Literature DB >> 19429590

Cellular origin of fundus autofluorescence in patients and mice with a defective NR2E3 gene.

N-K Wang1, H F Fine, S Chang, C L Chou, W Cella, J Tosi, C-S Lin, T Nagasaki, S H Tsang.   

Abstract

AIM: To characterise new clinical features in a family with enhanced S-cone syndrome (ESCS) and investigate the pathogenesis of these clinical features in the homozygous Nr2e3(rd7) (rd7) mutant mice.
METHODS: Four patients from an affected family were included for genotypic and phenotypic study. Eye tissues from rd7 mice were used to detect a possible relationship between macrophages and autofluorescent material by immunohistochemistry (IHC) staining.
RESULTS: Homozygous mutation in R311Q in NR2E3 was detected in this family. Colour photographs revealed that white dots do not correlate to hyperautofluorescent spots seen in autofluorescence imaging of the macula. OCT showed rosette-like lesions similar to those found in rd7 mice histology sections. From IHC analysis, we observed that F4/80 (a pan macrophage marker) and autofluorescence were colocalised to the same cells within the retina rosettes.
CONCLUSIONS: The retinal structure of a young ESCS patient with homozygous R311Q mutation in the NR2E3 gene is similar to that seen in the rd7 mice. The macrophages were found to contain autofluorescent materials in the retinal rosettes of rd7 mice. These data are consistent with macrophage infiltration contributing to the hyperautofluorescent spots found in our patients.

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Year:  2009        PMID: 19429590      PMCID: PMC2742679          DOI: 10.1136/bjo.2008.153577

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  28 in total

1.  A2E, a lipofuscin fluorophore, in human retinal pigmented epithelial cells in culture.

Authors:  J R Sparrow; C A Parish; M Hashimoto; K Nakanishi
Journal:  Invest Ophthalmol Vis Sci       Date:  1999-11       Impact factor: 4.799

2.  Comparing rod and cone function with fundus autofluorescence images in retinitis pigmentosa.

Authors:  Anthony G Robson; Catherine Egan; Graham E Holder; Alan C Bird; Fred W Fitzke
Journal:  Adv Exp Med Biol       Date:  2003       Impact factor: 2.622

3.  Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.

Authors:  A G Robson; Z Saihan; S A Jenkins; F W Fitzke; A C Bird; A R Webster; G E Holder
Journal:  Br J Ophthalmol       Date:  2006-04       Impact factor: 4.638

4.  DNA damage and repair in light-induced photoreceptor degeneration.

Authors:  William C Gordon; Douglas M Casey; Walter J Lukiw; Nicolas G Bazan
Journal:  Invest Ophthalmol Vis Sci       Date:  2002-11       Impact factor: 4.799

5.  A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse.

Authors:  N B Akhmedov; N I Piriev; B Chang; A L Rapoport; N L Hawes; P M Nishina; S Nusinowitz; J R Heckenlively; T H Roderick; C A Kozak; M Danciger; M T Davisson; D B Farber
Journal:  Proc Natl Acad Sci U S A       Date:  2000-05-09       Impact factor: 11.205

6.  Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice.

Authors:  N B Haider; J K Naggert; P M Nishina
Journal:  Hum Mol Genet       Date:  2001-08-01       Impact factor: 6.150

7.  The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition.

Authors:  S Gerber; J M Rozet; S I Takezawa; L C dos Santos; L Lopes; O Gribouval; C Penet; I Perrault; D Ducroq; E Souied; M Jeanpierre; S Romana; J Frézal; F Ferraz; R Yu-Umesono; A Munnich; J Kaplan
Journal:  Hum Genet       Date:  2000-09       Impact factor: 4.132

8.  The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration.

Authors:  Ann H Milam; Linda Rose; Artur V Cideciyan; Mark R Barakat; Wai-Xing Tang; Nisha Gupta; Tomas S Aleman; Alan F Wright; Edwin M Stone; Val C Sheffield; Samuel G Jacobson
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-02       Impact factor: 11.205

9.  Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome.

Authors:  Alan F Wright; Adam C Reddick; Sharon B Schwartz; Julie S Ferguson; Tomas S Aleman; Ulrich Kellner; Bernhard Jurklies; Andreas Schuster; Eberhart Zrenner; Bernd Wissinger; Alan Lennon; Xinhua Shu; Artur V Cideciyan; Edwin M Stone; Samuel G Jacobson; Anand Swaroop
Journal:  Hum Mutat       Date:  2004-11       Impact factor: 4.878

10.  Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration.

