Adeno-associated virus-mediated gene transfer into rat carotid arteries

Gene Therapy

Volumn 4, Issue 8, 1997, Pages 757-761

  Rolling, F ^a   Nong, Z ^a   Pisvin, S ^a   Collen, D ^a,b  

^a DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^b UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Adeno associated virus; Carotid; Vessel wall; galactosidase

Indexed keywords

ADENO ASSOCIATED VIRUS; ADVENTITIA; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTERY INJURY; ARTERY MEDIA; ARTERY WALL; ARTICLE; CAROTID ARTERY; GENE THERAPY; GENE TRANSFER; NONHUMAN; PRIORITY JOURNAL; RAT; REPORTER GENE; VASCULAR DISEASE;

ADENO-ASSOCIATED VIRUS; ANIMALIA;

EID: 0030866312     PISSN: 09697128     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.gt.3300465     Document Type: Article

References (36)

1. Flugelman MY et al. Low level in vivo gene transfer into the arterial wall through a perforated balloon catheter. Circulation 1992; 85: 1110-1117.
2. Guzman RJ et al. Efficient and selective adenovirus-mediated gene transfer into vascular neointima. Circulation 1993; 88: 2838-2848.
3. Leclerc G et al. Percutaneous arterial gene transfer in a rabbit model. J Clin Invest 1992; 90: 936-944.
4. Lee SW et al. In vivo adenoviral vector-mediated gene transfer into balloon-injured rat carotid arteries. Circ Res 1993; 73: 797-807.
5. Lemarchand P, Jones M, Yamada I, Crystal RG. In vivo gene transfer and expression in normal uninjured blood vessels using replication-deficient recombinant adenovirus vectors. Circ Res 1993; 72: 1132-1138.
6. Lim CS et al. Direct in vivo gene transfer into the coronary and peripheral vasculatures of the intact dog. Circulation 1990; 83: 2007-2011.
7. Lynch CM et al. Long-term expression of human adenosine deaminase in vascular smooth muscle cells of rats: a model for gene therapy. Proc Natl Acad Sci USA 1992; 89: 1138-1142.
8. Nabel EG et al. Recombinant gene expression in vivo within endothelial cells of the arterial wall. Science 1989; 244: 1342-1344.
9. Nabel EG, Plautz G, Nabel GJ. Site-specific gene expression in vivo by direct gene transfer into the arterial wall. Science 1990; 249: 1285-1288.
10. Rios CD et al. Adenovirus-mediated gene transfer to normal and atherosclerotic arteries. A novel approach. Arterioscler Thromb Vase Biol 1995; 15: 2241-2245.
11. Rome JJ et al. Anatomic barriers influence the distribution of in vivo gene transfer into the arterial wall. Modeling with microscopic tracer particles and verification with a recombinant adenoviral vector. Arterioscler Thromb 1994; 14: 148-161.
12. Nabel EG, Nabel GJ. Complex models for the study of gene function in cardiovascular biology. Annu Rev Physiol 1994; 56: 741-761.
13. Lee SW et al. In vivo adenoviral-mediated gene transfer into balloon-injured rat carotid arteries. Circ Res 1993; 73: 797-807.
14. Samulski RJ, Chang L-S, Shenk T. Helper-free stocks of recombinant adeno-associated viruses: normal integration does not require viral gene expression. J Virol 1989; 63: 3822-3828.
15. Afione SA et al. In vivo model of adeno-associated virus vector persistence and rescue. J Virol 1996; 70: 3235-3241.
16. Flotte TR et al. Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vector. Proc Natl Acad Sci USA 1993; 90: 10613-10617.
17. Zhou SZ et al. Adeno-associated virus 2-mediated gene transfer in murine hematopoietic progenitor cells. Exp Hematol 1993; 21: 928-933.
18. LaFace D, Hermonat P, Wakeland E, Peck A. Gene transfer into hematopoietic progenitor cells mediated by an adeno-associated virus vector. Virology 1988; 162: 483-486.
19. Mendelson E et al. Replication of adeno-associated virus type 2 in human lymphocytic cells and interaction with HIV-1. Virology 1992; 187: 453-463.
20. Walsh CE et al. Regulated high level expression of a human gamma-globin gene introduced into erythroid cells by an adenoassociated virus vector. Proc Natl Acad Sci USA 1992; 89: 7257-7261.
21. Einerhand MPW et al. Regulated high-level human β-globin gene expression in erythroid cells following recombinant adenoassociated virus-mediated gene transfer. Gene Therapy 1995; 2: 336-343.
22. Flotte TR et al. Expression of the cystic fibrosis transmembrane conductance regulator from a novel adeno-associated virus promoter. J Biol Chem 1993; 268: 3781-3790.
23. Podsakoff G, Wong KK Jr, Chatterjee S. Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors. J Virol 1994; 68: 5656-5666.
24. Russell DW, Miller AD, Alexander IE. Adeno-associated virus vectors preferentially transduce cells in S phase. Proc Natl Acad Sci USA 1994; 91: 8915-8919.
25. Alexander IA, Russell DW, Spence AM, Miller AD. Effects of gamma irradiation on the transduction of dividing and nondividing cells in brain and muscle of rats by adeno-associated virus vectors. Hum Gene Ther 1996; 7: 841-850.
26. McCown TJ et al. Differential and persistent expression patterns of CNS gene transfer by an adeno-associated virus (AAV) vector. Brain Res 1996; 713: 99-107.
27. Xiao X, Li J, Samulski RJ. Efficient long-term gene transfer into muscle tissue of immunocompetent mice by adeno-associated virus vector. J Virol 1996; 70: 8098-8108.
28. Clowes AW, Reidy MA, Clowes MM. Kinetics of cellular proliferation after arterial injury. I. smooth muscle growth in the absence of endothelium. Lab Invest 1983; 49: 327-333.
29. Russell DW, Miller AD, Alexander IE. Adeno-associated virus vectors preferentially transduce cells in S phase. Proc Natl Acad Sci USA 1994; 91: 8915-8919.
30. Andersen HR, Maeng M, Thorwest M, Falk E. Remodeling rather than neointimal formation explains luminal narrowing after deep vessel wall injury. Circulation 1996; 93: 1716-1724.
31. Shi Y et al. Adventitial remodeling after coronary arterial injury. Circulation 1996; 93: 340-348.
32. Shi Y et al. Adventitial myofibroblast contribute to neointimal formation in injured porcine coronary arteries. Circulation 1996; 94: 1655-1664.
33. Goodman S et al. Recombinant adeno-associated virus-mediated gene transfer into hematopoietic progenitor cells. Blood 1994; 84: 1492-1500.
34. Rolling F, Samulski RJ. AAV as a viral vector for human gene therapy. Generation of recombinant virus. Mol Biotechnol 1995; 3: 9-15.
35. Graham FL, Prevec L. Manipulation of adenovirus vectors In: Murray EJ (ed). Methods in Molecular Biology: Gene Transfer and Expression Protocols. Humana Press: Clifton, NJ, 1991; 7: 109-128.
36. Edgell CJS, McDonald CC, Graham JB. Permanent cell line expressing factor VIII related antigen established by hybridization. Proc Natl Acad Sci USA 1983; 80: 3734-3737.