Literature DB >> 21400062

Temporal and spatial characteristics of cone degeneration in RCS rats.

Yan Ming Huang1, Zheng Qin Yin, Kang Liu, Shu Jia Huo.   

Abstract

PURPOSE: The temporal and spatial characteristics of cone degeneration in the Royal College of Surgeons (RCS) rat were studied to provide information for treatment strategies of retinitis pigmentosa.
METHODS: Nonpigmented dystrophic RCS rats (RCS) and pigmented nondystrophic RCS rats (controls) were used. Cone processes were visualized with peanut agglutinin (PNA).
RESULTS: Cone development appears to have been completed by postnatal day 21 (P21) in both the RCS and control rats. Signs of cone degeneration were obvious by P30, with shorter outer segments (OSs) and enlarged inner segments (ISs). At that time, 81.7% of the cones retained stained ISs. The rate of IS density decline was slower in the peripheral, nasal, and superior retina, and only 43.6% of the cones with ISs were present at P45. By P60, PNA-labeled cone ISs were distorted and restricted to the peripheral retina, and by P90, few cone pedicles were detected.
CONCLUSIONS: Our findings indicate that therapeutic strategies aimed at rescuing cones in the degenerating retina should be applied before P21 and no later than P45 while substantial numbers of cones retain their ISs. Either the middle or peripheral regions of the nasal and superior retina are the best locations for transplantation strategies.

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Year:  2011        PMID: 21400062     DOI: 10.1007/s10384-010-0908-8

Source DB:  PubMed          Journal:  Jpn J Ophthalmol        ISSN: 0021-5155            Impact factor:   2.447


  37 in total

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Journal:  Ophthalmic Res       Date:  1997       Impact factor: 2.892

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4.  Subretinal transplantation of brain-derived precursor cells to young RCS rats promotes photoreceptor cell survival.

Authors:  Anita Blixt Wojciechowski; Ulrica Englund; Cecilia Lundberg; Klas Wictorin; Karin Warfvinge
Journal:  Exp Eye Res       Date:  2002-07       Impact factor: 3.467

5.  Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa.

Authors:  M E McLaughlin; M A Sandberg; E L Berson; T P Dryja
Journal:  Nat Genet       Date:  1993-06       Impact factor: 38.330

6.  Migration and synaptogenesis of cone photoreceptors in the developing mouse retina.

Authors:  K A Rich; Y Zhan; J C Blanks
Journal:  J Comp Neurol       Date:  1997-11-10       Impact factor: 3.215

7.  Rat bone marrow stromal cells express retinal phenotypic markers following different induction protocols.

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8.  Identification and characterization of rod-derived cone viability factor.

Authors:  Thierry Léveillard; Saddek Mohand-Saïd; Olivier Lorentz; David Hicks; Anne-Claire Fintz; Emmanuelle Clérin; Manuel Simonutti; Valérie Forster; Nükhet Cavusoglu; Frédéric Chalmel; Pascal Dollé; Olivier Poch; George Lambrou; José-Alain Sahel
Journal:  Nat Genet       Date:  2004-06-27       Impact factor: 38.330

9.  Optimal conditions for long-term photoreceptor cell rescue in RCS rats: the necessity for healthy RPE transplants.

Authors:  L Li; J E Turner
Journal:  Exp Eye Res       Date:  1991-06       Impact factor: 3.467

Review 10.  Neural remodeling in retinal degeneration.

Authors:  Robert E Marc; Bryan W Jones; Carl B Watt; Enrica Strettoi
Journal:  Prog Retin Eye Res       Date:  2003-09       Impact factor: 21.198

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2.  M-opsin protein degradation is inhibited by MG-132 in Rpe65⁻/⁻ retinal explant culture.

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3.  Early Events in Retinal Degeneration Caused by Rhodopsin Mutation or Pigment Epithelium Malfunction: Differences and Similarities.

Authors:  Johnny Di Pierdomenico; Diego García-Ayuso; Isabel Pinilla; Nicolás Cuenca; Manuel Vidal-Sanz; Marta Agudo-Barriuso; María P Villegas-Pérez
Journal:  Front Neuroanat       Date:  2017-03-06       Impact factor: 3.856

Review 4.  In vivo retinal imaging in translational regenerative research.

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Journal:  Ann Transl Med       Date:  2020-09

5.  Beyond Sector Retinitis Pigmentosa: Expanding the Phenotype and Natural History of the Rhodopsin Gene Codon 106 Mutation (Gly-to-Arg) in Autosomal Dominant Retinitis Pigmentosa.

Authors:  Brian G Ballios; Emily M Place; Luis Martinez-Velazquez; Eric A Pierce; Jason I Comander; Rachel M Huckfeldt
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