Mitochondrial fission and cristae disruption increase the response of cell models of Huntington's disease to apoptotic stimuli (Q34605764)

3 August 2017

Mitochondrial fission and cristae disruption increase the response of cell models of Huntington's disease to apoptotic stimuli (English)

1 reference

3 August 2017

0 references

0 references

mitochondrial fission

1 reference

Raffaele Lopreiato

4

0 references

Marta Giacomello

Marta Giacomello

2

0 references

Luca Scorrano

Luca Scorrano

10

0 references

Walter Malorni

Walter Malorni

7

0 references

Ernesto Carafoli

Ernesto Carafoli

9

0 references

author name string

Veronica Costa

1

1 reference

3 August 2017

Roman Hudec

3

1 reference

3 August 2017

Gennady Ermak

5

1 reference

3 August 2017

Dmitri Lim

6

1 reference

3 August 2017

Kelvin J A Davies

8

1 reference

3 August 2017

language of work or name

1 reference

1 December 2010

1 reference

3 August 2017

14

1 reference

inferred from page(s)

published in

EMBO Molecular Medicine

1 reference

3 August 2017

2

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3 August 2017

12

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3 August 2017

490-503

1 reference

describes a project that uses

3 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3044888/fullTextXML

inferred from PubMed Central ID database lookup

cites work

Cargo recognition failure is responsible for inefficient autophagy in Huntington's disease

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Serines 13 and 16 are critical determinants of full-length human mutant huntingtin induced disease pathogenesis in HD mice

7 July 2018

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Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function

7 July 2018

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IKK phosphorylates Huntingtin and targets it for degradation by the proteasome and lysosome.

7 July 2018

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Coassembly of Mgm1 isoforms requires cardiolipin and mediates mitochondrial inner membrane fusion

7 July 2018

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Mitochondria in Huntington's disease

7 July 2018

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Mitochondrial dynamics in mammalian health and disease

7 July 2018

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Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice

7 July 2018

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Loss of parkin or PINK1 function increases Drp1-dependent mitochondrial fragmentation

7 July 2018

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Complex II inhibition by 3-NP causes mitochondrial fragmentation and neuronal cell death via an NMDA- and ROS-dependent pathway.

7 July 2018

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Regulator of calcineurin (RCAN1-1L) is deficient in Huntington disease and protective against mutant huntingtin toxicity in vitro

7 July 2018

1 reference

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Mitofusin 2 tethers endoplasmic reticulum to mitochondria

7 July 2018

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Effects of overexpression of huntingtin proteins on mitochondrial integrity

7 July 2018

1 reference

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Dephosphorylation by calcineurin regulates translocation of Drp1 to mitochondria

7 July 2018

1 reference

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Opa1-mediated cristae opening is Bax/Bak and BH3 dependent, required for apoptosis, and independent of Bak oligomerization

7 July 2018

1 reference

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N-terminal mutant huntingtin associates with mitochondria and impairs mitochondrial trafficking

7 July 2018

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The PINK1/Parkin pathway regulates mitochondrial morphology

7 July 2018

1 reference

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Calcineurin is involved in the early activation of NMDA-mediated cell death in mutant huntingtin knock-in striatal cells

7 July 2018

1 reference

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Reversible phosphorylation of Drp1 by cyclic AMP-dependent protein kinase and calcineurin regulates mitochondrial fission and cell death

7 July 2018

1 reference

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Mitochondrial dynamics in disease

7 July 2018

1 reference

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Genotype-dependent priming to self- and xeno-cannibalism in heterozygous and homozygous lymphoblasts from patients with Huntington's disease

7 July 2018

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OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion

7 July 2018

1 reference

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Mitochondrial rhomboid PARL regulates cytochrome c release during apoptosis via OPA1-dependent cristae remodeling

7 July 2018

1 reference

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Endoplasmic reticulum BIK initiates DRP1-regulated remodelling of mitochondrial cristae during apoptosis.

7 July 2018

1 reference

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Disturbed Ca2+ signaling and apoptosis of medium spiny neurons in Huntington's disease.

