Influence of in vitro capacitation time on structural and functional human sperm parameters

Asian J Androl. 2020 Sep-Oct;22(5):447-453. doi: 10.4103/aja.aja_104_19.

Abstract

A cascade of dramatic physiological events is linked to the sperm acrosome reaction and binding to the oocyte's zona pellucida during human sperm capacitation. However, structural and functional sperm changes during capacitation currently remain poorly defined. Here, we performed a multibiomarker approach based on the utilization of sperm concentration, motility, viability, morphology, acrosome reaction, tyrosine phosphorylation, DNA fragmentation, and lectin-binding sites to analyze the impact caused by swim-up selection times (uncapacitated, 1 h capacitated, and 4 h capacitated) on sperm function and structure in normozoospermic samples. We found that a 4 h swim-up capacitation increased sperm quality, because a large number of cells with normal morphology and lower DNA fragmentation rates were recovered. Furthermore, the long-term capacitation induced a higher percentage of cells with tyrosine phosphorylation of the principal piece as well as a redistribution of lectin-binding sites. Overall, the multivariate biomarkers analyzed showed a less variable distribution on spermatozoa recovered after 4 h capacitation than that with the shorter capacitation time. These findings stress the importance of capacitation time as a relevant factor in sperm quality with potential biological reproductive implications both for basic research and in assisted reproduction techniques.

Keywords: DNA fragmentation; acrosome reaction; capacitation; glycocalyx; lectin-binding sites; membrane integrity; protein phosphorylation; sperm selection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrosome Reaction
  • Biomarkers
  • DNA Fragmentation
  • Humans
  • In Vitro Techniques
  • Lectins / metabolism*
  • Male
  • Phosphorylation
  • Receptors, Cell Surface / metabolism
  • Sperm Capacitation*
  • Sperm Count*
  • Sperm Motility*
  • Spermatozoa / cytology*
  • Spermatozoa / physiology*
  • Time Factors
  • Tyrosine / metabolism

Substances

  • Biomarkers
  • Lectins
  • Receptors, Cell Surface
  • Tyrosine