent molecular weight in human sperm membranes by ligand and Western blot analysis, respectively, using peroxidase-conjugated E(2) and an antibody directed against the ligand binding region of the genomic receptor (alphaH222). Such receptor is functional since 17betaE(2) induces a rapid and sustained increase of intracellular calcium concentrations ([Ca(2+)](i)) which is completely eliminated by preincubation with alphaH222. 17betaE(2) effects on calcium are clearly mediated by a membrane receptor, as they are reproduced by the membrane-impermeable conjugate of the hormone BSA-E(2). Dose-response curve for this effect is biphasic with EC(50)s in the nanomolar and micromolar range. In addition to calcium increase, 17betaE(2) stimulates tyrosine phosphorylation of several sperm proteins including the 29-kDa protein band. Preincubation of human sperm with 17betaE(2) inhibits calcium and acrosome reaction increases in response to progesterone. We conclude that estrogens may play a role in the modulation of non-genomic action of progesterone (P) in human sperm during the process of fertilization.

MeSH terms

  • Acrosome Reaction / drug effects
  • Calcium Signaling / drug effects
  • Cell Membrane / chemistry
  • Cell Membrane / drug effects
  • Dose-Response Relationship, Drug
  • Estradiol / pharmacology
  • Humans
  • Male
  • Membrane Proteins / metabolism
  • Phosphorylation / drug effects
  • Progesterone / antagonists & inhibitors*
  • Progesterone / pharmacology
  • Receptors, Estrogen / chemistry
  • Receptors, Estrogen / metabolism*
  • Spermatozoa / chemistry*
  • Spermatozoa / drug effects
  • Spermatozoa / ultrastructure
  • Tyrosine / drug effects
  • Tyrosine / metabolism

Substances

  • Membrane Proteins
  • Receptors, Estrogen
  • Tyrosine
  • Progesterone
  • Estradiol