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Longitudinal evaluation of expression of virally delivered transgenes in gerbil cone photoreceptors

Published online by Cambridge University Press:  03 July 2008

MATTHEW C. MAUCK*
Affiliation:
Departments of Cell Biology, Neurobiology, and Anatomy, Medical College of Wisconsin, Milwaukee, Wisconsin
KATHERINE MANCUSO
Affiliation:
Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, Wisconsin
JAMES A. KUCHENBECKER
Affiliation:
Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, Wisconsin
THOMAS B. CONNOR
Affiliation:
Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, Wisconsin
WILLIAM W. HAUSWIRTH
Affiliation:
Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, Florida
JAY NEITZ
Affiliation:
Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, Wisconsin
MAUREEN NEITZ
Affiliation:
Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, Wisconsin
*
Address correspondence and reprint requests to: Matthew C. Mauck, Departments of Cell Biology, Neurobiology, and Anatomy, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226. E-mail: [email protected]

Abstract

Delivery of foreign opsin genes to cone photoreceptors using recombinant adeno-associated virus (rAAV) is a potential tool for studying the basic mechanisms underlying cone based vision and for treating vision disorders. We used an in vivo retinal imaging system to monitor, over time, expression of virally-delivered genes targeted to cone photoreceptors in the Mongolian gerbil (Meriones unguiculatus). Gerbils have a well-developed photopic visual system, with 11–14% of their photoreceptors being cones. We used replication deficient serotype 5 rAAV to deliver a gene for green fluorescent protein (GFP). In an effort to direct expression of the gene specifically to either S or M cones, the transgene was under the control of either the human X-chromosome opsin gene regulatory elements, i.e., an enhancer termed the locus control region (LCR) and L promoter, or the human S-opsin promoter. Longitudinal fluorescence images reveal that gene expression is first detectable about 14 days post-injection, reaches a peak after about 3 months, and is observed more than a year post-injection if the initial viral concentration is sufficiently high. The regulatory elements are able to direct expression to a subpopulation of cones while excluding expression in rods and non-photoreceptor retinal cells. When the same viral constructs are used to deliver a human long-wavelength opsin gene to gerbil cones, stimulation of the introduced human photopigment with long-wavelength light produces robust cone responses.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2008

