Literature DB >> 22395892

Autosomal recessive retinitis pigmentosa due to ABCA4 mutations: clinical, pathologic, and molecular characterization.

Robert F Mullins1, Markus H Kuehn, Roxana A Radu, G Stephanie Enriquez, Jade S East, Emily I Schindler, Gabriel H Travis, Edwin M Stone.   

Abstract

PURPOSE: Autosomal recessive retinitis pigmentosa (ARRP) is a genetically heterogeneous condition characterized by progressive loss of retinal photoreceptor cells. In order to gain new insights into the pathogenesis of ARRP, we evaluated the morphological, biochemical, and gene expression changes in eyes from a human donor with ARRP due to mutations in the ABCA4 gene.
METHODS: Eyes were obtained postmortem from a donor with end-stage retinitis pigmentosa. The coding sequences of the RDS, RHO, and ABCA4 genes were screened for disease-causing mutations. Morphological changes in different regions of the retina were examined histologically, and levels of lipofuscin-associated bisretinoids were measured. Gene expression was examined in retinal/choroidal tissue using microarray analysis, and all parameters were compared to those in unaffected control donors.
RESULTS: Genetic analysis of the donor's DNA identified two mutations in the ABCA4 gene, IVS14+1G > C and Phe1440del1 cT, each on a separate allele. Morphological evaluation revealed complete loss of the outer nuclear layer, remodeling of the inner retina, loss of retinal vasculature, and regional neovascularization. The retinal pigment epithelium and choriocapillaris exhibited regional preservation. Microarray analysis revealed loss of photoreceptor cell-associated transcripts, with preservation of multiple genes expressed specifically in inner retinal neurons.
CONCLUSIONS: The persistence of transcripts expressed by inner retinal neurons suggests that despite significant plasticity that occurs during retinal degeneration, bipolar cells and ganglion cells remain at least partially differentiated. Findings from this study suggest that some forms of therapy currently under investigation may have benefit even in advanced retinal degeneration.

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Year:  2012        PMID: 22395892      PMCID: PMC3995570          DOI: 10.1167/iovs.12-9477

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


  46 in total

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2.  Glycoconjugates of choroidal neovascular membranes in age-related macular degeneration.

Authors:  Robert F Mullins; Michael A Grassi; Jessica M Skeie
Journal:  Mol Vis       Date:  2005-07-14       Impact factor: 2.367

3.  Retinal synthesis and deposition of complement components induced by ocular hypertension.

Authors:  Markus H Kuehn; Chan Y Kim; Jelena Ostojic; Micheal Bellin; Wallace L M Alward; Edwin M Stone; Donald S Sakaguchi; Sinisa D Grozdanic; Young H Kwon
Journal:  Exp Eye Res       Date:  2006-05-04       Impact factor: 3.467

4.  Photoreceptor rosettes in autosomal dominant retinitis pigmentosa with reduced penetrance.

Authors:  W Tulvatana; M Adamian; E L Berson; T P Dryja
Journal:  Arch Ophthalmol       Date:  1999-03

5.  Macular and peripheral distribution of ICAM-1 in the human choriocapillaris and retina.

Authors:  Robert F Mullins; Jessica M Skeie; Elizabeth A Malone; Markus H Kuehn
Journal:  Mol Vis       Date:  2006-03-30       Impact factor: 2.367

6.  Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice.

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Journal:  Cell       Date:  1999-07-09       Impact factor: 41.582

Review 7.  Retinal remodeling during retinal degeneration.

Authors:  Bryan W Jones; Robert E Marc
Journal:  Exp Eye Res       Date:  2005-08       Impact factor: 3.467

8.  A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration.

Authors:  Gregory S Hageman; Don H Anderson; Lincoln V Johnson; Lisa S Hancox; Andrew J Taiber; Lisa I Hardisty; Jill L Hageman; Heather A Stockman; James D Borchardt; Karen M Gehrs; Richard J H Smith; Giuliana Silvestri; Stephen R Russell; Caroline C W Klaver; Irene Barbazetto; Stanley Chang; Lawrence A Yannuzzi; Gaetano R Barile; John C Merriam; R Theodore Smith; Adam K Olsh; Julie Bergeron; Jana Zernant; Joanna E Merriam; Bert Gold; Michael Dean; Rando Allikmets
Journal:  Proc Natl Acad Sci U S A       Date:  2005-05-03       Impact factor: 11.205

9.  Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease.

