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PMID: 11980881 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Intraocular adenoviral vector-mediated gene transfer in proliferative retinopathies.

Investigative ophthalmology & visual science ·Vol. 43 ·No. 5 ·2002-05-00 ·Pages 1610-5

Mori K, Gehlbach P, Ando A, Wahlin K, Gunther V, McVey D, Wei L, Campochiaro PA

Abstract

The purpose of this study was to compare levels and patterns of expression of reporter genes achieved with an E1-deleted and partially E3-deleted type 5 adenoviral (Ad) vector after intravitreous or subretinal injections, or after intravitreous injections in mouse eyes with proliferative retinopathies. Ad vectors containing reporter gene constructs were injected into the vitreous cavity or subretinal space of wild-type mice or mice with proliferative retinopathies, and quantitative comparisons were made of expression of transgenes. In normal eyes, peak Ad-mediated expression of luciferase, driven by a cytomegalovirus (CMV) promoter, occurred after injection of 10(7) to 10(8) viral particles and was 10 times greater after subretinal injections than after intravitreous injections. Intravitreous injections of Ad containing beta-galactosidase (LacZ) expression constructs (AdLacZ.10) resulted in strong expression of LacZ in epithelial cells of the iris and ciliary body and focal expression in the retina. Subretinal injections of AdLacZ.10 resulted in strong expression in RPE cells. Expression of LacZ after intravitreous injection of AdLacZ.10 was significantly greater in mice with two types of proliferative retinopathy (ischemic retinopathy or transgenic mice with retina-specific expression of platelet-derived growth factor (PDGF)-BB or PDGF-AB) than littermate control animals. Cells within epiretinal membranes and activated Müller cells were preferentially transduced in eyes with proliferative retinopathy. These data suggest that although higher intraocular expression levels can be achieved after subretinal injection of adenoviral vectors, intravitreous injections provide good transduction of cells lining the vitreous cavity. Compared with normal eyes, eyes with proliferative retinopathy showed increased transduction, which occurred preferentially in cells participating in the disease process. Intravitreous injection of adenoviral vectors containing appropriate expression constructs may provide a good strategy for acute treatment of proliferative retinopathies, such as diabetic retinopathy and proliferative vitreoretinopathy.

MeSH Terms
Adenoviridae/genetics Animals Gene Expression Gene Transfer Techniques Genes, Reporter/genetics Genetic Vectors Injections Lac Operon/genetics Mice Mice, Inbred C57BL Mice, Transgenic Models, Animal Pigment Epithelium of Eye/metabolism,pathology Platelet-Derived Growth Factor/genetics Retina/metabolism,pathology Retinal Diseases/genetics,metabolism,pathology Vitreous Body
Chemicals
Platelet-Derived Growth Factor
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Mori Keisuke
Departments of Ophthalmology and Neuroscience, The Johns Hopkins University School of Medicine, Maumenee 719, 600 N. Wolfe Street, Baltimore, MD 21287-9277, USA.
Gehlbach Peter
Ando Akira
Wahlin Karl
Gunther Vicky
McVey Duncan
Wei Lisa
Campochiaro Peter A
Article Info
Journal
Investigative ophthalmology & visual science
Abbr.
Invest Ophthalmol Vis Sci
ISSN
0146-0404
Published
2002-05-00
Pages
1610-5
Language
English
Region
United States
NLM ID
7703701
Subset
IM
Grants
NEI NIH HHS · EY 05951 · United States
NEI NIH HHS · EY 12609 · United States
NEI NIH HHS · K08 EY 13420 · United States
NEI NIH HHS · P30 EY 1765 · United States
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