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Low doses of Bisphenol S affect post-translational modifications of sperm proteins in male mice
H. Řimnáčová, M. Štiavnická, J. Moravec, M. Chemek, Y. Kolinko, O. García-Álvarez, PR. Mouton, AMC. Trejo, T. Fenclová, N. Eretová, P. Hošek, P. Klein, M. Králíčková, J. Petr, J. Nevoral
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články
Grantová podpora
NV18-01-00544
Ministerstvo Zdravotnictví Ceské Republiky
LO1503
Ministerstvo Školství, Mládeže a Tělovýchovy
SW02690
Ministerstvo Školství, Mládeže a Tělovýchovy
CZ.02.1.01/0.0/0.0/16_019/0000787
Ministerstvo Školství, Mládeže a Tělovýchovy
Progress Q39
Univerzita Karlova v Praze
HBM4EU
H2020 European Research Council
NLK
BioMedCentral
od 2003-12-01
BioMedCentral Open Access
od 2003
Directory of Open Access Journals
od 2003
Free Medical Journals
od 2003
PubMed Central
od 2003
Europe PubMed Central
od 2003
ProQuest Central
od 2009-01-01
Open Access Digital Library
od 2003-01-01
Open Access Digital Library
od 2003-01-01
Open Access Digital Library
od 2003-01-01
Medline Complete (EBSCOhost)
od 2003-01-01
Health & Medicine (ProQuest)
od 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2003
Springer Nature OA/Free Journals
od 2003-12-01
- MeSH
- acetylace účinky léků MeSH
- endokrinní disruptory farmakologie MeSH
- epigeneze genetická MeSH
- fenoly farmakologie MeSH
- fosforylace účinky léků MeSH
- myši MeSH
- poškození DNA účinky léků MeSH
- posttranslační úpravy proteinů účinky léků MeSH
- spermie účinky léků MeSH
- sulfony farmakologie MeSH
- testis účinky léků patologie MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- zrání spermie účinky léků MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
BACKGROUND: Bisphenol S (BPS) is increasingly used as a replacement for bisphenol A in the manufacture of products containing polycarbonates and epoxy resins. However, further studies of BPS exposure are needed for the assessment of health risks to humans. In this study we assessed the potential harmfulness of low-dose BPS on reproduction in male mice. METHODS: To simulate human exposure under experimental conditions, 8-week-old outbred ICR male mice received 8 weeks of drinking water containing a broad range of BPS doses [0.001, 1.0, or 100 μg/kg body weight (bw)/day, BPS1-3] or vehicle control. Mice were sacrificed and testicular tissue taken for histological analysis and protein identification by nano-liquid chromatography/mass spectrometry (MS) and sperm collected for immunodetection of acetylated lysine and phosphorylated tyrosine followed by protein characterisation using matrix-assisted laser desorption ionisation time-of-flight MS (MALDI-TOF MS). RESULTS: The results indicate that compared to vehicle, 100 μg/kg/day exposure (BPS3) leads to 1) significant histopathology in testicular tissue; and, 2) higher levels of the histone protein γH2AX, a reliable marker of DNA damage. There were fewer mature spermatozoa in the germ layer in the experimental group treated with 1 μg/kg bw (BPS2). Finally, western blot and MALDI-TOF MS studies showed significant alterations in the sperm acetylome and phosphorylome in mice treated with the lowest exposure (0.001 μg/kg/day; BPS1), although the dose is several times lower than what has been published so far. CONCLUSIONS: In summary, this range of qualitative and quantitative findings in young male mice raise the possibility that very low doses of BPS may impair mammalian reproduction through epigenetic modifications of sperm proteins.
Institute of Animal Science 10 Uhrineves Prague Czech Republic
SRC Biosciences and University of South Florida Tampa FL USA
Citace poskytuje Crossref.org
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