Počet záznamů: 1  

Partial HIF-1a Deficiency Increases Risk of Diabetic Embryopathy

  1. 1.
    SYSNO ASEP0379011
    Druh ASEPA - Abstrakt
    Zařazení RIVZáznam nebyl označen do RIV
    Zařazení RIVNení vybrán druh dokumentu
    NázevPartial HIF-1a Deficiency Increases Risk of Diabetic Embryopathy
    Tvůrce(i) Pavlínková, Gabriela (BTO-N) RID, ORCID
    Bohuslavová, Romana (BTO-N) RID
    Sedmera, David (FGU-C) RID, ORCID, SAI
    Škvorová, Lada (BTO-N)
    Zdroj.dok.Birth Defects Research Part A-Clinical and Molecular Teratology - ISSN 1542-0752
    Roč. 94, č. 5 (2012), s. 319-319
    Poč.str.1 s.
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slovadiabetic embryopathy ; cardiovascular defects ; transcriptional regulation
    Vědní obor RIVFB - Endokrinologie, diabetologie, metabolizmus, výživa
    CEPGA301/09/0117 GA ČR - Grantová agentura ČR
    CEZAV0Z50520701 - BTO-N (2007-2013)
    AnotaceDiabetic pregnancy is associated with a 4- to 10-fold increased incidence of congenital malformations compared with non-diabetic pregnancy. Diabetic embryopathy can affect any developing organ system, although cardiovascular malformations are most common. Although teratogenic effects of maternal diabetes are well documented, the causes remain elusive. Based on our findings that the embryonic expression of Hif1a is dysregulated by maternal diabetes, and the knowledge that Hif1a-/- embryos have major defects in cardiovascular development, we hypothesized that maternal diabetes impairs HIF-1-controlled hypoxia-response pathways and that these pathways are critically involved in the susceptibility to heart defects observed in diabetic embryopathy. We tested this hypothesis in a genetic mouse model of partial HIF-1deficiency by exposing Hif1a+/- embryos to maternal diabetes. We observed a decreased number of embryos per litter and increased incidence of heart malformations, including atrioventricular septal defects and reduced myocardial mass, in diabetes-exposed Hif1a+/- embryos as compared to Wt embryos. We also detected significant differences in expression of mRNAs in diabetes-exposed Hif1a+/- and Wt embryonic hearts, including those encoded by Vegfa, Flt1, and Cited2. Our data strongly suggest that HIF1-regulated pathways could be one of the key molecular pathways involved in the pathogenesis of the teratogenic insult of maternal diabetes.
    PracovištěBiotechnologický ústav
    KontaktMonika Kopřivová, Monika.Koprivova@ibt.cas.cz, Tel.: 325 873 700
    Rok sběru2013
Počet záznamů: 1  

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