BAS/BSCR31 Metabolic homoeostasis is maintained in myocardial hibernation by adaptive changes in the transcriptome and proteome. Issue 17 (26th August 2010)
- Record Type:
- Journal Article
- Title:
- BAS/BSCR31 Metabolic homoeostasis is maintained in myocardial hibernation by adaptive changes in the transcriptome and proteome. Issue 17 (26th August 2010)
- Main Title:
- BAS/BSCR31 Metabolic homoeostasis is maintained in myocardial hibernation by adaptive changes in the transcriptome and proteome
- Authors:
- Zampetaki, Anna
May, D
Oren, G
Yin, X
Xu, Q
Horrevoets, A
Keshet, E
Mayr, M - Abstract:
- Abstract : Rationale: We have recently established a transgenic mouse model for conditional induction of long-term hibernation via myocardium-specific induction of a VEGF-sequestering soluble receptor. Objective: Using a combined '-omics' approach, we aim to resolve the cardioprotective response that preserves myocardial viability under chronic hypoxia by integrating mRNA, protein and metabolite changes in unsupervised network analysis. Methods and results: A genome array, difference in gel electrophoresis and proton nuclear magnetic resonance spectroscopy were employed to dissect the hibernation process into an initiation and a maintenance phase. The initiation phase was characterised by peak levels of K(ATP) channel and glucose transporter 1 (GLUT1) expression. Glibenclamide, an inhibitor of K(ATP) channels, blocked GLUT1 induction. In the maintenance phase, tissue hypoxia and GLUT1 expression were reduced and metabolite concentrations were kept relatively constant. Unguided bioinformatics analysis on the combined datasets confirmed that anaerobic glycolysis was affected and that the observed enzymatic changes in cardiac metabolism were directly linked to hypoxia-inducible factor (HIF)-1 activation. Notably, the combination of the proteomic and transcriptomic datasets improved the statistical confidence of the pathway analysis by two orders of magnitude, with HIF–hypoxia–Akt signalling and glycolysis being the most significant. Conclusions: We demonstrate how combiningAbstract : Rationale: We have recently established a transgenic mouse model for conditional induction of long-term hibernation via myocardium-specific induction of a VEGF-sequestering soluble receptor. Objective: Using a combined '-omics' approach, we aim to resolve the cardioprotective response that preserves myocardial viability under chronic hypoxia by integrating mRNA, protein and metabolite changes in unsupervised network analysis. Methods and results: A genome array, difference in gel electrophoresis and proton nuclear magnetic resonance spectroscopy were employed to dissect the hibernation process into an initiation and a maintenance phase. The initiation phase was characterised by peak levels of K(ATP) channel and glucose transporter 1 (GLUT1) expression. Glibenclamide, an inhibitor of K(ATP) channels, blocked GLUT1 induction. In the maintenance phase, tissue hypoxia and GLUT1 expression were reduced and metabolite concentrations were kept relatively constant. Unguided bioinformatics analysis on the combined datasets confirmed that anaerobic glycolysis was affected and that the observed enzymatic changes in cardiac metabolism were directly linked to hypoxia-inducible factor (HIF)-1 activation. Notably, the combination of the proteomic and transcriptomic datasets improved the statistical confidence of the pathway analysis by two orders of magnitude, with HIF–hypoxia–Akt signalling and glycolysis being the most significant. Conclusions: We demonstrate how combining different '-omics' datasets aids in the identification of key biological pathways: chronic hypoxia resulted in a pronounced adaptive response at the transcript and the protein level to keep metabolite levels steady. This preservation of metabolic homoeostasis is likely to contribute to the long-term survival of the hibernating myocardium. … (more)
- Is Part Of:
- Heart. Volume 96:Issue 17(2010)
- Journal:
- Heart
- Issue:
- Volume 96:Issue 17(2010)
- Issue Display:
- Volume 96, Issue 17 (2010)
- Year:
- 2010
- Volume:
- 96
- Issue:
- 17
- Issue Sort Value:
- 2010-0096-0017-0000
- Page Start:
- e21
- Page End:
- e21
- Publication Date:
- 2010-08-26
- Subjects:
- Heart -- Diseases -- Treatment -- Periodicals
Cardiology -- Periodicals
616.12 - Journal URLs:
- http://www.bmj.com/archive ↗
http://heart.bmj.com ↗
http://www.heartjnl.com ↗ - DOI:
- 10.1136/hrt.2010.205781.42 ↗
- Languages:
- English
- ISSNs:
- 1355-6037
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 18054.xml