It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
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.
Changes in semen quality over the last 50 years correspond with increasing environmental stressors. Here, Moon et al. causally identified stress-mediated changes in secreted extracellular vesicles as regulators of sperm motility in mice and men.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details



1 University of Colorado Anschutz Medical Campus School of Medicine, Department of Psychiatry, Aurora, USA (GRID:grid.430503.1) (ISNI:0000 0001 0703 675X); University of Maryland Baltimore, Department of Pharmacology, Baltimore, USA (GRID:grid.411024.2) (ISNI:0000 0001 2175 4264)
2 University of Maryland Baltimore, Department of Pharmacology, Baltimore, USA (GRID:grid.411024.2) (ISNI:0000 0001 2175 4264)
3 University of Colorado Anschutz Medical Campus School of Medicine, Department of Psychiatry, Aurora, USA (GRID:grid.430503.1) (ISNI:0000 0001 0703 675X)
4 University of Colorado Anschutz Medical Campus, Department of Biostatistics and Informatics, Colorado School of Public Health, Aurora, USA (GRID:grid.430503.1) (ISNI:0000 0001 0703 675X)
5 University of Maryland Baltimore, Department of Physiology, Baltimore, USA (GRID:grid.411024.2) (ISNI:0000 0001 2175 4264)