Scientific Article
previous document  unige:89902  next document
add to browser collection

The disulfide isomerase Grp58 is a protective factor against prion neurotoxicity

Hetz, Claudio
Russelakis-Carneiro, Milene
Wälchli, Sébastien
Vial-Knecht, Elisabeth
Maundrell, Kinsey
Castilla, Joaquín
Soto, Claudio
Published in The Journal of neuroscience. 2005, vol. 25, no. 11, p. 2793-2802
Abstract Prion diseases are transmissible neurodegenerative disorders characterized by extensive neuronal apoptosis and accumulation of misfolded prion protein (PrP(SC)). Recent reports indicate that PrP(SC) induces neuronal apoptosis via activation of the endoplasmic reticulum (ER) stress pathway and activation of the ER resident caspase-12. Here, we investigate the relationship between prion replication and induction of ER stress during different stages of the disease in a murine scrapie model. The first alteration observed consists of the upregulation of the ER chaperone of the glucose-regulated protein Grp58, which was detected during the presymptomatic phase and followed closely the formation of PrP(SC). An increase in Grp58 expression correlated with PrP(SC) accumulation at all stages of the disease in different brain areas, suggesting that this chaperone may play an important role in the cellular response to prion infection. Indeed, in vitro studies using N2a neuroblastoma cells demonstrated that inhibition of Grp58 expression with small interfering RNA led to a significant enhancement of PrP(SC) toxicity. Conversely, overexpression of Grp58 protected cells against PrP(SC) toxicity and decreased the rate of caspase-12 activation. Grp58 and PrP were shown to interact by coimmunoprecipitation, observing a higher interaction in cells infected with scrapie prions. Our data indicate that expression of Grp58 is an early cellular response to prion replication, acting as a neuroprotective factor against prion neurotoxicity. Our findings suggest that targeting Grp58 interaction may have applications for developing novel strategies for treatment and early diagnosis of prion diseases.
Keywords Analysis of VarianceAnimalsAnti-Bacterial Agents/pharmacologyBlotting, Western/methodsBrain/metabolism/pathologyCalcimycin/pharmacologyCalcium Signaling/genetics/physiologyCarcinomaCell Line, TumorCell Survival/drug effectsDisease Models, AnimalDose-Response Relationship, DrugElectrophoresis, Polyacrylamide Gel/methodsGene Expression Regulation/drug effects/physiologyHSP70 Heat-Shock Proteins/metabolismHeat-Shock Proteins/genetics/metabolism/therapeutic useHumansImmunohistochemistry/methodsImmunoprecipitation/methodsMembrane Proteins/metabolismMiceMice, Inbred C57BLPhosphopyruvate Hydratase/metabolismPrion Diseases/etiology/prevention & controlPrions/metabolism/pathogenicityProtein Disulfide-Isomerases/genetics/metabolism/therapeutic useRNA, Small Interfering/metabolismTransfection/methods
PMID: 15772339
Full text
Article (Published version) (582 Kb) - document accessible for UNIGE members only Limited access to UNIGE
(ISO format)
HETZ, Claudio et al. The disulfide isomerase Grp58 is a protective factor against prion neurotoxicity. In: The Journal of neuroscience, 2005, vol. 25, n° 11, p. 2793-2802. doi: 10.1523/JNEUROSCI.4090-04.2005

319 hits

0 download


Deposited on : 2016-12-06

Export document
Format :
Citation style :