Adeno-associated virus-mediated gene transfer into human retinal pigment epithelium cells

Australian and New Zealand Journal of Ophthalmology

Volumn 26, Issue SUPPL. 1, 1998, Pages

  Lai, Y K Y ^a,b   Rakoczy, P ^a   Constable, I ^a   Rolling, F ^b  

^a UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^b LIONS EYE INSTITUTE   (Australia)

Author keywords

Adeno associated virus; Gene therapy; Green fluorescent protein; Retinal pigment epithelium

Indexed keywords

GREEN FLUORESCENT PROTEIN; NEOMYCIN;

ADENO ASSOCIATED VIRUS; ARTICLE; GENE; GENE THERAPY; GENE TRANSFER; HUMAN; HUMAN CELL; PIGMENT EPITHELIUM;

EID: 0031862194     PISSN: 08149763     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1442-9071.1998.tb01381.x     Document Type: Article

References (10)

1. Davis A, Bernstein P, Bok D, Turner J, Nachtigal M, Hunt R. A human retinal pigment epithelial cell line that retains epithelial characteristics after prolonged culture. Invest. Ophthalmol. Vis. Sci. 1995; 36: 955-64.
2. Ali R, Reichel M, Thrasher A et al. Gene transfer into the mouse retina mediated by an adeno-associated viral vector. Hum. Mol. Genet. 1996; 5: 591-4.
3. Berns K, Giraud C. Biology of adeno-associated virus. In: Berns K, Giraud C (eds). Adeno-associated virus (AAV) vectors in gene therapy. Berlin: Springer-Verlag, 1996; 1-24.
4. Xiao X, Xiao W, Li J, Samulski R. A novel 165-base-pair terminal repeat sequence is the sole cis requirement for the adeno-associated virus life cycle. J. Virol. 1997; 71: 941-8.
5. Samulski R, Zhu X, Xiao X et al. Targeted integration of adeno-associated virus (AAV) into human chromosome 19. EMBO J. 1991; 10: 3941-50.
6. Xiao X, Samulski R. Efficient long-term gene transfer into muscle tissue of immunocompetent mice by adeno-associated virus vector. J. Virol. 1996; 70: 8098-108.
7. Graham F, Smiley J, Russell W, Nairu R. Characteristics of a human cell line transformed by DNA from human adenovirus type 5. J. Gen. Virol 1977; 36: 59-72.
8. Samulski R, Chang L, Shenk T. Helper-free stocks of recombinant adeno-associated viruses: Normal integration does not require viral gene expression. J. Virol. 1989; 63: 3822-8.
9. Rolling F, Samulski R. AAV as a viral vector for human gene therapy. Generation of recombinant virus. Mol. Biotechn. 1995; 3: 9-15.
10. Kotin R, Berns K. Organization of adeno-associated virus DNA in latently infected Detroit 6 cells. Virology 1989; 170: 460-7.