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An Acute Injury Model for the Phenotypic Characteristics of Geographic Atrophy.
Bhutto, Imran A; Ogura, Shuntaro; Baldeosingh, Rajkumar; McLeod, D Scott; Lutty, Gerard A; Edwards, Malia M.
Affiliation
  • Bhutto IA; Department of Ophthalmology, Wilmer Eye Institute, Johns Hopkins Hospital, Baltimore, Maryland, United States.
  • Ogura S; Department of Ophthalmology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States.
  • Baldeosingh R; Department of Ophthalmology, Wilmer Eye Institute, Johns Hopkins Hospital, Baltimore, Maryland, United States.
  • McLeod DS; Department of Ophthalmology, Wilmer Eye Institute, Johns Hopkins Hospital, Baltimore, Maryland, United States.
  • Lutty GA; Department of Ophthalmology, Wilmer Eye Institute, Johns Hopkins Hospital, Baltimore, Maryland, United States.
  • Edwards MM; Department of Ophthalmology, Wilmer Eye Institute, Johns Hopkins Hospital, Baltimore, Maryland, United States.
Invest Ophthalmol Vis Sci ; 59(4): AMD143-AMD151, 2018 03 20.
Article in En | MEDLINE | ID: mdl-30208410
ABSTRACT

Purpose:

Geographic atrophy (GA) is the late stage of non-neovascular age-related macular degeneration. A lack of animal models for GA has hampered treatment efforts. Presented herein is a rat model for GA using subretinal injection of sodium iodate (NaIO3).

Methods:

Rats were given subretinal injections of NaIO3 (5 µg/µL) using a pico-injector. Fundus photographs and spectral domain optical coherent tomography scans were collected at 1, 3, 7, 14, and 28 days after injection, at which time rats were euthanized and eyes were enucleated. Eyes were either cryopreserved or dissected into retinal and choroidal flatmounts. Fluorescence immunohistochemistry was performed for retinal glial fibrillary acidic protein (activated Müller cells and astrocytes) and vimentin (Müller cells), as well as peanut agglutin lectin (photoreceptors) labeling. RPE/choroids were labeled for RPE65 and CD34. Images were collected on Zeiss confocal microscopes.

Results:

Fundus photos, spectral domain optical coherent tomography, and RPE65 staining revealed well-demarcated areas with focal loss of RPE and photoreceptors in NaIO3-treated rats. At 1 day after injection, RPE cells appeared normal. By 3 days, there was patchy RPE and photoreceptor loss in the injected area. RPE and photoreceptors were completely degenerated in the injected area by 7 days. A large subretinal glial membrane occupied the degenerated area. Choriocapillaris was highly attenuated in the injected area at 14 and 28 days.

Conclusions:

The rat model reported herein mimics the photoreceptor cell loss, RPE atrophy, glial membrane formation, and choriocapillaris degeneration seen in GA. This model will be valuable for developing and testing drugs and progenitor cell regenerative therapies for GA.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retina / Disease Models, Animal / Retinal Pigment Epithelium / Geographic Atrophy / Iodates Type of study: Prognostic_studies Limits: Animals Language: En Journal: Invest Ophthalmol Vis Sci Year: 2018 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retina / Disease Models, Animal / Retinal Pigment Epithelium / Geographic Atrophy / Iodates Type of study: Prognostic_studies Limits: Animals Language: En Journal: Invest Ophthalmol Vis Sci Year: 2018 Document type: Article Affiliation country:
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