Expression of a2 vacuolar ATPase in spermatozoa is associated with semen quality and chemokine-cytokine profiles in infertile men

PLoS One. 2013 Jul 30;8(7):e70470. doi: 10.1371/journal.pone.0070470. Print 2013.

Abstract

Background: A number of laboratory tests have been developed to determine properties of spermatozoa quality but few have been adopted into routine clinical use in place of the WHO semen analysis. We investigated whether Atp6v0a2 (a2 isoform of vacuolar ATPase) is associated with abnormal semen quality and changes in chemokine-cytokine profiles in infertile men.

Patients and methods: Semen samples were collected from 35 healthy donors and 35 infertile men at the Andrology laboratory from August 2011 to June 2012. The levels of Atp6v0a2 mRNA and protein, and its localization in spermatozoa were determined. a2NTD (the N-terminal portion of Atp6v0a2) and secreted chemokine-cytokine profiles in seminal fluid were measured.

Results: Atp6v0a2 protein (P<0.05) and mRNA (P<0.05) in spermatozoa from infertile men were significantly lower than those from fertile men. Fluorescent microscopy revealed that Atp6v0a2 is mainly expressed in the acrosomal region. Infertile men's seminal fluid had significantly lower G-CSF (P<0.01), GM-CSF (P<0.01), MCP-1 (P<0.05), MIP-1α (P<0.01) and TGF-β1 (P<0.01) levels when compared to the seminal fluid from fertile men. Seminal fluid a2NTD levels were significantly correlated with G-CSF (P<0.01), GM-CSF (P<0.01), MCP-1 (P<0.05), MIP-1α (P<0.01) and TGF-β1 (P<0.01) which are key molecules during the onset of pregnancy.

Conclusion: These results suggested that a critical level of Atp6v0a2 is required for the fertile spermatozoa and its decreased level in spermatozoa could be used to predict male infertility. This study provides a possibility that Atp6v0a2 could be potentially used as a diagnostic marker for the evaluation of male infertility.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Case-Control Studies
  • Chemokines / metabolism
  • Cytokines / metabolism*
  • Gene Expression*
  • Humans
  • Infertility, Male / genetics*
  • Infertility, Male / metabolism*
  • Male
  • Protein Transport
  • Proton-Translocating ATPases / genetics*
  • Proton-Translocating ATPases / metabolism
  • Semen / chemistry*
  • Semen Analysis
  • Sperm Motility
  • Spermatozoa / metabolism*

Substances

  • ATP6V0A2 protein, human
  • Chemokines
  • Cytokines
  • Proton-Translocating ATPases

Grants and funding

The authors thank the Clinical Laboratory, Rosalind Franklin University of Medical and Science, North Chicago, IL for the grant support. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.