RD3 gene delivery restores guanylate cyclase localization and rescues photoreceptors in the Rd3 mouse model of Leber congenital amaurosis 12

• Published in: Human molecular genetics Vol. 22; no. 19; pp. 3894 - 3905
• Main Authors: Molday, Laurie L, Djajadi, Hidayat, Yan, Paul, Szczygiel, Lukasz, Boye, Sanford L, Chiodo, Vince A, Gregory-Evans, Kevin, Sarunic, Marinko V, Hauswirth, William W, Molday, Robert S
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 01-10-2013
• Subjects: Animal models; Animals; Dependovirus - genetics; Disease Models, Animal; Endoplasmic Reticulum - genetics; Endoplasmic Reticulum - metabolism; Genetic Therapy; Genetic Vectors; Guanylate Cyclase - genetics; Guanylate Cyclase - metabolism; Guanylate Cyclase-Activating Proteins - genetics; Guanylate Cyclase-Activating Proteins - metabolism; Humans; Leber Congenital Amaurosis - genetics; Leber Congenital Amaurosis - metabolism; Leber Congenital Amaurosis - pathology; Leber Congenital Amaurosis - therapy; Mice; Mice, Inbred BALB C; Nuclear Proteins - genetics; Nuclear Proteins - metabolism; Nuclear Proteins - physiology; Retina - metabolism; Retinal Photoreceptor Cell Outer Segment - metabolism; Transgenes
• ISSN: 0964-6906; 1460-2083
• DOI: 10.1093/hmg/ddt244

RD3 is a 23 kDa protein implicated in the stable expression of guanylate cyclase in photoreceptor cells. Truncation mutations are responsible for photoreceptor degeneration and severe early-onset vision loss in Leber congenital amaurosis 12 (LCA12) patients, the rd3 mouse and the rcd2 collie. To further investigate the role of RD3 in photoreceptors and explore gene therapy as a potential treatment for LCA12, we delivered adeno-associated viral vector (AAV8) with a Y733F capsid mutation and containing the mouse Rd3 complementary DNA (cDNA) under the control of the human rhodopsin kinase promoter to photoreceptors of 14-day-old Rb(11.13)4Bnr/J and In (5)30Rk/J strains of rd3 mice by subretinal injections. Strong RD3 transgene expression led to the translocation of guanylate cyclase from the endoplasmic reticulum (ER) to rod and cone outer segments (OSs) as visualized by immunofluorescence microscopy. Guanylate cyclase expression and localization coincided with the survival of rod and cone photoreceptors for at least 7 months. Rod and cone visual function was restored in the In (5)30Rk/J strain of rd3 mice as measured by electroretinography (ERG), but only rod function was recovered in the Rb(11.13)4Bnr/J strain, suggesting that the latter may have another defect in cone phototransduction. These studies indicate that RD3 plays an essential role in the exit of guanylate cyclase from the ER and its trafficking to photoreceptor OSs and provide a 'proof of concept' for AAV-mediated gene therapy as a potential therapeutic treatment for LCA12.