Authors:  Dror Sharon; Michael A Sandberg; Rafael C Caruso; Eliot L Berson; Thaddeus P Dryja
Journal:  Arch Ophthalmol       Date:  2003-09
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  26 in total

1.  Optimization of in vivo confocal autofluorescence imaging of the ocular fundus in mice and its application to models of human retinal degeneration.

Authors:  Peter Charbel Issa; Mandeep S Singh; Daniel M Lipinski; Ngaihang V Chong; François C Delori; Alun R Barnard; Robert E MacLaren
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-02-29       Impact factor: 4.799

Review 2.  Multimodal fundus imaging in fundus albipunctatus with RDH5 mutation: a newly identified compound heterozygous mutation and review of the literature.

Authors:  Nan-Kai Wang; Lan-Hsin Chuang; Chi-Chun Lai; Chai Lin Chou; Hsueh-Yen Chu; Ling Yeung; Yen-Po Chen; Kuan-Jen Chen; Wei-Chi Wu; Tun-Lu Chen; An-Ning Chao; Yih-Shiou Hwang
Journal:  Doc Ophthalmol       Date:  2012-06-06       Impact factor: 2.379

3.  Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse model.

Authors:  Tomas S Aleman; Artur V Cideciyan; Geoffrey K Aguirre; Wei Chieh Huang; Cristina L Mullins; Alejandro J Roman; Alexander Sumaroka; Melani B Olivares; Frank F Tsai; Sharon B Schwartz; Luk H Vandenberghe; Maria P Limberis; Edwin M Stone; Peter Bell; James M Wilson; Samuel G Jacobson
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-08-29       Impact factor: 4.799

4.  CAPN5 mutation in hereditary uveitis: the R243L mutation increases calpain catalytic activity and triggers intraocular inflammation in a mouse model.

Authors:  Katherine J Wert; Alexander G Bassuk; Wen-Hsuan Wu; Lokesh Gakhar; Diana Coglan; MaryAnn Mahajan; Shu Wu; Jing Yang; Chyuan-Sheng Lin; Stephen H Tsang; Vinit B Mahajan
Journal:  Hum Mol Genet       Date:  2015-05-20       Impact factor: 6.150

5.  A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration.

Authors:  Venkata R M Chavali; Naheed W Khan; Catherine A Cukras; Dirk-Uwe Bartsch; Monica M Jablonski; Radha Ayyagari
Journal:  Hum Mol Genet       Date:  2011-02-24       Impact factor: 6.150

6.  Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degeneration.

Authors:  Debarshi Mustafi; Brian M Kevany; Christel Genoud; Kiichiro Okano; Artur V Cideciyan; Alexander Sumaroka; Alejandro J Roman; Samuel G Jacobson; Andreas Engel; Mark D Adams; Krzysztof Palczewski
Journal:  FASEB J       Date:  2011-06-09       Impact factor: 5.191

7.  Novel clinical findings in autosomal recessive NR2E3-related retinal dystrophy.

Authors:  Vittoria Murro; Dario Pasquale Mucciolo; Andrea Sodi; Ilaria Passerini; Dario Giorgio; Gianni Virgili; Stanislao Rizzo
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2018-10-15       Impact factor: 3.117

8.  Bisretinoids mediate light sensitivity resulting in photoreceptor cell degeneration in mice lacking the receptor tyrosine kinase Mer.

Authors:  Jin Zhao; Keiko Ueda; Marina Riera; Hye Jin Kim; Janet R Sparrow
Journal:  J Biol Chem       Date:  2018-10-23       Impact factor: 5.157

9.  Disruption of the human cone photoreceptor mosaic from a defect in NR2E3 transcription factor function in young adults.

Authors:  Sung Pyo Park; In Hwan Hong; Stephen H Tsang; Winston Lee; Jason Horowitz; Suzanne Yzer; Rando Allikmets; Stanley Chang
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2013-04-19       Impact factor: 3.117

10.  Noninvasive, in vivo assessment of mouse retinal structure using optical coherence tomography.

Authors:  M Dominik Fischer; Gesine Huber; Susanne C Beck; Naoyuki Tanimoto; Regine Muehlfriedel; Edda Fahl; Christian Grimm; Andreas Wenzel; Charlotte E Remé; Serge A van de Pavert; Jan Wijnholds; Marek Pacal; Rod Bremner; Mathias W Seeliger
Journal:  PLoS One       Date:  2009-10-19       Impact factor: 3.240

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