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Prions and prion diseases: Insights from the eye.
Singh, Neena; Chaudhary, Suman; Ashok, Ajay; Lindner, Ewald.
Afiliación
  • Singh N; Departments of Pathology, School of Medicine, Case Western Reserve University, Cleveland, OH, 44106, USA. Electronic address: neena.singh@case.edu.
  • Chaudhary S; Departments of Pathology, School of Medicine, Case Western Reserve University, Cleveland, OH, 44106, USA.
  • Ashok A; Departments of Pathology, School of Medicine, Case Western Reserve University, Cleveland, OH, 44106, USA.
  • Lindner E; Department of Ophthalmology, Medical University of Graz, Auenbruggerplatz 4, 8036, Graz, Austria.
Exp Eye Res ; 199: 108200, 2020 10.
Article en En | MEDLINE | ID: mdl-32858007
ABSTRACT
Prion diseases are invariably fatal neurodegenerative disorders that have gained much publicity due to their transmissible nature. Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common human prion disorder, with an incidence of 1 in a million. Inherited prion disorders are relatively rare, and associated with mutations in the prion protein gene. More than 50 different point mutations, deletions, and insertions have been identified so far. Most are autosomal dominant and fully penetrant. Prion disorders also occur in animals, and are of major concern because of the potential for spreading to humans. The principal pathogenic event underlying all prion disorders is a change in the conformation of prion protein (PrPC) from a mainly α-helical to a ß-sheet rich isoform, PrP-scrapie (PrPSc). Accumulation of PrPSc in the brain parenchyma is the major cause of neuronal degeneration. The mechanism by which PrPSc is transmitted, propagates, and causes neurodegenerative changes has been investigated over the years, and several clues have emerged. Efforts are also ongoing for identifying specific and sensitive diagnostic tests for sCJD and animal prion disorders, but success has been limited. The eye is suitable for these evaluations because it shares several anatomical and physiological features with the brain, and can be observed in vivo during disease progression. The retina, considered an extension of the central nervous system, is involved extensively in prion disorders. Accordingly, Optical Coherence Tomography and electroretinogram have shown some promise as pre-mortem diagnostic tests for human and animal prion disorders. However, a complete understanding of the physiology of PrPC and pathobiology of PrPSc in the eye is essential for developing specific and sensitive tests. Below, we summarize recent progress in ocular physiology and pathology in prion disorders, and the eye as an anatomically accessible site to diagnose, monitor disease progression, and test therapeutic options.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Priones / Regulación de la Expresión Génica / Segmento Anterior del Ojo Límite: Animals / Humans Idioma: En Revista: Exp Eye Res Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Priones / Regulación de la Expresión Génica / Segmento Anterior del Ojo Límite: Animals / Humans Idioma: En Revista: Exp Eye Res Año: 2020 Tipo del documento: Article