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Gene expression profiling of changes induced by maternal diabetes in the embryonic heart
R. Bohuslavova, L. Skvorova, R. Cerychova, G. Pavlinkova,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- embryo savčí MeSH
- experimentální diabetes mellitus genetika metabolismus MeSH
- faktor 1 indukovatelný hypoxií - podjednotka alfa metabolismus MeSH
- hypoxie genetika metabolismus MeSH
- inbrední kmeny myší MeSH
- messenger RNA metabolismus MeSH
- myokard metabolismus MeSH
- srdce embryologie MeSH
- stanovení celkové genové exprese MeSH
- těhotenství při diabetu genetika metabolismus MeSH
- těhotenství MeSH
- vaskulární endoteliální růstový faktor A genetika MeSH
- vývojová regulace genové exprese * MeSH
- zvířata MeSH
- Check Tag
- těhotenství MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Cardiovascular defects are one of the most common congenital defects associated with maternal diabetes. Based on whole embryo gene expression microarray analysis, 11 genes were chosen for temporal expression analysis of diabetes-exposed hearts. The majority of the selected genes were deregulated in diabetes-exposed hearts compared to our controls at E13.5, E14.5, and E18.5. We showed increased hypoxia and HIF-1α protein levels in diabetes-exposed hearts at E10.5, which is a critical time point for the induction of developmental defects associated with diabetic embryopathy. Additionally, we found increased cardiac Vegfa levels that might trigger developmental abnormalities associated with diabetic embryopathy. Our results show that maternal diabetes affects the temporal expression pattern of gene encoding molecules involved in heart development and tissue remodelling and that these molecules might affect heart maturation processes and thus, the final outcome of diabetic pregnancies.
Citace poskytuje Crossref.org
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