The Ubiquitin-Proteasome System Participates in Sperm Surface Subproteome Remodeling during Boar Sperm Capacitation

Biomolecules. 2023 Jun 15;13(6):996. doi: 10.3390/biom13060996.

Abstract

Sperm capacitation is a complex process endowing biological and biochemical changes to a spermatozoon for a successful encounter with an oocyte. The present study focused on the role of the ubiquitin-proteasome system (UPS) in the remodeling of the sperm surface subproteome. The sperm surface subproteome from non-capacitated and in vitro capacitated (IVC) porcine spermatozoa, with and without proteasomal inhibition, was selectively isolated. The purified sperm surface subproteome was analyzed using high-resolution, quantitative liquid chromatography-mass spectrometry (LC-MS) in four replicates. We identified 1680 HUGO annotated proteins, out of which we found 91 to be at least 1.5× less abundant (p < 0.05) and 141 to be at least 1.5× more abundant (p < 0.05) on the surface of IVC spermatozoa. These proteins were associated with sperm capacitation, hyperactivation, metabolism, acrosomal exocytosis, and fertilization. Abundances of 14 proteins were found to be significantly different (p < 0.05), exceeding a 1.5-fold abundance between the proteasomally inhibited (100 µM MG132) and vehicle control (0.2% ethanol) groups. The proteins NIF3L1, CSE1L, NDUFB7, PGLS, PPP4C, STK39, and TPRG1L were found to be more abundant; while BPHL, GSN, GSPT1, PFDN4, STYXL1, TIMM10, and UBXN4 were found to be less abundant in proteasomally inhibited IVC spermatozoa. Despite the UPS having a narrow range of targets, it modulated sperm metabolism and binding by regulating susceptible surface proteins. Changes in CSE1L, PFDN4, and STK39 during in vitro capacitation were confirmed using immunocytochemistry, image-based flow cytometry, and Western blotting. The results confirmed the active participation of the UPS in the extensive sperm surface proteome remodeling that occurs during boar sperm capacitation. This work will help us to identify new pharmacological mechanisms to positively or negatively modulate sperm fertilizing ability in food animals and humans.

Keywords: CSE1L; PFDN4; STK39/SPAK; pig; sperm capacitation; sperm surface protein; spermatozoon; ubiquitin–proteasome system.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Humans
  • Male
  • Membrane Proteins / metabolism
  • Proteasome Endopeptidase Complex* / metabolism
  • Semen / metabolism
  • Sperm Capacitation* / physiology
  • Spermatozoa / metabolism
  • Swine
  • Ubiquitin / metabolism

Substances

  • Proteasome Endopeptidase Complex
  • Ubiquitin
  • UBXN4 protein, human
  • Membrane Proteins

Grants and funding

This research was funded by the USDA National Institute of Food and Agriculture, Agriculture and Food Research Initiative Competitive Grants (grants nos. 2020-67015-31017 (P.S.), 2021-67015-33404 (P.S.), 2022-67015-36298 (K.K.)); the University of Missouri CAFNR Joy of Discovery Seed Grant award (P.S., M.Z.); and seed funding from the College of Agriculture, Food and Natural Resources (CAFNR), University of Missouri (PS).