Document Detail


A hypothesis on prion disorders: are infectious, inherited, and sporadic causes so distinct?
MedLine Citation:
PMID:  16533656     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Prion diseases include a group of either sporadic, inherited or infectious disorders characterized by spongiform neurodegeneration and reactive glyosis in several brain regions. Whatever the origin, the neuropathological hallmark of prion diseases is the presence of brain aggregates containing an altered isoform of a cellular protein, named prion protein. Recent findings show the potential toxicity of the normal cellular prion protein, which occurs when its physiological metabolism is altered. In particular, several studies demonstrate that accumulation of the prion protein in the cytosol can be a consequence of an increased amount of misfolded prion proteins, a derangement of the correct protein trafficking or a reduced activity of the ubiquitin-proteasome system. The same effects can be a consequence of a mutation in the gene coding for the prion protein. In all these conditions, one assists to accumulation and self-replication of insoluble prion proteins which leads to a severe disease resembling what observed following typical "prion infections". This article provides an opinion aimed at reconciling the classic Prusiner's theory concerning the "prion concepts" with the present knowledge arising from experimental studies on neurodegenerative disorders, suggesting a few overlapping steps in the pathogenesis of these diseases.
Authors:
F Fornai; M Ferrucci; M Gesi; A Bandettini di Poggio; F S Giorgi; F Biagioni; A Paparelli
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Publication Detail:
Type:  Journal Article; Review     Date:  2006-01-04
Journal Detail:
Title:  Brain research bulletin     Volume:  69     ISSN:  0361-9230     ISO Abbreviation:  Brain Res. Bull.     Publication Date:  2006 Mar 
Date Detail:
Created Date:  2006-03-14     Completed Date:  2006-06-01     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  7605818     Medline TA:  Brain Res Bull     Country:  United States    
Other Details:
Languages:  eng     Pagination:  95-100     Citation Subset:  IM    
Affiliation:
Department of Human Morphology and Applied Biology, University of Pisa, via Roma 55, 56126 Pisa, Italy. f.fornai@med.unipi.it
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MeSH Terms
Descriptor/Qualifier:
Brain / metabolism,  pathology,  physiopathology*
Disease Transmission, Infectious
Inclusion Bodies / genetics,  metabolism,  pathology
Models, Neurological
Prion Diseases / genetics,  metabolism,  physiopathology*
Prions / genetics,  metabolism*
Proteasome Endopeptidase Complex / genetics,  metabolism
Protein Folding
Protein Transport / genetics
Ubiquitin / genetics,  metabolism
Chemical
Reg. No./Substance:
0/Prions; 0/Ubiquitin; EC 3.4.25.1/Proteasome Endopeptidase Complex

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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