In vitro ageing of pig oocytes: effects of the histone deacetylase inhibitor trichostatin A
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
18405435
DOI
10.1017/s0967199408004668
PII: S0967199408004668
Knihovny.cz E-zdroje
- MeSH
- histondeacetylasy metabolismus MeSH
- inhibitory enzymů farmakologie MeSH
- inhibitory histondeacetylas * MeSH
- inhibitory syntézy proteinů farmakologie MeSH
- ionofory farmakologie MeSH
- kultivované buňky MeSH
- kyseliny hydroxamové farmakologie MeSH
- oocyty enzymologie fyziologie MeSH
- prasata fyziologie MeSH
- stárnutí buněk MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- histondeacetylasy MeSH
- inhibitory enzymů MeSH
- inhibitory histondeacetylas * MeSH
- inhibitory syntézy proteinů MeSH
- ionofory MeSH
- kyseliny hydroxamové MeSH
- trichostatin A MeSH Prohlížeč
After in vitro maturation, the unfertilized pig oocytes underwent the process called ageing. This process involves typical events such as fragmentation, spontaneous parthenogenetic activation or lysis. Inhibition of histone deacetylase, using its specific inhibitor trichostatin A (TSA), significantly delayed the maturation of pig oocytes cultured in vitro. The ageing of oocytes matured under the effect of TSA is the same as the ageing in oocytes matured without TSA. The inhibition of histone deacetylase during oocyte ageing significantly reduced the percentage of fragmented oocytes (from 30% in untreated oocytes to 9% in oocytes aged under the effect of 100 nM of TSA). Oocytes matured in vitro and subsequently aged for 1 day under the effects of TSA retained their developmental capacity. After parthenogenetic activation, a significantly higher portion (27% vs. 15%) of oocytes developed to the blastocyst stage after 24 h ageing under 100 nM TSA when compared with oocytes activated after 24 h ageing in a TSA-free medium. The parthenogenetic development in oocytes aged under TSA treatment is similar to the development of fresh oocytes (29% of blastocyst) artificially activated immediately after in vitro maturation.
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