Adverse effects of Hif1a mutation and maternal diabetes on the offspring heart
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
16-06825S
Grantová Agentura České Republiky - International
228416
Grantová Agentura, Univerzita Karlova - International
PubMed
29753320
PubMed Central
PMC5948854
DOI
10.1186/s12933-018-0713-0
PII: 10.1186/s12933-018-0713-0
Knihovny.cz E-zdroje
- Klíčová slova
- Echocardiography, Fetal programming, Heart remodelling, Hif1a haploinsufficiency, Maternal diabetes,
- MeSH
- experimentální diabetes mellitus komplikace metabolismus patologie MeSH
- faktor 1 indukovatelný hypoxií - podjednotka alfa genetika metabolismus MeSH
- funkce levé komory srdeční MeSH
- gestační diabetes * metabolismus patologie MeSH
- haploinsuficience MeSH
- interakce genů a prostředí MeSH
- kardiovaskulární nemoci genetika metabolismus patologie patofyziologie MeSH
- mutace * MeSH
- myokard metabolismus patologie MeSH
- myši knockoutované MeSH
- remodelace komor MeSH
- rizikové faktory MeSH
- těhotenství MeSH
- vývojová regulace genové exprese MeSH
- zpožděný efekt prenatální expozice * MeSH
- zvířata MeSH
- Check Tag
- těhotenství MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- faktor 1 indukovatelný hypoxií - podjednotka alfa MeSH
- Hif1a protein, mouse MeSH Prohlížeč
BACKGROUND: Epidemiological studies show that maternal diabetes predisposes offspring to cardiovascular and metabolic disorders. However, the precise mechanisms for the underlying penetrance and disease predisposition remain poorly understood. We examined whether hypoxia-inducible factor 1 alpha, in combination with exposure to a diabetic intrauterine environment, influences the function and molecular structure of the adult offspring heart. METHODS AND RESULTS: In a mouse model, we demonstrated that haploinsufficient (Hif1a+/-) offspring from a diabetic pregnancy developed left ventricle dysfunction at 12 weeks of age, as manifested by decreased fractional shortening and structural remodeling of the myocardium. Transcriptional profiling by RNA-seq revealed significant transcriptome changes in the left ventricle of diabetes-exposed Hif1a+/- offspring associated with development, metabolism, apoptosis, and blood vessel physiology. In contrast, both wild type and Hif1a+/- offspring from diabetic pregnancies showed changes in immune system processes and inflammatory responses. Immunohistochemical analyses demonstrated that the combination of haploinsufficiency of Hif1a and exposure to maternal diabetes resulted in impaired macrophage infiltration, increased levels of advanced glycation end products, and changes in vascular homeostasis in the adult offspring heart. CONCLUSIONS: Together our findings provide evidence that a global reduction in Hif1a gene dosage increases predisposition of the offspring exposed to maternal diabetes to cardiac dysfunction, and also underscore Hif1a as a critical factor in the fetal programming of adult cardiovascular disease.
EMBL Genomics Core Facility Meyerhofstr 1 69117 Heidelberg Germany
Faculty of Science Charles University Prague Czechia
Institute of Anatomy 1st Faculty of Medicine Charles University Prague Czechia
Institute of Physiology CAS Prague Czechia
Laboratory of Gene Expression Institute of Biotechnology CAS BIOCEV Vestec Czechia
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