Literature DB >> 16113366

Abnormal prion protein in the retina of the most commonly occurring subtype of sporadic Creutzfeldt-Jakob disease.

M W Head1, A H Peden, H M Yull, D L Ritchie, R E Bonshek, A B Tullo, J W Ironside.   

Abstract

BACKGROUND: Involvement of the eye has been reported in patients with variant Creutzfeldt-Jakob disease (vCJD), but there is disagreement on whether retinal involvement occurs in sporadic Creutzfeldt-Jakob disease (sCJD).
METHODS: Western blotting, paraffin embedded tissue blotting, and immunohistochemistry were used to test whether the abnormal form of the prion protein (PrPSc) accumulates to detectable levels in the eye in a case of the most common subtype of sCJD (MM1).
RESULTS: Low levels of PrPSc were detectable in the retina, localised to the plexiform layers of the central retina. PrPSc was not detectable in other ocular tissues.
CONCLUSIONS: The abnormal form of the prion protein is present in the retina in the most common sCJD subtype (MM1), albeit at levels lower than those found previously in vCJD and in sCJD of the VV2 subtype.

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Year:  2005        PMID: 16113366      PMCID: PMC1772846          DOI: 10.1136/bjo.2004.063495

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


  13 in total

1.  Extraneural pathologic prion protein.

Authors:  Alexandre Favereaux; Armand Perret-Liaudet; Anne Vital
Journal:  N Engl J Med       Date:  2004-02-12       Impact factor: 91.245

2.  Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay.

Authors:  J D Wadsworth; S Joiner; A F Hill; T A Campbell; M Desbruslais; P J Luthert; J Collinge
Journal:  Lancet       Date:  2001-07-21       Impact factor: 79.321

3.  Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.

Authors:  P Parchi; A Giese; S Capellari; P Brown; W Schulz-Schaeffer; O Windl; I Zerr; H Budka; N Kopp; P Piccardo; S Poser; A Rojiani; N Streichemberger; J Julien; C Vital; B Ghetti; P Gambetti; H Kretzschmar
Journal:  Ann Neurol       Date:  1999-08       Impact factor: 10.422

Review 4.  Iatrogenic Creutzfeldt-Jakob disease at the millennium.

Authors:  P Brown; M Preece; J P Brandel; T Sato; L McShane; I Zerr; A Fletcher; R G Will; M Pocchiari; N R Cashman; J H d'Aignaux; L Cervenáková; J Fradkin; L B Schonberger; S J Collins
Journal:  Neurology       Date:  2000-10-24       Impact factor: 9.910

5.  Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion.

Authors:  C A Llewelyn; P E Hewitt; R S G Knight; K Amar; S Cousens; J Mackenzie; R G Will
Journal:  Lancet       Date:  2004-02-07       Impact factor: 79.321

6.  Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies.

Authors:  M Pocchiari; M Puopolo; E A Croes; H Budka; E Gelpi; S Collins; V Lewis; T Sutcliffe; A Guilivi; N Delasnerie-Laupretre; J-P Brandel; A Alperovitch; I Zerr; S Poser; H A Kretzschmar; A Ladogana; I Rietvald; E Mitrova; P Martinez-Martin; J de Pedro-Cuesta; M Glatzel; A Aguzzi; S Cooper; J Mackenzie; C M van Duijn; R G Will
Journal:  Brain       Date:  2004-09-10       Impact factor: 13.501

7.  Advances in the detection of prion protein in peripheral tissues of variant Creutzfeldt-Jakob disease patients using paraffin-embedded tissue blotting.

Authors:  D L Ritchie; M W Head; J W Ironside
Journal:  Neuropathol Appl Neurobiol       Date:  2004-08       Impact factor: 8.090

8.  Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient.

Authors:  Alexander H Peden; Mark W Head; Diane L Ritchie; Jeanne E Bell; James W Ironside
Journal:  Lancet       Date:  2004 Aug 7-13       Impact factor: 79.321

9.  Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study.

Authors:  Mark W Head; Diane Ritchie; Nadine Smith; Victoria McLoughlin; William Nailon; Sazia Samad; Stephen Masson; Matthew Bishop; Linda McCardle; James W Ironside
Journal:  Am J Pathol       Date:  2004-01       Impact factor: 4.307

10.  Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease.

