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Immunoreactivity to Lys63-linked polyubiquitin is a feature of neurodegeneration

Authors :
James Lowe
Simon M. L. Paine
Lynn Bedford
Paul W. Sheppard
R. John Mayer
Julian R. Thorpe
James R. Cavey
Robert Layfield
Nin Bajaj
Source :
Neuroscience Letters. 460:205-208
Publication Year :
2009
Publisher :
Elsevier BV, 2009.

Abstract

The major human neurodegenerative diseases are characterised by ubiquitin-positive intraneuronal inclusions, however the precise nature of the ubiquitin modifications in these structures is unclear. Using a monoclonal antibody specific for Lys63-linked polyubiquitin we have performed the first immunohistochemical analysis of linkage-specific ubiquitination in vivo associated with neurodegeneration. Immunoreactivity was detected within the pathological lesions of Alzheimer's, Huntington's and Parkinson's disease brains, although staining of Lewy bodies in the substantia nigra in Parkinson's disease was rare, indicating a selective involvement of Lys63-linked polyubiquitin in inclusion biogenesis in this disorder. Immunoreactivity was also a feature in neurons of proteasome-depleted mice, suggesting a proteasomal contribution to the degradation of Lys63-linked polyubiquitinated proteins in vivo.

Details

ISSN :
03043940
Volume :
460
Database :
OpenAIRE
Journal :
Neuroscience Letters
Accession number :
edsair.doi.dedup.....6c79617f40c294e8fead531a5c9a46e5
Full Text :
https://doi.org/10.1016/j.neulet.2009.05.074