Exposure of mice to environmentally relevant per- and polyfluoroalkyl substances (PFAS) alters the sperm epigenome

Per- and polyfluoroalkyl substances (PFAS) are a large group of persistent synthetic chemicals and ubiquitous environmental contaminants. Mounting evidence demonstrates that PFAS can bioaccumulate and induce adverse health outcomes, including compromising male reproduction. Despite this, the mechanisms by which PFAS elicits these effects remain unclear. Here, we investigate how an environmentally relevant PFAS cocktail impacts the reproductive function of male Swiss CD1 mice. Following twelve weeks of continuous exposure, we collected blood samples for hormone and PFAS quantification and processed reproductive tissues and spermatozoa for histological and functional assessment. PFAS exposure significantly reduced the rate of daily sperm production, likely due to decreased circulating testosterone and dihydrotestosterone. Further, PFAS-exposed spermatozoa displayed marked alterations to their small non-coding RNA profile, which were linked to dysregulation of early-embryonic gene expression. Notably, these changes occured without significant alteration in sperm viability, motility, or the ability to undergo capacitation or support embryonic development. These findings provide new mechanistic insight into how PFAS exposure impacts male reproductive health.

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Publication Details

Journal
Communications Biology
Published
2025-10-28
DOI
https://doi.org/10.1038/s42003-025-08865-4
Citations
3
Primary Topic
Per- and polyfluoroalkyl substances research
Type
article
Field-Weighted Citation Impact
2.58

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article

Exposure of mice to environmentally relevant per- and polyfluoroalkyl substances (PFAS) alters the sperm epigenome

Reena Desai, Colin C. Conine, Simone J. Stanger, Matthew D. Dun et al.
3 citations
Communications Biology
Per- and polyfluoroalkyl substances research
2.58
article

Exposure of mice to environmentally relevant per- and polyfluoroalkyl substances (PFAS) alters the sperm epigenome

Reena Desai, Colin C. Conine, Simone J. Stanger, Matthew D. Dun, Brett D. Turner, Sri Parameswaran, John E. Schjenken, Geoffry N. De Iuliis, Shannon P. Smyth, Anne‐Louise Gannon, Andrew L. Eamens, David J. Handelsman, Ilana R. Bernstein, Natalie A. Trigg, Shaun D. Roman, Mark P. Green, Brett Nixon, Jacinta H. Martin, Amanda L. Anderson, Louis J. Gillespie
article en
3 citations

Abstract

Per- and polyfluoroalkyl substances (PFAS) are a large group of persistent synthetic chemicals and ubiquitous environmental contaminants. Mounting evidence demonstrates that PFAS can bioaccumulate and induce adverse health outcomes, including compromising male reproduction. Despite this, the mechanisms by which PFAS elicits these effects remain unclear. Here, we investigate how an environmentally relevant PFAS cocktail impacts the reproductive function of male Swiss CD1 mice. Following twelve weeks of continuous exposure, we collected blood samples for hormone and PFAS quantification and processed reproductive tissues and spermatozoa for histological and functional assessment. PFAS exposure significantly reduced the rate of daily sperm production, likely due to decreased circulating testosterone and dihydrotestosterone. Further, PFAS-exposed spermatozoa displayed marked alterations to their small non-coding RNA profile, which were linked to dysregulation of early-embryonic gene expression. Notably, these changes occured without significant alteration in sperm viability, motility, or the ability to undergo capacitation or support embryonic development. These findings provide new mechanistic insight into how PFAS exposure impacts male reproductive health.

Communications BiologyVol. 8(1)
University of Technology Sydney (AU), The University of Sydney (AU), New South Wales Department of Health (AU), Children's Hospital of Philadelphia (US), The University of Melbourne (AU), University of the Sunshine Coast (AU), California Institute for Regenerative Medicine (US), Hunter Medical Research Institute (AU), Anzac Research Institute (AU), University of Newcastle Australia (AU)
Australian Government, Hunter Medical Research Institute, Medical Research Council, National Health and Medical Research Council
Openalex Percentile: Top 10%
Per- and polyfluoroalkyl substances research
2.58
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