Document Detail


IRE1 plays an essential role in ER stress-mediated aggregation of mutant huntingtin via the inhibition of autophagy flux.
MedLine Citation:
PMID:  21954231     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Huntington's disease (HD), an inherited neurodegenerative disorder, is caused by an expansion of cytosine-adenine-guanine repeats in the huntingtin gene. The aggregation of mutant huntingtin (mtHTT) and striatal cell loss are representative features to cause uncontrolled movement and cognitive defect in HD. However, underlying mechanism of mtHTT aggregation and cell toxicity remains still elusive. Here, to find new genes modulating mtHTT aggregation, we performed cell-based functional screening using the cDNA expression library and isolated IRE1 gene, one of endoplasmic reticulum (ER) stress sensors. Ectopic expression of IRE1 led to its self-activation and accumulated detergent-resistant mtHTT aggregates. Treatment of neuronal cells with ER stress insults, tunicamycin and thapsigargin, increased mtHTT aggregation via IRE1 activation. The kinase activity of IRE1, but not the endoribonuclease activity, was necessary to stimulate mtHTT aggregation and increased death of neuronal cells, including SH-SY5Y and STHdhQ111/111 huntingtin knock-in striatal cells. Interestingly, ER stress impaired autophagy flux via IRE1-TRAF2 pathway, thus enhancing cellular accumulation of mtHTT. Atg5 deficiency in M5-7 cells increased mtHTT aggregation but blocked ER stress-induced mtHTT aggregation. Further, ER stress markers including p-IRE1 and autophagy markers such as p62 were up-regulated exclusively in the striatal tissues of HD mouse models and in HD patients. Moreover, down-regulation of IRE1 expression rescues the rough-eye phenotype by mtHTT in a HD fly model. These results suggest that IRE1 plays an essential role in ER stress-mediated aggregation of mtHTT via the inhibition of autophagy flux and thus neuronal toxicity of mtHTT aggregates in HD.
Authors:
Huikyong Lee; Jee-Yeon Noh; Yumin Oh; Youngdoo Kim; Jae-Woong Chang; Chul-Woong Chung; Soon-Tae Lee; Manho Kim; Hoon Ryu; Yong-Keun Jung
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2011-09-27
Journal Detail:
Title:  Human molecular genetics     Volume:  21     ISSN:  1460-2083     ISO Abbreviation:  Hum. Mol. Genet.     Publication Date:  2012 Jan 
Date Detail:
Created Date:  2011-12-14     Completed Date:  2012-04-06     Revised Date:  2012-07-11    
Medline Journal Info:
Nlm Unique ID:  9208958     Medline TA:  Hum Mol Genet     Country:  England    
Other Details:
Languages:  eng     Pagination:  101-14     Citation Subset:  IM    
Affiliation:
Global Research Laboratory, School of Biological Science/Bio-MAX Institute, Seoul National University, 599 Gwanak-ro, Gwanak-gu, Seoul 151-742, Korea.
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MeSH Terms
Descriptor/Qualifier:
Animals
Autophagy*
Cell Line
Cells, Cultured
Down-Regulation*
Endoplasmic Reticulum / genetics,  metabolism
Endoplasmic Reticulum Stress*
Endoribonucleases / genetics,  metabolism*
Humans
Huntington Disease / enzymology*,  genetics,  metabolism,  physiopathology*
Membrane Proteins / genetics,  metabolism*
Mice
Mutation
Nerve Tissue Proteins / genetics*,  metabolism*
Neurons / enzymology,  metabolism
Nuclear Proteins / genetics*,  metabolism*
Protein-Serine-Threonine Kinases / genetics,  metabolism*
Rats
Chemical
Reg. No./Substance:
0/HTT protein, human; 0/Membrane Proteins; 0/Nerve Tissue Proteins; 0/Nuclear Proteins; EC 2.7.1.-/ERN2 protein, human; EC 2.7.11.1/Protein-Serine-Threonine Kinases; EC 3.1.-/Endoribonucleases

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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