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Mechanistic target of rapamycin (mTOR) pathway in Sertoli cells regulates age-dependent changes in sperm DNA methylation.
- Source :
-
ELife [Elife] 2024 Sep 16; Vol. 13. Date of Electronic Publication: 2024 Sep 16. - Publication Year :
- 2024
-
Abstract
- Over the past several decades, a trend toward delayed childbirth has led to increases in parental age at the time of conception. Sperm epigenome undergoes age-dependent changes increasing risks of adverse conditions in offspring conceived by fathers of advanced age. The mechanism(s) linking paternal age with epigenetic changes in sperm remain unknown. The sperm epigenome is shaped in a compartment protected by the blood-testes barrier (BTB) known to deteriorate with age. Permeability of the BTB is regulated by the balance of two mTOR complexes in Sertoli cells where mTOR complex 1 (mTORC1) promotes the opening of the BTB and mTOR complex 2 (mTORC2) promotes its integrity. We hypothesized that this balance is also responsible for age-dependent changes in the sperm epigenome. To test this hypothesis, we analyzed reproductive outcomes, including sperm DNA methylation in transgenic mice with Sertoli cell-specific suppression of mTORC1 ( Rptor KO) or mTORC2 ( Rictor KO). mTORC2 suppression accelerated aging of the sperm DNA methylome and resulted in a reproductive phenotype concordant with older age, including decreased testes weight and sperm counts, and increased percent of morphologically abnormal spermatozoa and mitochondrial DNA copy number. Suppression of mTORC1 resulted in the shift of DNA methylome in sperm opposite to the shift associated with physiological aging - sperm DNA methylome rejuvenation and mild changes in sperm parameters. These results demonstrate for the first time that the balance of mTOR complexes in Sertoli cells regulates the rate of sperm epigenetic aging. Thus, mTOR pathway in Sertoli cells may be used as a novel target of therapeutic interventions to rejuvenate the sperm epigenome in advanced-age fathers.<br />Competing Interests: SA, OA, EM, JM, OO, OS, JP No competing interests declared, AS Reports a relationship with ReGENE LLC that includes board membership, equity or stocks, and funding grants<br /> (© 2024, Amir, Arowolo et al.)
- Subjects :
- Male
Animals
Mice
Mechanistic Target of Rapamycin Complex 1 metabolism
Mechanistic Target of Rapamycin Complex 1 genetics
TOR Serine-Threonine Kinases metabolism
Mice, Knockout
Mechanistic Target of Rapamycin Complex 2 metabolism
Mechanistic Target of Rapamycin Complex 2 genetics
Regulatory-Associated Protein of mTOR metabolism
Regulatory-Associated Protein of mTOR genetics
Mice, Transgenic
Aging physiology
Aging genetics
Signal Transduction
Rapamycin-Insensitive Companion of mTOR Protein metabolism
Rapamycin-Insensitive Companion of mTOR Protein genetics
Epigenesis, Genetic
Sertoli Cells metabolism
DNA Methylation
Spermatozoa metabolism
Spermatozoa physiology
Subjects
Details
- Language :
- English
- ISSN :
- 2050-084X
- Volume :
- 13
- Database :
- MEDLINE
- Journal :
- ELife
- Publication Type :
- Academic Journal
- Accession number :
- 39283662
- Full Text :
- https://doi.org/10.7554/eLife.90992