Comparative proteomics reveals the underlying toxicological mechanism of low sperm motility induced by iron ion radiation in mice

Reprod Toxicol. 2016 Oct:65:148-158. doi: 10.1016/j.reprotox.2016.07.014. Epub 2016 Jul 25.

Abstract

The toxicological mechanism of low sperm motility induced by iron ion radiation (IIR) was investigated in mice. Reproductive organ indices were measured following whole-body irradiation with a 2Gy iron ion beam. Two-dimensional gel electrophoresis, immunoblotting and immunofluorescence were used to analyze protein expression, and real-time polymerase chain reaction was performed to confirm altered gene expression. Reproductive organ indices and sperm motility were lowest 2 weeks after IIR. Sperm function changes via testis and cauda epididymis function were also determined at this time point. Sixteen differentially expressed proteins were identified in sperm 2 weeks after IIR. Bioinformatics analysis indicated that alpha-enolase (Eno1) may be important in the regulation of glycolysis in sperm, and Eno1 expression was correlated with sperm motility. Eno1 may be a potential marker for low sperm motility induced by IIR, and these results may provide a useful reference for changes in astronaut fertility during long space missions.

Keywords: Motility; Proteomics; Space radiation; Sperm.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Heavy Ions / adverse effects*
  • Iron / toxicity*
  • Male
  • Mice
  • Phosphopyruvate Hydratase / metabolism
  • Proteomics
  • Radiation Injuries, Experimental / metabolism*
  • Sperm Count
  • Sperm Motility*
  • Spermatozoa / metabolism*
  • Whole-Body Irradiation

Substances

  • Iron
  • Eno1 protein, mouse
  • Phosphopyruvate Hydratase