Literature DB >> 18157655

Protein quality control in neurodegeneration: walking the tight rope between health and disease.

E M Hol1, W Scheper.   

Abstract

Most neurodegenerative disorders are characterised by deposits of aggregated proteins that are readily visualised by light microscopy. Although the presence of such a bulky structure inside the cell or in the extracellular space is likely not to be healthy, over recent years the idea has emerged that these end-stage aggregates are a relatively safe way to deposit harmful aberrant proteins. Protein quality control is a multi-level security system to safeguard cells from aberrant proteins and is therefore a protective response. However, protein quality control may turn destructive in case of impairment of protein quality control for example by aging or because of overflow of the quality control systems due to prolonged exposure. In many cases the medicine is worse than the cause and the "protective" response of the cell to aggregates kills the cell, rather than the aggregate itself. Here we review the role of protein quality control in neurodegeneration and aim to distinguish protective and destructive responses to aggregates in order to find targets for therapeutic intervention.

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Year:  2007        PMID: 18157655     DOI: 10.1007/s12031-007-0013-8

Source DB:  PubMed          Journal:  J Mol Neurosci        ISSN: 0895-8696            Impact factor:   3.444


  112 in total

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Authors:  Alfred L Goldberg
Journal:  Nature       Date:  2003-12-18       Impact factor: 49.962

Review 2.  Ubiquitin and protein turnover in synapse function.

Authors:  Jason J Yi; Michael D Ehlers
Journal:  Neuron       Date:  2005-09-01       Impact factor: 17.173

Review 3.  Protein quality control in Alzheimer's disease: a fatal saviour.

Authors:  W Scheper; E M Hol
Journal:  Curr Drug Targets CNS Neurol Disord       Date:  2005-06

4.  Activation of the unfolded protein response in Parkinson's disease.

Authors:  J J M Hoozemans; E S van Haastert; P Eikelenboom; R A I de Vos; J M Rozemuller; W Scheper
Journal:  Biochem Biophys Res Commun       Date:  2007-01-17       Impact factor: 3.575

5.  Geldanamycin activates a heat shock response and inhibits huntingtin aggregation in a cell culture model of Huntington's disease.

Authors:  A Sittler; R Lurz; G Lueder; J Priller; H Lehrach; M K Hayer-Hartl; F U Hartl; E E Wanker
Journal:  Hum Mol Genet       Date:  2001-06-01       Impact factor: 6.150

6.  Neuronal dysfunction in a polyglutamine disease model occurs in the absence of ubiquitin-proteasome system impairment and inversely correlates with the degree of nuclear inclusion formation.

Authors:  Aaron B Bowman; Seung-Yun Yoo; Nico P Dantuma; Huda Y Zoghbi
Journal:  Hum Mol Genet       Date:  2005-01-20       Impact factor: 6.150

7.  Proteasomal inhibition by misfolded mutant superoxide dismutase 1 induces selective motor neuron death in familial amyotrophic lateral sclerosis.

Authors:  Makoto Urushitani; Junko Kurisu; Kayoko Tsukita; Ryosuke Takahashi
Journal:  J Neurochem       Date:  2002-12       Impact factor: 5.372

Review 8.  Autophagy in neurodegenerative disease: friend, foe or turncoat?

Authors:  Ralph A Nixon
Journal:  Trends Neurosci       Date:  2006-07-20       Impact factor: 13.837

Review 9.  Pael receptor, endoplasmic reticulum stress, and Parkinson's disease.

Authors:  Ryosuke Takahashi; Yuzuru Imai
Journal:  J Neurol       Date:  2003-10       Impact factor: 4.849

10.  Treatment with arimoclomol, a coinducer of heat shock proteins, delays disease progression in ALS mice.

Authors:  Dairin Kieran; Bernadett Kalmar; James R T Dick; Joanna Riddoch-Contreras; Geoffrey Burnstock; Linda Greensmith
Journal:  Nat Med       Date:  2004-03-21       Impact factor: 53.440

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  7 in total

1.  Apolipoprotein E4 domain interaction induces endoplasmic reticulum stress and impairs astrocyte function.

Authors:  Ning Zhong; Gayathri Ramaswamy; Karl H Weisgraber
Journal:  J Biol Chem       Date:  2009-08-07       Impact factor: 5.157

2.  Oxygen-Glucose Deprivation (OGD) Modulates the Unfolded Protein Response (UPR) and Inflicts Autophagy in a PC12 Hypoxia Cell Line Model.

Authors:  Theofanis Vavilis; Nikoleta Delivanoglou; Eleni Aggelidou; Eleni Stamoula; Kyriakos Mellidis; Aikaterini Kaidoglou; Angeliki Cheva; Chryssa Pourzitaki; Katerina Chatzimeletiou; Antigone Lazou; Maria Albani; Aristeidis Kritis
Journal:  Cell Mol Neurobiol       Date:  2015-08-04       Impact factor: 5.046

3.  Protein aggregation and degradation mechanisms in neurodegenerative diseases.

Authors:  Mari Takalo; Antero Salminen; Hilkka Soininen; Mikko Hiltunen; Annakaisa Haapasalo
Journal:  Am J Neurodegener Dis       Date:  2013-03-08

4.  Proteases inhibition assessment on PC12 and NGF treated cells after oxygen and glucose deprivation reveals a distinct role for aspartyl proteases.

Authors:  Aristidis Kritis; Chryssa Pourzitaki; Ioannis Klagas; Michael Chourdakis; Maria Albani
Journal:  PLoS One       Date:  2011-10-18       Impact factor: 3.240

5.  The yeast ubr1 ubiquitin ligase participates in a prominent pathway that targets cytosolic thermosensitive mutants for degradation.

Authors:  Farzin Khosrow-Khavar; Nancy N Fang; Alex H M Ng; Jason M Winget; Sophie A Comyn; Thibault Mayor
Journal:  G3 (Bethesda)       Date:  2012-05-01       Impact factor: 3.154

6.  Degradation Signals for Ubiquitin-Proteasome Dependent Cytosolic Protein Quality Control (CytoQC) in Yeast.

Authors:  Matthew J Maurer; Eric D Spear; Allen T Yu; Evan J Lee; Saba Shahzad; Susan Michaelis
Journal:  G3 (Bethesda)       Date:  2016-07-07       Impact factor: 3.154

7.  Characterization of CpG island DNA methylation of impairment-related genes in a rat model of cognitive aging.

Authors:  Rebecca P Haberman; Caitlin K Quigley; Michela Gallagher
Journal:  Epigenetics       Date:  2012-08-07       Impact factor: 4.528

  7 in total

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