Calcium homeostasis and mitochondrial dysfunction in striatal neurons of Huntington disease (Q40031554)

16 September 2017

title

Calcium homeostasis and mitochondrial dysfunction in striatal neurons of Huntington disease (English)

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16 September 2017

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16 September 2017

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16 September 2017

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16 September 2017

Chiara Zuccato

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Dmitry Lim

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object named as

Dmitry Lim

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16 September 2017

Laura Fedrizzi

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16 September 2017

Marzia Tartari

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16 September 2017

language of work or name

English

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publication date

21 December 2007

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Journal of Biological Chemistry

16 September 2017

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inferred from page(s)

published in

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16 September 2017

volume

283

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16 September 2017

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16 September 2017

page(s)

5780-5789

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

16 September 2017

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Mitochondrial respiration and ATP production are significantly impaired in striatal cells expressing mutant huntingtin

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HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism

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PGC-1alpha deficiency causes multi-system energy metabolic derangements: muscle dysfunction, abnormal weight control and hepatic steatosis

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

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Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1alpha in Huntington's disease neurodegeneration

21 January 2018

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

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Role of brain-derived neurotrophic factor in Huntington's disease

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Huntingtin and huntingtin-associated protein 1 influence neuronal calcium signaling mediated by inositol-(1,4,5) triphosphate receptor type 1

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Decreased expression of striatal signaling genes in a mouse model of Huntington's disease

21 January 2018

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Mutant huntingtin's effects on striatal gene expression in mice recapitulate changes observed in human Huntington's disease brain and do not differ with mutant huntingtin length or wild-type huntingtin dosage

21 January 2018

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Mutant huntingtin expression induces mitochondrial calcium handling defects in clonal striatal cells: functional consequences

21 January 2018

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

21 January 2018

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Increased formation of reactive oxygen species, but no changes in glutathione peroxidase activity, in striata of mice transgenic for the Huntington's disease mutation

21 January 2018

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21 January 2018

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Striatal neuronal apoptosis is preferentially enhanced by NMDA receptor activation in YAC transgenic mouse model of Huntington disease

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Cell death triggered by polyglutamine-expanded huntingtin in a neuronal cell line is associated with degradation of CREB-binding protein

21 January 2018

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In vitro analysis of huntingtin-mediated transcriptional repression reveals multiple transcription factor targets

21 January 2018

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Preferential mitochondrial DNA injury caused by glucose oxidase as a steady generator of hydrogen peroxide in human fibroblasts

21 January 2018

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Cell sorting experiments link persistent mitochondrial DNA damage with loss of mitochondrial membrane potential and apoptotic cell death

21 January 2018

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Mitochondrial DNA damage is more extensive and persists longer than nuclear DNA damage in human cells following oxidative stress

21 January 2018

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Involvement of mitochondrial complex II defects in neuronal death produced by N-terminus fragment of mutated huntingtin

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1,2,3,4-Tetrahydroisoquinoline protects terminals of dopaminergic neurons in the striatum against the malonate-induced neurotoxicity

21 January 2018

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21 January 2018

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Parenterally administered 3-nitropropionic acid and amphetamine can combine to produce damage to terminals and cell bodies in the striatum

21 January 2018

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Calcium-dependent cleavage of endogenous wild-type huntingtin in primary cortical neurons

21 January 2018

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21 January 2018

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

21 January 2018

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HAP1 facilitates effects of mutant huntingtin on inositol 1,4,5-trisphosphate-induced Ca release in primary culture of striatal medium spiny neurons

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M704704200

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16 September 2017

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