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- Title
AAV-mediated Tyrosinase Gene Transfer Restores Melanogenesis and Retinal Function in a Model of Oculo-cutaneous Albinism Type I (OCA1).
- Authors
Gargiulo, Annagiusi; Bonetti, Ciro; Montefusco, Sandro; Neglia, Simona; Di Vicino, Umberto; Marrocco, Elena; Corte, Michele Della; Domenici, Luciano; Auricchio, Alberto; Surace, Enrico M.
- Abstract
Oculo-cutaneous albinism type 1 (OCA1) is characterized by congenital hypopigmentation and is due to mutations in the TYROSINASE gene (TYR). In this study, we have characterized the morpho-functional consequences of the lack of tyrosinase activity in the spontaneous null mouse model of OCA1 (Tyrc-2j). Here, we show that adult Tyrc-2j mice have several retinal functional anomalies associated with photoreceptor loss. To test whether these anomalies are reversible upon TYR complementation, we performed intraocular administration of an adeno-associated virus (AAV)–based vector, encoding the human TYR gene, in adult Tyrc-2j mice. This resulted in melanosome biogenesis and ex novo synthesis of melanin in both neuroectodermally derived retinal pigment epithelium (RPE) and in neural crest–derived choroid and iris melanocytes. Ocular melanin accumulation prevented progressive photoreceptor degeneration and resulted in restoration of retinal function. Our results reveal novel properties of pigment cells and show that the developmental anomalies of albino mice are associated with defects occurring in postnatal life, adding novel insights on OCA1 disease pathogenesis. In addition, we provide proof-of-principle of an effective gene-based strategy relevant for future application in albino patients.Molecular Therapy (2009) 17 8, 1347–1354. doi:10.1038/mt.2009.112
- Subjects
GENETIC transformation; MELANOGENESIS; GENE expression; PHENOL oxidase; ALBINOS &; albinism; EPITHELIAL cells
- Publication
Molecular Therapy, 2009, Vol 17, Issue 8, p1347
- ISSN
1525-0016
- Publication type
Article
- DOI
10.1038/mt.2009.112