Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024 Oct 1;14(10):a041311.
doi: 10.1101/cshperspect.a041311.

Rodent Models of Retinal Degeneration: From Purified Cells in Culture to Living Animals

Affiliations
Review

Rodent Models of Retinal Degeneration: From Purified Cells in Culture to Living Animals

Valérie Fradot et al. Cold Spring Harb Perspect Med. .

Abstract

Rodent models of retinal degeneration are essential for the development of therapeutic strategies. In addition to living animal models, we here also discuss models based on rodent cell cultures, such as purified retinal ganglion cells and retinal explants. These ex vivo models extend the possibilities for investigating pathological mechanisms and assessing the neuroprotective effect of pharmacological agents by eliminating questions on drug pharmacokinetics and bioavailability. The number of living rodent models has greatly increased with the possibilities to achieve transgenic modifications in animals for knocking in and out genes and mutations. The Cre-lox system has further enabled investigators to target specific genes or mutations in specific cells at specific stages. However, chemically or physically induced models can provide alternatives to such targeted gene modifications. The increased diversity of rodent models has widened our possibility to address most ocular pathologies for providing initial proof of concept of innovative therapeutic strategies.

PubMed Disclaimer

References

    1. Abdeljalil J, Hamid M, Abdel-mouttalib O, Stéphane R, Raymond R, Johan A, José S, Pierre C, Serge P. 2005. The optomotor response: a robust first-line visual screening method for mice. Vision Res 45: 1439–1446. 10.1016/j.visres.2004.12.015 - DOI - PubMed
    1. Aït-Ali N, Fridlich R, Millet-Puel G, Clérin E, Delalande F, Jaillard C, Blond F, Perrocheau L, Reichman S, Byrne LC, et al. 2015. Rod-derived cone viability factor promotes cone survival by stimulating aerobic glycolysis. Cell 161: 817–832. 10.1016/j.cell.2015.03.023 - DOI - PubMed
    1. Ali RR, Sarra GM, Stephens C, Alwis MD, Bainbridge JW, Munro PM, Fauser S, Reichel MB, Kinnon C, Hunt DM, et al. 2000. Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy. Nat Genet 25: 306–310. 10.1038/77068 - DOI - PubMed
    1. Arnault E, Barrau C, Nanteau C, Gondouin P, Bigot K, Viénot F, Gutman E, Fontaine V, Villette T, Cohen-Tannoudji D, et al. 2013. Phototoxic action spectrum on a retinal pigment epithelium model of age-related macular degeneration exposed to sunlight normalized conditions. PLoS ONE 8: e71398. 10.1371/journal.pone.0071398 - DOI - PMC - PubMed
    1. Balse E, Tessier LH, Fuchs C, Forster V, Sahel JA, Picaud S. 2005. Purification of mammalian cone photoreceptors by lectin panning and the enhancement of their survival in glia-conditioned medium. Invest Ophthalmol Vis Sci 46: 367–374. 10.1167/iovs.04-0695 - DOI - PubMed

LinkOut - more resources