Literature DB >> 3713985

Retinopathy in mice with experimental scrapie.

J D Foster, H Fraser, M E Bruce.   

Abstract

Scrapie is a naturally occurring neurological disease of adult sheep and goats with an incubation period of several years. Some strains of the causal agent can infect laboratory mice in which the incubation period, as well as the severity and distribution of vacuolar degeneration in the brain, varies according to the strain of the agent and the genotype of the mouse. Retinopathy, involving the partial or complete loss of the photoreceptor layer, was observed in a number of murine scrapie models but was absent in others. The severity of retinopathy depended on both the strain of scrapie and the genotype of mouse used. Some scrapie strains (22C, 87A and 87V) produced minimal or no retinal pathology, others (ME7, 22A and 22L) produced changes in the retinae of only certain mouse genotypes, while the strains 79A and 139A produced degeneration of the photoreceptor layer in every mouse genotype investigated. The severity of retinopathy in the various models did not correlate with the overall intensity of vacuolar degeneration in the brain, with the severity of vacuolation in the centres in the brain controlling pupillary constriction, or with the incubation period.

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Year:  1986        PMID: 3713985     DOI: 10.1111/j.1365-2990.1986.tb00049.x

Source DB:  PubMed          Journal:  Neuropathol Appl Neurobiol        ISSN: 0305-1846            Impact factor:   8.090


  7 in total

1.  Variant CJD and tonometry.

Authors:  J S Mehta; R J Osborne; P A Bloom
Journal:  Br J Ophthalmol       Date:  2004-04       Impact factor: 4.638

2.  Scrapie: Report of an outbreak and brief review.

Authors:  L Petrie; B Heath; D Harold
Journal:  Can Vet J       Date:  1989-04       Impact factor: 1.008

Review 3.  Scrapie pathogenesis in brain and retina: effects of prion protein expression in neurons and astrocytes.

Authors:  Bruce Chesebro; Richard Race; Lisa Kercher
Journal:  J Neurovirol       Date:  2005-10       Impact factor: 2.643

4.  Differences in scrapie-induced pathology of the retina and brain in transgenic mice that express hamster prion protein in neurons, astrocytes, or multiple cell types.

Authors:  Lisa Kercher; Cynthia Favara; Chi-Chao Chan; Richard Race; Bruce Chesebro
Journal:  Am J Pathol       Date:  2004-12       Impact factor: 4.307

5.  A case of Creutzfeldt-Jakob disease related to familial retinitis pigmentosa patients.

Authors:  E Mitrovà
Journal:  Eur J Epidemiol       Date:  1988-03       Impact factor: 8.082

6.  Microglia are not required for prion-induced retinal photoreceptor degeneration.

Authors:  James F Striebel; Brent Race; Katie Williams; James A Carroll; Mikael Klingeborn; Bruce Chesebro
Journal:  Acta Neuropathol Commun       Date:  2019-03-25       Impact factor: 7.801

7.  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

  7 in total

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