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Stress increases sperm respiration and motility in mice and men

Author

Listed:
  • Nickole Moon

    (University of Colorado Anschutz Medical Campus School of Medicine
    University of Maryland Baltimore)

  • Christopher P. Morgan

    (University of Maryland Baltimore)

  • Ruth Marx-Rattner

    (University of Maryland Baltimore)

  • Alyssa Jeng

    (University of Colorado Anschutz Medical Campus School of Medicine)

  • Rachel L. Johnson

    (University of Colorado Anschutz Medical Campus)

  • Ijeoma Chikezie

    (University of Maryland Baltimore)

  • Carmen Mannella

    (University of Maryland Baltimore)

  • Mary D. Sammel

    (University of Colorado Anschutz Medical Campus)

  • C. Neill Epperson

    (University of Colorado Anschutz Medical Campus School of Medicine)

  • Tracy L. Bale

    (University of Colorado Anschutz Medical Campus School of Medicine
    University of Maryland Baltimore)

Abstract

Semen quality and fertility has declined over the last 50 years, corresponding to ever-increasing environmental stressors. However, the cellular mechanisms involved and their impact on sperm functions remain unknown. In a repeated sampling human cohort study, we identify a significant effect of prior perceived stress to increase sperm motility 2-3 months following stress, timing that expands upon our previous studies revealing significant stress-associated changes in sperm RNA important for fertility. We mechanistically examine this post-stress timing in mice using an in vitro stress model in the epididymal epithelial cells responsible for sperm maturation and find 7282 differentially H3K27me3 bound DNA regions involving genes critical for mitochondrial and metabolic pathways. Further, prior stress exposure significantly changes the composition and size of epithelial cell-secreted extracellular vesicles that when incubated with mouse sperm, increase mitochondrial respiration and sperm motility, adding to our prior work showing impacts on embryo development. Together, these studies identify a time-dependent, translational signaling pathway that communicates stress experience to sperm, ultimately affecting reproductive functions.

Suggested Citation

  • Nickole Moon & Christopher P. Morgan & Ruth Marx-Rattner & Alyssa Jeng & Rachel L. Johnson & Ijeoma Chikezie & Carmen Mannella & Mary D. Sammel & C. Neill Epperson & Tracy L. Bale, 2024. "Stress increases sperm respiration and motility in mice and men," Nature Communications, Nature, vol. 15(1), pages 1-20, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-52319-0
    DOI: 10.1038/s41467-024-52319-0
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    References listed on IDEAS

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