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Arteriogenic Therapy by Intramyocardial Sustained Delivery of a Novel Growth Factor Combination Prevents Chronic Heart Failure
- Source :
- Circulation, Circulation, American Heart Association, 2011, 124 (9), pp.1059-1069. ⟨10.1161/CIRCULATIONAHA.110.010264⟩, Circulation, 2011, 124 (9), pp.1059-1069. ⟨10.1161/CIRCULATIONAHA.110.010264⟩
- Publication Year :
- 2011
- Publisher :
- HAL CCSD, 2011.
-
Abstract
- Background— Therapeutic angiogenesis is a promising approach for the treatment of cardiovascular diseases, including myocardial infarction and chronic heart failure. We aimed to improve proangiogenic therapies by identifying novel arteriogenic growth factor combinations, developing injectable delivery systems for spatiotemporally controlled growth factor release, and evaluating functional consequences of targeted intramyocardial growth factor delivery in chronic heart failure. Methods and Results— First, we observed that fibroblast growth factor and hepatocyte growth factor synergistically stimulate vascular cell migration and proliferation in vitro. Using 2 in vivo angiogenesis assays (n=5 mice per group), we found that the growth factor combination results in a more potent and durable angiogenic response than either growth factor used alone. Furthermore, we determined that the molecular mechanisms involve potentiation of Akt and mitogen-activated protein kinase signal transduction pathways, as well as upregulation of angiogenic growth factor receptors. Next, we developed crosslinked albumin-alginate microcapsules that sequentially release fibroblast growth factor-2 and hepatocyte growth factor. Finally, in a rat model of chronic heart failure induced by coronary ligation (n=14 to 15 rats per group), we found that intramyocardial slow release of fibroblast growth factor-2 with hepatocyte growth factor potently stimulates angiogenesis and arteriogenesis and prevents cardiac hypertrophy and fibrosis, as determined by immunohistochemistry, leading to improved cardiac perfusion after 3 months, as shown by magnetic resonance imaging. These multiple beneficial effects resulted in reduced adverse cardiac remodeling and improved left ventricular function, as revealed by echocardiography. Conclusion— Our data showing the selective advantage of using fibroblast growth factor-2 together with hepatocyte growth factor suggest that this growth factor combination may constitute an efficient novel treatment for chronic heart failure.
- Subjects :
- Male
[SDV.BIO]Life Sciences [q-bio]/Biotechnology
Angiogenesis
[SDV.MHEP.PHY] Life Sciences [q-bio]/Human health and pathology/Tissues and Organs [q-bio.TO]
medicine.medical_treatment
030204 cardiovascular system & hematology
Fibroblast growth factor
Neovascularization
Mice
0302 clinical medicine
Cell Movement
0303 health sciences
Mice, Inbred BALB C
Hepatocyte Growth Factor
[SDV.SP]Life Sciences [q-bio]/Pharmaceutical sciences
Coronary Vessels
3. Good health
[SDV.MHEP.CSC] Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular system
[SDV.SP] Life Sciences [q-bio]/Pharmaceutical sciences
Oncogene Protein v-akt
[SDV.IMM]Life Sciences [q-bio]/Immunology
Hepatocyte growth factor
Drug Therapy, Combination
Fibroblast Growth Factor 2
medicine.symptom
Signal transduction
Mitogen-Activated Protein Kinases
Cardiology and Cardiovascular Medicine
medicine.drug
[SDV.IMM] Life Sciences [q-bio]/Immunology
Neovascularization, Physiologic
Capsules
Cardiomegaly
03 medical and health sciences
[SDV.MHEP.CSC]Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular system
Physiology (medical)
medicine
[SDV.MHEP.PHY]Life Sciences [q-bio]/Human health and pathology/Tissues and Organs [q-bio.TO]
Animals
Rats, Wistar
Protein kinase B
030304 developmental biology
Cell Proliferation
Heart Failure
business.industry
Growth factor
Myocardium
medicine.disease
[SDV.BIO] Life Sciences [q-bio]/Biotechnology
Rats
Heart failure
Immunology
Chronic Disease
Cancer research
Angiogenesis Inducing Agents
business
Subjects
Details
- Language :
- English
- ISSN :
- 00097322 and 15244539
- Database :
- OpenAIRE
- Journal :
- Circulation, Circulation, American Heart Association, 2011, 124 (9), pp.1059-1069. ⟨10.1161/CIRCULATIONAHA.110.010264⟩, Circulation, 2011, 124 (9), pp.1059-1069. ⟨10.1161/CIRCULATIONAHA.110.010264⟩
- Accession number :
- edsair.doi.dedup.....54fc132e99f9b5464cd22c70fba5c465