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References

REFERENCES

Acland, G.M., Aguirre, G.D., Bennett, J., Aleman, T.S., Cideciyan, A.V., Bennicelli, J., Dejneka, N.S., Pearce-Kelling, S.E., Maguire, A.M., Palczewski, K., Hauswirth, W.W. & Jacobson, S.G. (2005). Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindness. Molecular Therapy 12, 10721082.CrossRefGoogle Scholar
Acland, G.M., Aguirre, G.D., Ray, J., Zhang, Q., Aleman, T.S., Cideciyan, A.V., Pearce-Kelling, S.E., Anand, V., Zeng, Y., Maguire, A.M., Jacobson, S.G., Hauswirth, W.W. & Bennett, J. (2001). Gene therapy restores vision in a canine model of childhood blindness. Nature Genetics 28, 9295.CrossRefGoogle Scholar
Alexander, J.J., Umino, Y., Everhart, D., Chang, B., Min, S.H., Li, Q., Timmers, A.M., Nawes, N.L., Pang, J., Barlow, R.B. & Hauswirth, W.W. (2007). Restoration of cone vision in a mouse model of achromatopsia. Nature Medicine 13, 685687.CrossRefGoogle Scholar
Applebury, M.L., Antoch, M.P., Baxter, L.C., Chun, L.L.Y., Kalk, J.D., Farhangfar, F., Kage, K., Krzystolik, M.G., Lyass, L.A. & Robbins, J.T. (2000). The murine cone photoreceptor: A single cone type expresses both S and M opsins with retinal spatial patterning. Neuron 27, 513523.CrossRefGoogle Scholar
Bainbridge, J.W.B., Tan, M.H. & Ali, R.R. (2006). Gene therapy progress and prospects: The eye. Gene Therapy 13, 11911197.CrossRefGoogle ScholarPubMed
Bainbridge, J.W., Mistry, A., Schlichtenbrede, F.C., Smith, A., Broderick, C., De Alwis, M., Georgiadis, A., Taylor, P.M., Squires, M., Sethi, C., Charteris, D., Thrasher, A.J., Sargan, D. & Ali, R.R. (2003). Stable rAAV-mediated transduction of rod and cone photoreceptors in the canine retina. Gene Therapy 10, 13361344.Google Scholar
Bennett, J., Duan, D., Engelhardt, J.F. & Maguire, A.M. (1997). Real-time, noninvasive in vivo assessment of adeno-associated virus-mediated retinal transduction. Investigative Ophthalmology and Vision Research 38, 25872863.Google ScholarPubMed
Bennett, J., Maguire, A.M., Cideciyan, V., Schnell, M., Glover, E., Anand, V., Aleman, T.S., Chirmule, N., Gupta, A.R., Huang, Y., Gao, G.-P., Nyberg, W.C., Tazelaar, J., Hughes, J., Wilson, J.M. & Jacobson, S.G. (1999). Stable transgene expression in rod photoreceptors after recombinant adeno-associated virus-mediated gene transfer to monkey retina. Proceedings of the National Academy of Sciences USA 96, 99209925.CrossRefGoogle ScholarPubMed
Carroll, J., Neitz, M. & Neitz, J. (2002). Estimates of L:M cone ratio from ERG flicker photometry and genetics. Journal of Vision 2, 531542.CrossRefGoogle ScholarPubMed
Daniels, D.M., Shen, W.Y., Constable, I.J. & Rakoczy, P.E. (2003). Quantitative model demonstrating that recombinant adeno-associated virus and green fluorescent protein are non-toxic to the rat retina. Clinical Experimental Ophthalmology 31, 439444.Google Scholar
Glushakova, L.G., Timmers, A.M., Pang, J., Teusner, J.T. & Hauswirth, W.W. (2006). Human blue-opsin promoter preferentially targets reporter gene expression to rat s-cone photoreceptors. Investigative Ophthalmology and Vision Research 47, 35053513.CrossRefGoogle ScholarPubMed
Govardovskii, V.I., Rohlich, P., Szel, A. & Khokhlova, T.V. (1992). Cones in the retina of the mongolian gerbil, Meriones unguiculatus: An immunocytochemical and electrophysiological study. Vision Research 32, 1927.CrossRefGoogle ScholarPubMed
Jacobs, G.H., Williams, G.A., Cahill, H. & Nathans, J. (2007). Emergence of novel color vision in mice engineered to express a human cone photopigment. Science 315, 17231725.Google Scholar
Kuchenbecker, J.A., Sahay, M., Tait, D.M., Neitz, M. & Neitz, J. (2008). Topography of the long- to middle-wavelength sensitive cone ratio in the human retina assessed with a wide-field color multifocal electroretinogram. Visual Neuroscience 25, 301306.CrossRefGoogle Scholar
LeMeur, G., Weber, M., Yann, P., Mendes-Madeira, A., Nivard, D., Deschamps, J., Moullier, P. & Rolling, F. (2005). Postsurgical assessment and long-term safety of recombinant adeno-associated virus-mediated gene transfer into the retinas of dogs and primates. Archives of Ophthalmology 123, 500506.CrossRefGoogle Scholar
Li, Q., Timmers, A.M., Guy, J., Pang, J. & Hauswirth, W.W. (2007). Cone-specific expression using a human red opsin promoter in recombinant AAV. Vision Research 48, 332338.CrossRefGoogle ScholarPubMed
Mancuso, K., Hendrickson, A.E., Connor, T.B. Jr., Mauck, M.C., Kinsella, J.J., Hauswirth, W.W., Neitz, J. & Neitz, M. (2007). Recombinant adeno-associated virus targets passenger gene expression to cones in primate retina. Journal of the Optical Society of America A Optics, Image Science, and Vision 24, 14111416.CrossRefGoogle ScholarPubMed
Nathans, J., Thomas, D. & Hogness, D.S. (1986). Molecular genetics of human color vision: The genes encoding blue, green, and red pigments. Science 232, 193202.CrossRefGoogle ScholarPubMed
Pang, J.J., Chang, B., Kumar, A., Nusinowitz, S., Noorwez, S.M., Li, J., Rani, A., Foster, T.C., Chiodo, V.A., Doyle, T., Li, H., Malhotra, R., Teusner, J.T., McDowell, J.H., Min, S.H., Li, Q., Kaushal, S. & Hauswirth, W.W. (2006). Gene therapy restores vision-dependent behavior as well as retinal structure and function in a mouse model of RPE65 Leber congenital amaurosis. Molecular Therapy 13, 565572.Google Scholar
Rohlich, P., van Veen, T. & Szel, A. (1994). Two different visual pigments in one retinal cone cell. Neuron 13, 11591166.Google Scholar
Rolling, F., Shen, W., Tabarias, H., Constable, I., Kanagasingam, Y., Barry, C.J. & Rakoczy, P.E. (1999). Evaluation of adeno-associated virus-mediated gene transfer into the rat retina by clincal fluorescence photography. Human Gene Therapy 10, 641648.CrossRefGoogle Scholar
Smallwood, P.M., Olveczky, B.P., Williams, G.L., Jacobs, G.H., Reese, B.E., Meister, M. & Nathans, J. (2003). Genetically engineered mice with an additional class of cone photoreceptors: Implications for the evolution of color vision. Proceedings of the National Academy of Sciences of the United States of America 100, 1170611711.CrossRefGoogle ScholarPubMed
Wang, Y., Macke, J.P., Merbs, S.L., Zack, D.J., Klaunberg, B., Bennett, J., Gearhart, J. & Nathans, J. (1992). A locus control region adjacent to the human red and green visual pigment genes. Neuron 9, 429440.CrossRefGoogle Scholar
Wikler, K.C., Perez, G. & Finlay, B.L. (1989). Duration of retinogenesis: its relationshop to retinal organization in two cricetine rodents. The Journal of Comparative Neurology 285, 157176.Google Scholar