7 July 2018

1 reference

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FK506 prevents mitochondrial-dependent apoptotic cell death induced by 3-nitropropionic acid in rat primary cortical cultures

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

OPA1 requires mitofusin 1 to promote mitochondrial fusion

7 July 2018

1 reference

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Mutant huntingtin directly increases susceptibility of mitochondria to the calcium-induced permeability transition and cytochrome c release

7 July 2018

1 reference

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Cell death: critical control points

7 July 2018

1 reference

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Mitochondrial fission in apoptosis, neurodegeneration and aging

7 July 2018

1 reference

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Transcriptional abnormalities in Huntington disease

7 July 2018

1 reference

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Interactions between ionotropic and metabotropic glutamate receptors regulate cAMP response element-binding protein phosphorylation in cultured striatal neurons

7 July 2018

1 reference

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Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

A distinct pathway remodels mitochondrial cristae and mobilizes cytochrome c during apoptosis

7 July 2018

1 reference

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Huntingtin is present in the nucleus, interacts with the transcriptional corepressor C-terminal binding protein, and represses transcription

7 July 2018

1 reference

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The role of dynamin-related protein 1, a mediator of mitochondrial fission, in apoptosis

7 July 2018

1 reference

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Altered proteasomal function due to the expression of polyglutamine-expanded truncated N-terminal huntingtin induces apoptosis by caspase activation through mitochondrial cytochrome c release

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

tBID, a membrane-targeted death ligand, oligomerizes BAK to release cytochrome c

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

Inhibiting caspase cleavage of huntingtin reduces toxicity and aggregate formation in neuronal and nonneuronal cells

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

Bioenergetics in Huntington's disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

The influence of huntingtin protein size on nuclear localization and cellular toxicity.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

Subcellular localization of the Huntington's disease gene product in cell lines by immunofluorescence and biochemical subcellular fractionation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

Trinucleotide repeat length instability and age of onset in Huntington's disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neurons

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

Widespread expression of Huntington's disease gene (IT15) protein product

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

Expression of the Huntington's disease (IT15) protein product in HD patients

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

Identification and localization of huntingtin in brain and human lymphoblastoid cell lines with anti-fusion protein antibodies

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

Huntington's disease. Pathogenesis and management

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

Proliferative and degenerative changes in striatal spiny neurons in Huntington's disease: a combined study using the section-Golgi method and calbindin D28k immunocytochemistry

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044888

Transcriptional repression of PGC-1alpha by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration.

7 July 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.201000102

Mitochondrial sensitivity and altered calcium handling underlie enhanced NMDA-induced apoptosis in YAC128 model of Huntington's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.201000102

Cleavage at the caspase-6 site is required for neuronal dysfunction and degeneration due to mutant huntingtin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.201000102

Disruption of Axonal Transport by Loss of Huntingtin or Expression of Pathogenic PolyQ Proteins in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.201000102

Calcineurin inhibitors cause an acceleration of the neurological phenotype in a mouse transgenic for the human Huntington's disease mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.201000102

Loss of Drp1 function alters OPA1 processing and changes mitochondrial membrane organization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.201000102

Inhibition of calcineurin by FK506 protects against polyglutamine-huntingtin toxicity through an increase of huntingtin phosphorylation at S421.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.201000102

Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.201000102

Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.201000102

Increased sensitivity to N-methyl-D-aspartate receptor-mediated excitotoxicity in a mouse model of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.201000102

Intra- and intermolecular domain interactions of the C-terminal GTPase effector domain of the multimeric dynamin-like GTPase Drp1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.201000102

Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21069748

12 December 2020

inferred from PubMed ID database lookup

Increased apoptosis of Huntington disease lymphoblasts associated with repeat length-dependent mitochondrial depolarization

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21069748

12 December 2020

inferred from PubMed ID database lookup

The victorin-induced mitochondrial permeability transition precedes cell shrinkage and biochemical markers of cell death, and shrinkage occurs without loss of membrane integrity.

1 reference

https://api.crossref.org/works/10.1002%2FEMMM.201000102

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1002/EMMM.201000102

1 reference

3 August 2017

1 reference

3 August 2017

1 reference