Aging, protein aggregation, chaperones, and neurodegenerative disorders: mechanisms of coupling and therapeutic opportunities

scientific article published on 31 October 2012

Aging, protein aggregation, chaperones, and neurodegenerative disorders: mechanisms of coupling and therapeutic opportunities is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.5041/RMMJ.10088
P932PMC publication ID3678828
P698PubMed publication ID23908845

P50authorEhud CohenQ37834766
P2860cites workCorrelative Memory Deficits, Abeta Elevation, and Amyloid Plaques in Transgenic MiceQ22242267
A mutation in APP protects against Alzheimer’s disease and age-related cognitive declineQ22251083
Amyloid-beta protein dimers isolated directly from Alzheimer's brains impair synaptic plasticity and memoryQ24645499
Association of FOXO3A variation with human longevity confirmed in German centenariansQ24646035
FOXO3A genotype is strongly associated with human longevityQ24647408
TDP-1/TDP-43 regulates stress signaling and age-dependent proteotoxicity in Caenorhabditis elegansQ27332459
Genes that act downstream of DAF-16 to influence the lifespan of Caenorhabditis elegansQ27860971
A C. elegans mutant that lives twice as long as wild typeQ27861054
Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer's amyloid beta-peptideQ28131750
Adapting proteostasis for disease interventionQ28131818
Huntingtin aggregation and toxicity in Huntington's diseaseQ28204163
Evidence for lifespan extension and delayed age-related biomarkers in insulin receptor substrate 1 null miceQ28252794
Deletion of Irs2 reduces amyloid deposition and rescues behavioural deficits in APP transgenic miceQ28505715
Lysosomal proteolysis and autophagy require presenilin 1 and are disrupted by Alzheimer-related PS1 mutationsQ28506710
daf-2, an insulin receptor-like gene that regulates longevity and diapause in Caenorhabditis elegansQ28611331
Daf-2 signaling modifies mutant SOD1 toxicity in C. elegansQ28731030
Molecular chaperones in protein folding and proteostasisQ29547715
Extended longevity in mice lacking the insulin receptor in adipose tissueQ29614549
The IRS2 Gly1057Asp variant is associated with human longevity.Q54456152
Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneityQ70142305
Alzheimer's diseaseQ84113248
A systematic RNAi screen identifies a critical role for mitochondria in C. elegans longevityQ29614550
Autophagy gone awry in neurodegenerative diseasesQ29614849
TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosisQ29615597
IGF-1 receptor regulates lifespan and resistance to oxidative stress in miceQ29616382
The plasticity of aging: insights from long-lived mutantsQ29616584
Direct inhibition of the longevity-promoting factor SKN-1 by insulin-like signaling in C. elegansQ29619580
Opposing activities protect against age-onset proteotoxicityQ29619758
Regulation of Aging and Age-Related Disease by DAF-16 and Heat-Shock FactorQ29619759
The threshold for polyglutamine-expansion protein aggregation and cellular toxicity is dynamic and influenced by aging in Caenorhabditis elegansQ29619760
The effect of retarded growth upon the length of life span and upon the ultimate body size. 1935Q29620325
Dietary restriction suppresses proteotoxicity and enhances longevity by an hsf-1-dependent mechanism in Caenorhabditis elegansQ30488783
Reduced IGF-1 signaling delays age-associated proteotoxicity in miceQ30497845
Neuron-specific proteotoxicity of mutant ataxin-3 in C. elegans: rescue by the DAF-16 and HSF-1 pathwaysQ30502208
Expression of human beta-amyloid peptide in transgenic Caenorhabditis elegansQ33902367
Small heat shock proteins potentiate amyloid dissolution by protein disaggregases from yeast and humansQ34313725
Amyloid beta-protein dimers rapidly form stable synaptotoxic protofibrilsQ34330681
Early-onset behavioral and synaptic deficits in a mouse model of Alzheimer's diseaseQ34460984
Functionally significant insulin-like growth factor I receptor mutations in centenariansQ34757952
TDP-43 neurotoxicity and protein aggregation modulated by heat shock factor and insulin/IGF-1 signalingQ34829446
The mechanism of γ-Secretase dysfunction in familial Alzheimer diseaseQ36000134
Lysosomal calcium homeostasis defects, not proton pump defects, cause endo-lysosomal dysfunction in PSEN-deficient cells.Q36085273
The ubiquitin proteolytic system: from a vague idea, through basic mechanisms, and onto human diseases and drug targetingQ36375898
Mechanisms of Parkinson's disease linked to pathological alpha-synuclein: new targets for drug discoveryQ36610346
HSF-1 regulators DDL-1/2 link insulin-like signaling to heat-shock responses and modulation of longevityQ36737237
Aging and survival: the genetics of life span extension by dietary restriction.Q37121798
FOXO3a is broadly neuroprotective in vitro and in vivo against insults implicated in motor neuron diseasesQ37356513
A kinetic assessment of the C. elegans amyloid disaggregation activity enables uncoupling of disassembly and proteolysisQ39953074
Mutations of the presenilin I gene in families with early-onset Alzheimer's diseaseQ41263613
Temporal requirements of insulin/IGF-1 signaling for proteotoxicity protectionQ41769831
Temporal requirements of heat shock factor-1 for longevity assuranceQ43175674
Mitochondrial electron transport is a key determinant of life span in Caenorhabditis elegansQ43799857
Rates of behavior and aging specified by mitochondrial function during developmentQ44242015
Hsp104 catalyzes formation and elimination of self-replicating Sup35 prion conformersQ44904974
Neuronal IGF-1 resistance reduces Abeta accumulation and protects against premature death in a model of Alzheimer's disease.Q45987250
Regulation of C. elegans DAF-16 and its human ortholog FKHRL1 by the daf-2 insulin-like signaling pathwayQ46102898
Conformational diseaseQ46332791
Impaired spatial learning in the APPSwe + PSEN1DeltaE9 bigenic mouse model of Alzheimer's disease.Q48306292
Co-expression of multiple transgenes in mouse CNS: a comparison of strategiesQ48889458
Chaperonin TRiC promotes the assembly of polyQ expansion proteins into nontoxic oligomers.Q50715387
Aging as a major risk for degenerative diseases of the central nervous system.Q53314938
P433issue4
P407language of work or nameEnglishQ1860
P921main subjectneurodegenerationQ1755122
protein aggregationQ7251455
molecular chaperonesQ422496
P304page(s)e0021
P577publication date2012-10-31
P1433published inRambam Maimonides Medical JournalQ18209815
P1476titleAging, protein aggregation, chaperones, and neurodegenerative disorders: mechanisms of coupling and therapeutic opportunities
P478volume3

Reverse relations

cites work (P2860)
Q53355168Amyloid-beta (Aβ₁₋₄₂)-induced paralysis in Caenorhabditis elegans is inhibited by the polyphenol quercetin through activation of protein degradation pathways.
Q38382516Autoimmune Responses to Soluble Aggregates of Amyloidogenic Proteins Involved in Neurodegenerative Diseases: Overlapping Aggregation Prone and Autoimmunogenic regions
Q31068168CPAD, Curated Protein Aggregation Database: A Repository of Manually Curated Experimental Data on Protein and Peptide Aggregation
Q33824789Characterizing the altered cellular proteome induced by the stress-independent activation of heat shock factor 1.
Q42113553Imperfect asymmetry: The mechanism governing asymmetric partitioning of damaged cellular components during mitosis
Q40882330Somatic expression of unc-54 and vha-6 mRNAs declines but not pan-neuronal rgef-1 and unc-119 expression in aging Caenorhabditis elegans