Authors:  R A Lewis; N F Shroyer; N Singh; R Allikmets; A Hutchinson; Y Li; J R Lupski; M Leppert; M Dean
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

10.  Gene expression analysis of photoreceptor cell loss in bbs4-knockout mice reveals an early stress gene response and photoreceptor cell damage.

Authors:  Ruth E Swiderski; Darryl Y Nishimura; Robert F Mullins; Marissa A Olvera; Jean L Ross; Jian Huang; Edwin M Stone; Val C Sheffield
Journal:  Invest Ophthalmol Vis Sci       Date:  2007-07       Impact factor: 4.799

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1.  Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration.

Authors:  Erin R Burnight; Manav Gupta; Luke A Wiley; Kristin R Anfinson; Audrey Tran; Robinson Triboulet; Jeremy M Hoffmann; Darcey L Klaahsen; Jeaneen L Andorf; Chunhua Jiao; Elliott H Sohn; Malavika K Adur; Jason W Ross; Robert F Mullins; George Q Daley; Thorsten M Schlaeger; Edwin M Stone; Budd A Tucker
Journal:  Mol Ther       Date:  2017-06-12       Impact factor: 11.454

2.  The Rapid-Onset Chorioretinopathy Phenotype of ABCA4 Disease.

Authors:  Koji Tanaka; Winston Lee; Jana Zernant; Kaspar Schuerch; Lyam Ciccone; Stephen H Tsang; Janet R Sparrow; Rando Allikmets
Journal:  Ophthalmology       Date:  2017-09-22       Impact factor: 12.079

Review 3.  CRISPR-Cas9 genome engineering: Treating inherited retinal degeneration.

Authors:  Erin R Burnight; Joseph C Giacalone; Jessica A Cooke; Jessica R Thompson; Laura R Bohrer; Kathleen R Chirco; Arlene V Drack; John H Fingert; Kristan S Worthington; Luke A Wiley; Robert F Mullins; Edwin M Stone; Budd A Tucker
Journal:  Prog Retin Eye Res       Date:  2018-03-22       Impact factor: 21.198

4.  Molecular characterization of foveal versus peripheral human retina by single-cell RNA sequencing.

Authors:  A P Voigt; S S Whitmore; M J Flamme-Wiese; M J Riker; L A Wiley; B A Tucker; E M Stone; R F Mullins; T E Scheetz
Journal:  Exp Eye Res       Date:  2019-05-08       Impact factor: 3.467

5.  Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutations.

Authors:  Wei Chieh Huang; Artur V Cideciyan; Alejandro J Roman; Alexander Sumaroka; Rebecca Sheplock; Sharon B Schwartz; Edwin M Stone; Samuel G Jacobson
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-03-20       Impact factor: 4.799

6.  Vitritis in pediatric genetic retinal disorders.

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Review 7.  Gene therapy for retinal disease.

Authors:  Michelle E McClements; Robert E MacLaren
Journal:  Transl Res       Date:  2013-01-08       Impact factor: 7.012

8.  Psychophysical measurement of rod and cone thresholds in stargardt disease with full-field stimuli.

Authors:  Frederick T Collison; Gerald A Fishman; J Jason McAnany; Jana Zernant; Rando Allikmets
Journal:  Retina       Date:  2014-09       Impact factor: 4.256

9.  Homozygosity mapping guided next generation sequencing to identify the causative genetic variation in inherited retinal degenerative diseases.

Authors:  Srilekha Sundaramurthy; Meenakshi Swaminathan; Parveen Sen; Tharigopala Arokiasamy; Swati Deshpande; Neetha John; Rupali A Gadkari; Ashraf U Mannan; Nagasamy Soumittra
Journal:  J Hum Genet       Date:  2016-07-07       Impact factor: 3.172

10.  HYPERREFLECTIVE DEPOSITION IN THE BACKGROUND OF ADVANCED STARGARDT DISEASE.

Authors:  Lyam Ciccone; Winston Lee; Jana Zernant; Koji Tanaka; Kaspar Schuerch; Stephen H Tsang; Rando Allikmets
Journal:  Retina       Date:  2018-11       Impact factor: 4.256

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