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Ex vivo gene transfer of basic fibroblast growth factor improves cardiac function and blood flow in a swine chronic myocardial ischemia model

Abstract

We previously reported adenovirus-mediated ex vivo gene transfer of basic fibroblast growth factor (bFGF) as a new treatment for leg ischemia. This time, we tested this method on a swine myocardial ischemia model, seeking the possibility of its application for ischemic heart disease. An ameroid constrictor was placed around the proximal left circumflex branch of pigs to induce myocardial ischemia. Simultaneously, a skin section was harvested and fibroblasts were cultured. Fibroblasts were then infected with adenovirus vector containing a bFGF cDNA with a secretory signal sequence (bFGF group, n=8) or a LacZ cDNA (control group, n=8). At 28 days after constrictor implantation, 2.5 × 106 fibroblasts were administered into each of the right and left coronary arteries. The injected fibroblasts accumulated in the myocardium without causing myocardial ischemia. Echocardiography, electromechanical mapping and coronary arteriography were conducted just before and 28 days after fibroblast injection, and regional left ventricular myocardial blood flow was measured 28 days after fibroblast injection. These evaluations revealed that the bFGF group exhibited significant development of collateral vessels and improvement of myocardial contraction in the ischemic area compared with the control group. We believe that this method is a promising treatment strategy for ischemic heart disease.

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References

  1. Yanagisawa-Miwa A et al. Salvage of infarcted myocardium by angiogenic action of basic fibroblast growth factor. Science 1992; 257: 1401–1403.

    Article  CAS  Google Scholar 

  2. Banai S et al. Angiogenic-induced enhancement of collateral blood flow to ischemic myocardium by vascular endothelial growth factor in dogs. Circulation 1994; 89: 2183–2189.

    Article  CAS  Google Scholar 

  3. Losordo DW et al. Gene therapy for myocardial angiogenesis: initial clinical results with direct myocardial injection of phVEGF165 as sole therapy for myocardial ischemia. Circulation 1998; 25: 2800–2804.

    Article  Google Scholar 

  4. Vale PR et al. Randomized, single-blind, placebo-controlled pilot study of catheter-based myocardial gene transfer for therapeutic angiogenesis using left ventricular electromechanical mapping in patients with chronic myocardial ischemia. Circulation 2001; 103: 2138–2143.

    Article  CAS  Google Scholar 

  5. Ohara N et al. Adenovirus-mediated ex vivo gene transfer of basic fibroblast growth factor promotes collateral development in a rabbit model of hind limb ischemia. Gene Therapy 2001; 8: 837–845.

    Article  CAS  Google Scholar 

  6. Suzuki K et al. Development of a novel method for cell transplantation through the coronary artery. Circulation 2000; 102(Suppl III): 359–364.

    Google Scholar 

  7. Lee RJ et al. VEGF gene delivery to myocardium: deleterious effects of unregulated expression. Circulation 2000; 102: 898–901.

    Article  CAS  Google Scholar 

  8. Miyake S et al. Efficient generation of recombinant adenoviruses using adenovirus DNA-terminal protein complex and a cosmid bearing the full-length virus genome. Proc Natl Acad Sci USA 1996; 93: 1320–1324.

    Article  CAS  Google Scholar 

  9. Akimoto M et al. Adenovirally expressed basic fibroblast growth factor rescues photoreceptor cells in RCS rats. Invest Ophthalmol Vis Sci 1999; 40: 273–279.

    CAS  Google Scholar 

  10. Sasada R et al. Expression of modified bFGF cDNAs in mammalian cells. Ann NY Acad Sci 1991; 638: 149–160.

    Article  CAS  Google Scholar 

  11. Koyama H, Reidy MA . Reinjury of arterial lesions induces intimal smooth muscle cell replication that is not controlled by fibroblast growth factor 2. Circ Res 1997; 80: 408–417.

    Article  CAS  Google Scholar 

  12. Ben-Haim SA et al. Nonfluoroscopic, in vivo navigation and mapping technology. Nat Med 1996; 2: 1393–1395.

    Article  CAS  Google Scholar 

  13. Gepstein L, Hayam G, Ben-Haim SA . A novel method for nonfluoroscopic catheter-based electroanatomical mapping of the heart: in vitro and in vivo accuracy results. Circulation 1997; 95: 1611–1622.

    Article  CAS  Google Scholar 

  14. Rentrop KP et al. Changes in collateral channel filling immediately after controlled coronary artery occlusion by an angioplasty balloon in human subjects. J Am Coll Cardiol 1985; 5: 587–592.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This study was supported by a Grant-in Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan. We thank Yasuo Ohashi, PhD (Professor of Biostatistics, School of Health Sciences and Nursing, University of Tokyo) for statistical advice.

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Ninomiya, M., Koyama, H., Miyata, T. et al. Ex vivo gene transfer of basic fibroblast growth factor improves cardiac function and blood flow in a swine chronic myocardial ischemia model. Gene Ther 10, 1152–1160 (2003). https://doi.org/10.1038/sj.gt.3301984

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