Authors:  Mark W Head; Victoria Northcott; Kathleen Rennison; Diane Ritchie; Linda McCardle; Tristan J R Bunn; Neil F McLennan; James W Ironside; Andrew B Tullo; Richard E Bonshek
Journal:  Invest Ophthalmol Vis Sci       Date:  2003-01       Impact factor: 4.799

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  10 in total

1.  Temporal Resolution of Misfolded Prion Protein Transport, Accumulation, Glial Activation, and Neuronal Death in the Retinas of Mice Inoculated with Scrapie.

Authors:  M Heather West Greenlee; Melissa Lind; Robyn Kokemuller; Najiba Mammadova; Naveen Kondru; Sireesha Manne; Jodi Smith; Anumantha Kanthasamy; Justin Greenlee
Journal:  Am J Pathol       Date:  2016-08-09       Impact factor: 4.307

2.  Ophthalmic surgery in prion diseases.

Authors:  Tsuyoshi Hamaguchi; Moeko Noguchi-Shinohara; Yosikazu Nakamura; Takeshi Sato; Tetsuyuki Kitamoto; Hidehiro Mizusawa; Masahito Yamada
Journal:  Emerg Infect Dis       Date:  2007-01       Impact factor: 6.883

3.  The toxicity of the PrP106-126 prion peptide on cultured photoreceptors correlates with the prion protein distribution in the mammalian and human retina.

Authors:  Jie Gong; Abdeljelil Jellali; Valérie Forster; Jérôme Mutterer; Elisabeth Dubus; Wilko D Altrock; José A Sahel; Alvaro Rendon; Serge Picaud
Journal:  Am J Pathol       Date:  2007-04       Impact factor: 4.307

4.  Clinical, electroretinographic and histomorphometric evaluation of the retina in sheep with natural scrapie.

Authors:  Alain Regnier; Olivier Andreoletti; Olivier Albaric; Delphine Cayez Gruson; François Schelcher; Pierre-Louis Toutain
Journal:  BMC Vet Res       Date:  2011-06-06       Impact factor: 2.741

5.  PrPres deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD).

Authors:  Masaki Takao; Hiroaki Kimura; Tetsuyuki Kitamoto; Ban Mihara
Journal:  Acta Neuropathol Commun       Date:  2018-08-10       Impact factor: 7.801

6.  Prion-induced photoreceptor degeneration begins with misfolded prion protein accumulation in cones at two distinct sites: cilia and ribbon synapses.

Authors:  James F Striebel; Brent Race; Jacqueline M Leung; Cindi Schwartz; Bruce Chesebro
Journal:  Acta Neuropathol Commun       Date:  2021-01-29       Impact factor: 7.801

Review 7.  Differential Accumulation of Misfolded Prion Strains in Natural Hosts of Prion Diseases.

Authors:  Zoe J Lambert; Justin J Greenlee; Eric D Cassmann; M Heather West Greenlee
Journal:  Viruses       Date:  2021-12-07       Impact factor: 5.048

8.  Prion protein facilitates retinal iron uptake and is cleaved at the β-site: Implications for retinal iron homeostasis in prion disorders.

Authors:  Abhishek Asthana; Shounak Baksi; Ajay Ashok; Shilpita Karmakar; Najiba Mammadova; Robyn Kokemuller; Mary Heather Greenlee; Qingzhong Kong; Neena Singh
Journal:  Sci Rep       Date:  2017-08-29       Impact factor: 4.379

9.  Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease Patients.

Authors:  Christina D Orrù; Katrin Soldau; Christian Cordano; Jorge Llibre-Guerra; Ari J Green; Henry Sanchez; Bradley R Groveman; Steven D Edland; Jiri G Safar; Jonathan H Lin; Byron Caughey; Michael D Geschwind; Christina J Sigurdson
Journal:  mBio       Date:  2018-11-20       Impact factor: 7.867

10.  A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis.

Authors:  Penny J Norsworthy; Andrew G B Thompson; Tze H Mok; Fernando Guntoro; Luke C Dabin; Akin Nihat; Ross W Paterson; Jonathan M Schott; John Collinge; Simon Mead; Emmanuelle A Viré
Journal:  Nat Commun       Date:  2020-08-07       Impact factor: 14.919

  10 in total

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