Abstract
Purpose. To evaluate ocular sites of expression of the tissue inhibitor of metalloproteinase-3 gene (TIMP-3). Methods. In situ hybridization was performed on frozen sections of albino mouse eyes using riboprobes generated to the 3' untranslated region of TIMP-3. Results. TIMP-3 mRNA expression was detected strongly in the retinal pigment epithelium (RPE) and to a minor extent in the ciliary epithelium, but not at any other site within the eye. Conclusions. Expression of TIMP-3 in the RPE is consistent with the recent demonstration of TIMP-3 mutations in patients with Sorsby's fundus dystrophy, a condition marked by the early onset of choroidal neovascularization in the macula. Unlike many of the recently described genes that cause human retinal disease, TIMP-3 is preferentially expressed in the RPE of the normal eye, as opposed to the photoreceptors.
Original language | English (US) |
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Pages (from-to) | 1921-1924 |
Number of pages | 4 |
Journal | Investigative Ophthalmology and Visual Science |
Volume | 37 |
Issue number | 9 |
State | Published - Aug 1996 |
Keywords
- extracellular matrix
- neovascularization
- proteinases
- retinal pigment epithelium
- tissue inhibitor of metalloproteinases-3
ASJC Scopus subject areas
- Ophthalmology
- Sensory Systems
- Cellular and Molecular Neuroscience