| Literature DB >> 30116051 |
Barry Boland1, Wai Haung Yu2, Olga Corti3, Bertrand Mollereau4, Alexandre Henriques5, Erwan Bezard6, Greg M Pastores7, David C Rubinsztein8, Ralph A Nixon9,10, Michael R Duchen11, Giovanna R Mallucci12, Guido Kroemer13,14,15,16,17,18,19, Beth Levine20,21, Eeva-Liisa Eskelinen22, Fanny Mochel23, Michael Spedding24, Caroline Louis25, Olivier R Martin26, Mark J Millan25.
Abstract
Neurodegenerative disorders of ageing (NDAs) such as Alzheimer disease, Parkinson disease, frontotemporal dementia, Huntington disease and amyotrophic lateral sclerosis represent a major socio-economic challenge in view of their high prevalence yet poor treatment. They are often called 'proteinopathies' owing to the presence of misfolded and aggregated proteins that lose their physiological roles and acquire neurotoxic properties. One reason underlying the accumulation and spread of oligomeric forms of neurotoxic proteins is insufficient clearance by the autophagic-lysosomal network. Several other clearance pathways are also compromised in NDAs: chaperone-mediated autophagy, the ubiquitin-proteasome system, extracellular clearance by proteases and extrusion into the circulation via the blood-brain barrier and glymphatic system. This article focuses on emerging mechanisms for promoting the clearance of neurotoxic proteins, a strategy that may curtail the onset and slow the progression of NDAs.Entities:
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Year: 2018 PMID: 30116051 PMCID: PMC6456907 DOI: 10.1038/nrd.2018.109
Source DB: PubMed Journal: Nat Rev Drug Discov ISSN: 1474-1776 Impact factor: 84.694