Literature DB >> 25414197

Genetic background and light-dependent progression of photoreceptor cell degeneration in Prominin-1 knockout mice.

Margaret Dellett1, Noriaki Sasai1, Kenji Nishide2, Silke Becker1, Vasiliki Papadaki1, G Astrid Limb1, Anthony T Moore1, Toru Kondo3, Shin-Ichi Ohnuma1.   

Abstract

PURPOSE: Mutations in the Prominin-1 (Prom1) gene are known to cause retinitis pigmentosa and Stargardt disease, both of which are associated with progressive photoreceptor cell death. There are no effective therapies for either disorder. The aim of this study was to investigate the mechanism of the retinal degeneration in Prom1-deficient mouse models.
METHODS: We constructed Prom1 knockout mice with two distinct genetic backgrounds of C57BL/6 and C57BL/6xCBA/NSlc, and investigated the photoreceptor degeneration by means of histology and functional tests.. In addition, we examined the effect of light on the Prom1(-/-) retina by rearing the mice in the normal light/dark cycle and completely dark conditions. Finally, we investigated if the retinoic-acid derivative Fenretinide slowed the pace of retinal degeneration in these mouse models.
RESULTS: The Prom1(-/-)-knockout mice with both backgrounds developed photoreceptor degeneration after eye opening, but the CB57/BL6-background mice developed photoreceptor cell degeneration much faster than the C57BL/6xCBA/NSlc mice, demonstrating genetic background dependency.. Interestingly, our histologic and functional examination showed that the photoreceptor cell degeneration of Prom1-knockout mice was light-dependent, and was almost completely inhibited when the mutant mice were kept in the dark. The Prom1-knockout retina showed strong downregulation of expression of the visual cycle components, Rdh12 and Abca4. Furthermore, administration of Fenretinide, which lowers the level of the toxic lipofuscin, slowed the degeneration of photoreceptor cells.
CONCLUSIONS: These findings improve our understanding of the mechanism of cell death in Prominin-1-related disease and provide evidence that fenretinide may be worth studying in human disease. Copyright 2015 The Association for Research in Vision and Ophthalmology, Inc.

Entities:  

Keywords:  Prominin-1; Stargardt disease; fenretinide; light; modifier gene; photoreceptor degeneration; retinitis pigmentosa

Mesh:

Substances:

Year:  2014        PMID: 25414197     DOI: 10.1167/iovs.14-15479

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  11 in total

Review 1.  Photoreceptor Cilia and Retinal Ciliopathies.

Authors:  Kinga M Bujakowska; Qin Liu; Eric A Pierce
Journal:  Cold Spring Harb Perspect Biol       Date:  2017-10-03       Impact factor: 10.005

Review 2.  Genetic modifiers as relevant biological variables of eye disorders.

Authors:  Kacie J Meyer; Michael G Anderson
Journal:  Hum Mol Genet       Date:  2017-08-01       Impact factor: 6.150

3.  Whole exome sequencing analysis identifies novel Stargardt disease-related gene mutations in Chinese Stargardt disease and retinitis pigmentosa patients.

Authors:  Tsz Kin Ng; Yingjie Cao; Xiang-Ling Yuan; Shaowan Chen; Yanxuan Xu; Shao-Lang Chen; Yuqian Zheng; Haoyu Chen
Journal:  Eye (Lond)       Date:  2021-04-12       Impact factor: 3.775

4.  Commentary: "prom1 function in development, intestinal inflammation, and intestinal tumorigenesis".

Authors:  Christine A Fargeas; Edgar Büttner; Denis Corbeil
Journal:  Front Oncol       Date:  2015-04-21       Impact factor: 6.244

5.  Characteristic Ocular Features in Cases of Autosomal Recessive PROM1 Cone-Rod Dystrophy.

Authors:  Frederick T Collison; Gerald A Fishman; Takayuki Nagasaki; Jana Zernant; J Jason McAnany; Jason C Park; Rando Allikmets
Journal:  Invest Ophthalmol Vis Sci       Date:  2019-05-01       Impact factor: 4.799

Review 6.  Therapy Approaches for Stargardt Disease.

Authors:  Elena Piotter; Michelle E McClements; Robert E MacLaren
Journal:  Biomolecules       Date:  2021-08-09

7.  Early manifestations and differential gene expression associated with photoreceptor degeneration in Prom1-deficient retina.

Authors:  Yuka Kobayashi; Shizuka Watanabe; Agnes Lee Chen Ong; Manabu Shirai; Chiemi Yamashiro; Tadahiko Ogata; Fumiaki Higashijima; Takuya Yoshimoto; Takahide Hayano; Yoshiyuki Asai; Noriaki Sasai; Kazuhiro Kimura
Journal:  Dis Model Mech       Date:  2021-11-24       Impact factor: 5.758

8.  Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease.

Authors:  Jana Zernant; Winston Lee; Jun Wang; Kerry Goetz; Ehsan Ullah; Takayuki Nagasaki; Pei-Yin Su; Gerald A Fishman; Stephen H Tsang; Santa J Tumminia; Brian P Brooks; Robert B Hufnagel; Rui Chen; Rando Allikmets
Journal:  PLoS Genet       Date:  2022-03-30       Impact factor: 5.917

9.  Prominin 1 and Notch regulate ciliary length and dynamics in multiciliated cells of the airway epithelium.

Authors:  Carlos F H Serra; Helu Liu; Jun Qian; Munemasa Mori; Jining Lu; Wellington V Cardoso
Journal:  iScience       Date:  2022-07-14

Review 10.  Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss.

Authors:  Gayle B Collin; Navdeep Gogna; Bo Chang; Nattaya Damkham; Jai Pinkney; Lillian F Hyde; Lisa Stone; Jürgen K Naggert; Patsy M Nishina; Mark P Krebs
Journal:  Cells       Date:  2020-04-10       Impact factor: 7.666

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