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The Role of Autophagy in Age-Related Neurodegeneration
Author(s) -
Brett A. McCray,
J. Paul Taylor
Publication year - 2007
Publication title -
neurosignals
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.755
H-Index - 67
eISSN - 1424-8638
pISSN - 1424-862X
DOI - 10.1159/000109761
Subject(s) - autophagy , neurodegeneration , proteasome , lysosome , ubiquitin , microbiology and biotechnology , biology , protein aggregation , protein degradation , intracellular , catabolism , neuroscience , disease , medicine , biochemistry , gene , apoptosis , metabolism , pathology , enzyme
Most age-related neurodegenerative diseases are characterized by accumulation of aberrant protein aggregates in affected brain regions. In many cases, these proteinaceous deposits are composed of ubiquitin conjugates, suggesting a failure in the clearance of proteins targeted for degradation. The 2 principal routes of intracellular protein catabolism are the ubiquitin proteasome system and the autophagy-lysosome system (autophagy). Both of these degradation pathways have been implicated as playing important roles in the pathogenesis of neurodegenerative disease. Here we describe autophagy and review the evidence suggesting that impairment of autophagy contributes to the initiation or progression of age-related neurodegeneration. We also review recent evidence indicating that autophagy may be exploited to remove toxic protein species, suggesting novel strategies for therapeutic intervention for a class of diseases for which no effective treatments presently exist.

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