Paracrine Engineering of Human Cardiac Stem Cells With Insulin-Like Growth Factor 1 Enhances Myocardial Repair
| Autor: | Terrence D. Ruddy, Duncan J. Stewart, N. Latham, Darryl R. Davis, Erik J. Suuronen, Bin Ye, Jared Strydhorst, Munir Boodhwani, Ghazaleh Rafatian, Robyn Jackson, Seth Mount, Vincent Chan, Everad L. Tilokee, Marc Ruel |
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| Rok vydání: | 2015 |
| Předmět: |
Time Factors
insulin-like growth factor 1 Cell Survival Cellular differentiation medicine.medical_treatment Receptor expression Paracrine Communication Myocardial Infarction heart failure Apoptosis Mice SCID Transfection Receptor IGF Type 1 Cell therapy Paracrine signalling Mice Inbred NOD Medicine Animals Humans Regeneration Myocytes Cardiac Insulin-Like Growth Factor I Cells Cultured Aged Cell Proliferation Original Research business.industry Growth factor Myocardium Stem Cells Cell Differentiation Genetic Therapy Middle Aged Coculture Techniques Rats Up-Regulation Mice Inbred C57BL Disease Models Animal Cytokine Immunology Cancer research cardiovascular system Stem cell cell therapy Cardiology and Cardiovascular Medicine business Stem Cell Transplantation |
| Zdroj: | Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease |
| ISSN: | 2047-9980 |
| Popis: | Background Insulin‐like growth factor 1 ( IGF ‐1) activates prosurvival pathways and improves postischemic cardiac function, but this key cytokine is not robustly expressed by cultured human cardiac stem cells. We explored the influence of an enhanced IGF ‐1 paracrine signature on explant‐derived cardiac stem cell–mediated cardiac repair. Methods and Results Receptor profiling demonstrated that IGF ‐1 receptor expression was increased in the infarct border zones of experimentally infarcted mice by 1 week after myocardial infarction. Human explant‐derived cells underwent somatic gene transfer to overexpress human IGF ‐1 or the green fluorescent protein reporter alone. After culture in hypoxic reduced‐serum media, overexpression of IGF ‐1 enhanced proliferation and expression of prosurvival transcripts and prosurvival proteins and decreased expression of apoptotic markers in both explant‐derived cells and cocultured neonatal rat ventricular cardiomyocytes. Transplant of explant‐derived cells genetically engineered to overexpress IGF ‐1 into immunodeficient mice 1 week after infarction boosted IGF ‐1 content within infarcted tissue and long‐term engraftment of transplanted cells while reducing apoptosis and long‐term myocardial scarring. Conclusions Paracrine engineering of explant‐derived cells to overexpress IGF ‐1 provided a targeted means of improving cardiac stem cell–mediated repair by enhancing the long‐term survival of transplanted cells and surrounding myocardium. |
| Databáze: | OpenAIRE |
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