Sperm Cholesterol Content Modifies Sperm Function and TRPV1-Mediated Sperm Migration

Int J Mol Sci. 2021 Mar 18;22(6):3126. doi: 10.3390/ijms22063126.

Abstract

Transient receptor potential channels-vanilloid receptor 1 (TRPV1) regulates thermotaxis in sperm-oriented motility. We investigated the role of membrane cholesterol (Chol) on TRPV1-mediated human sperm migration. Semen samples were obtained from five normozoospemic healthy volunteers. Sperm membrane Chol content, quantified by liquid chromatography-mass spectrometry, was modified by incubating cells with 2-hydroxypropyl-ß-cyclodextrin (CD) or the complex between CD and Chol (CD:Chol). The effect on sperm migration on a 10 μM capsaicin gradient (CPS), a TRPV1 agonist, was then investigated. Motility parameters were evaluated by Sperm Class Analyser. Intracellular calcium concentration and acrosome reaction were measured by staining with calcium orange and FITC-conjugated anti-CD46 antibody, respectively. TRPV1-Chol interaction was modelled by computational molecular-modelling (MM). CD and CD:Chol, respectively, reduced and increased membrane Chol content in a dose-dependent manner, resulting in a dose-dependent increase and reduction of sperm migration in a CPS gradient. MM confirmed a specific interaction of Chol with a TRPV1 domain that appeared precluded to the Chol epimer epicholesterol (Epi-Chol). Accordingly, CD:Epi-Chol was significantly less efficient than CD:Chol, in reducing sperm migration under CPS gradient. Chol inhibits TRPV1-mediated sperm function by directly interacting with a consensus sequence of the receptor.

Keywords: cholesterol recognition amino acid consensus sequence; epicholesterol; molecular modeling; sperm membrane; thermotaxis.

MeSH terms

  • Adult
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Cholesterol / metabolism*
  • Cyclodextrins / pharmacology
  • Humans
  • Male
  • Models, Molecular
  • Sperm Motility*
  • Spermatozoa / metabolism*
  • TRPV Cation Channels / chemistry
  • TRPV Cation Channels / metabolism*

Substances

  • Cyclodextrins
  • TRPV Cation Channels
  • TRPV1 protein, human
  • Cholesterol