Reference : The hypoxia-inducible factor HIF-1 promotes intramyocardial expression of VEGF in inf...
Scientific journals : Article
Human health sciences : Pediatrics
http://hdl.handle.net/2268/92677
The hypoxia-inducible factor HIF-1 promotes intramyocardial expression of VEGF in infants with congenital cardiac defects.
English
Qing, Ma [Rheinisch - Westfälische Technische Hochschule Aachen - RWTH > Pediatric Cardiology > > >]
Gorlach, Agnes [Technical University Munich > German Heart Center Munich > Pediatric Cardiology and Congenital Heart Disease > >]
SCHUMACHER, Katharina [Rheinisch - Westfälische Technische Hochschule Aachen - RWTH > Pediatric Cardiology > > >]
Woltje, Michael [Rheinisch - Westfälische Technische Hochschule Aachen - RWTH > Interdisciplinary Center for Clinical Research BIOMAT > > >]
Vazquez-Jimenez, Jamie F [Rheinisch - Westfälische Technische Hochschule Aachen - RWTH > Pediatric Cardiac Surgery > > >]
Hess, John [Technical University Munich > German Heart Center Munich > Pediatric Cardiology and Congenital Heart Disease > >]
SEGHAYE, Marie-Christine mailto [Rheinisch - Westfälische Technische Hochschule Aachen - RWTH > Pediatric Cardiology > > >]
May-2007
Basic Research in Cardiology
Dr Dietrich Steinkopff Verlag
102
3
224-232
Yes (verified by ORBi)
International
0300-8428
Darmstadt
Germany
[en] Blotting, Western ; Cyanosis/genetics ; Female ; Heart Defects, Congenital/genetics/metabolism ; Humans ; Hypoxia-Inducible Factor 1/biosynthesis ; Infant ; Infant, Newborn ; Male ; Myocardium/metabolism/pathology ; Nitric Oxide Synthase/biosynthesis ; Up-Regulation ; Vascular Endothelial Growth Factor A/biosynthesis
[en] OBJECTIVES: The response to hypoxia is primarily mediated by the transcription factor hypoxia-inducible factor-1 (HIF-1) which leads to the induction of a variety of adaptive gene products including vascular endothelial growth factor (VEGF) and endothelial nitric oxide synthase (eNOS). This study was designed to test the hypothesis that HIF-1 and its target genes would be upregulated in the ventricular myocardium of infants with cyanotic congenital cardiac defects. METHODS: 14 infants with cyanotic (n = 7) or acyanotic cardiac defects (n = 7) were investigated. Samples from the right ventricular myocardium taken immediately after aortic clamping were studied for protein expression and DNA-binding activity. RESULTS: Protein levels of HIF-1alpha were significantly elevated in patients with cyanotic compared to acyanotic congenital heart disease and inversely correlated with the degree of hypoxemia. This response was accompanied by significantly enhanced HIF-1 DNA binding activity. Furthermore, protein levels of VEGF and eNOS were significantly higher in the myocardium of cyanotic than of acyanotic infants. To test the potential involvement of upstream regulatory pathways, activation of MAP kinases was determined. Intramyocardial levels of phosphorylated p38 MAP kinase, but not of ERK1/2 were significantly higher in infants with cyanotic compared to those with acyanotic congenital heart disease and inversely correlated to hypoxemia. CONCLUSIONS: These findings show that chronic hypoxemia is associated with the induction and stabilization of the transcription factor HIF-1 as well as its target genes VEGF and eNOS in the myocardium of infants with cyanotic cardiac defects. Thus, stabilization of HIF-1 and induction of the adaptive hypoxia response could particularly participate in myocardial remodeling in children with congenital cardiac defects and chronic hypoxemia.
http://hdl.handle.net/2268/92677
10.1007/s00395-007-0639-2
Epub 2007 Feb 2

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