BimEL as a possible molecular link between proteasome dysfunction and cell death induced by mutant huntingtin

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BimEL as a possible molecular link between proteasome dysfunction and cell death induced by mutant huntingtin is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1111/J.1460-9568.2010.07215.X
P8608Fatcat IDrelease_jd4v6tnb7ndsth6n4ekcbnmota
P932PMC publication ID2931320
P698PubMed publication ID20497470
P5875ResearchGate publication ID44625541

P2093author name stringJianning Wei
Mark McCollum
Nithya Bhagavatula
Onome Ulukpo
Rebecca Leon
P2860cites workBH3-only proteins Bid and Bim(EL) are differentially involved in neuronal dysfunction in mouse models of Huntington's diseaseQ45304659
Global changes to the ubiquitin system in Huntington's disease.Q45305824
Cytoplasmic inclusions of Htt exon1 containing an expanded polyglutamine tract suppress execution of apoptosis in sympathetic neurons.Q46178162
Bim is elevated in Alzheimer's disease neurons and is required for beta-amyloid-induced neuronal apoptosis.Q48298601
PARP cleavage as a means of assessing apoptosisQ79317596
Regulatory phosphorylation of Bim: sorting out the ERK from the JNKQ81833475
ASK1 is essential for endoplasmic reticulum stress-induced neuronal cell death triggered by expanded polyglutamine repeatsQ24298956
Bid, a Bcl2 Interacting Protein, Mediates Cytochrome c Release from Mitochondria in Response to Activation of Cell Surface Death ReceptorsQ24310559
Cleavage of BID by caspase 8 mediates the mitochondrial damage in the Fas pathway of apoptosisQ24310597
Polyglutamine expansion of huntingtin impairs its nuclear exportQ24338269
JNK phosphorylation of Bim-related members of the Bcl2 family induces Bax-dependent apoptosisQ24554008
Characterization of the c-Jun N-terminal kinase-BimEL signaling pathway in neuronal apoptosis.Q27919665
The proapoptotic activity of the Bcl-2 family member Bim is regulated by interaction with the dynein motor complexQ28141249
Induction of BIM, a proapoptotic BH3-only BCL-2 family member, is critical for neuronal apoptosisQ28212224
Bid-deficient mice are resistant to Fas-induced hepatocellular apoptosisQ28511080
Amino-terminal fragments of mutant huntingtin show selective accumulation in striatal neurons and synaptic toxicityQ28513938
Impairment of the ubiquitin-proteasome system by protein aggregationQ29614556
ER stress triggers apoptosis by activating BH3-only protein BimQ29617730
Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brainQ29617982
Increased susceptibility of cytoplasmic over nuclear polyglutamine aggregates to autophagic degradationQ33947993
BH3-Only proteins-essential initiators of apoptotic cell deathQ34117362
Failure of the ubiquitin-proteasome system in Parkinson's diseaseQ34325371
Mutant huntingtin alters MAPK signaling pathways in PC12 and striatal cells: ERK1/2 protects against mutant huntingtin-associated toxicity.Q34473189
Apoptosis in Huntington's disease.Q35092246
Nonapoptotic neurodegeneration in a transgenic mouse model of Huntington's diseaseQ35176635
The proapoptotic BH3-only protein bim is expressed in hematopoietic, epithelial, neuronal, and germ cellsQ35745742
Two molecular pathways initiate mitochondria-dependent dopaminergic neurodegeneration in experimental Parkinson's diseaseQ35808960
Impaired ubiquitin-proteasome system activity in the synapses of Huntington's disease miceQ36534628
Multisite phosphorylation regulates Bim stability and apoptotic activityQ36756298
Aggregation of huntingtin in yeast varies with the length of the polyglutamine expansion and the expression of chaperone proteinsQ37109961
Inhibition of the ubiquitin-proteasome system in Alzheimer's disease.Q37387675
Increased expression of Bim contributes to the potentiation of serum deprivation-induced apoptotic cell death in Huntington's disease knock-in striatal cell lineQ39952286
Global impairment of the ubiquitin-proteasome system by nuclear or cytoplasmic protein aggregates precedes inclusion body formation.Q40461698
Extracellular signal-regulated kinases 1/2 are serum-stimulated "Bim(EL) kinases" that bind to the BH3-only protein Bim(EL) causing its phosphorylation and turnoverQ40606380
Phosphorylation of Bim-EL by Erk1/2 on serine 69 promotes its degradation via the proteasome pathway and regulates its proapoptotic function.Q40626751
Altered proteasomal function due to the expression of polyglutamine-expanded truncated N-terminal huntingtin induces apoptosis by caspase activation through mitochondrial cytochrome c releaseQ40808988
Intranuclear huntingtin increases the expression of caspase-1 and induces apoptosisQ40840397
Importance of poly(ADP-ribose) polymerase and its cleavage in apoptosis. Lesson from an uncleavable mutantQ40990869
Intraneuronal aggregate formation and cell death after viral expression of expanded polyglutamine tracts in the adult rat brain.Q41713142
Endoplasmic reticulum stress and alteration in calcium homeostasis are involved in cadmium-induced apoptosisQ42827151
FOXO transcription factors directly activate bim gene expression and promote apoptosis in sympathetic neuronsQ42918105
Aggregate formation inhibits proteasomal degradation of polyglutamine proteins.Q44175807
JNK-mediated BIM phosphorylation potentiates BAX-dependent apoptosisQ44485247
Neuronal induction of the immunoproteasome in Huntington's disease.Q44699105
Sequential activation of individual caspases, and of alterations in Bcl‐2 proapoptotic signals in a mouse model of Huntington's diseaseQ45291644
Accumulation of aberrant ubiquitin induces aggregate formation and cell death in polyglutamine diseasesQ45293883
Proteasome impairment does not contribute to pathogenesis in R6/2 Huntington's disease mice: exclusion of proteasome activator REGgamma as a therapeutic targetQ45299199
P433issue11
P407language of work or nameEnglishQ1860
P921main subjectcell deathQ2383867
P304page(s)1915-1925
P577publication date2010-05-24
P1433published inEuropean Journal of NeuroscienceQ5412733
P1476titleBimEL as a possible molecular link between proteasome dysfunction and cell death induced by mutant huntingtin
P478volume31

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cites work (P2860)
Q47288108Aberrant subcellular localization of SQSTM1/p62 contributes to increased vulnerability to proteotoxic stress recovery in Huntington's disease
Q45289973Bcl-2/adenovirus E1B 19-kDa interacting protein (BNip3) has a key role in the mitochondrial dysfunction induced by mutant huntingtin.
Q38818046Bim gene dosage is critical in modulating nephron progenitor survival in the absence of microRNAs during kidney development
Q37527207Caspase-2 is essential for c-Jun transcriptional activation and Bim induction in neuron death.
Q58994518Crosstalk between Endoplasmic Reticulum Stress and Protein Misfolding in Neurodegenerative Diseases
Q26822846Defining the role of the Bcl-2 family proteins in Huntington's disease
Q36283269Palmitoylation and trafficking of GAD65 are impaired in a cellular model of Huntington's disease
Q37930038Pathogenic Mechanisms in Huntington's Disease
Q26781203Regulation of Bim in Health and Disease
Q58801228The Parkinson's disease gene product DJ-1 modulates miR-221 to promote neuronal survival against oxidative stress
Q26771343The Unfolded Protein Response and the Role of Protein Disulfide Isomerase in Neurodegeneration

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