Reversible disruption of dynactin 1-mediated retrograde axonal transport in polyglutamine-induced motor neuron degeneration. (Q52575167)

PubMed publication ID

17122035

3 May 2018

http://europepmc.org/abstract/MED/17122035

title

Reversible disruption of dynactin 1-mediated retrograde axonal transport in polyglutamine-induced motor neuron degeneration (English)

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11 May 2020

2

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11 May 2020

author name string

Masahisa Katsuno

1

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11 May 2020

Makoto Minamiyama

3

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11 May 2020

Masahiro Waza

4

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11 May 2020

Keisuke Tokui

5

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11 May 2020

Haruhiko Banno

6

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11 May 2020

Keisuke Suzuki

7

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11 May 2020

Yu Onoda

8

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11 May 2020

Fumiaki Tanaka

9

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11 May 2020

Manabu Doyu

10

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11 May 2020

Gen Sobue

11

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11 May 2020

language of work or name

English

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publication date

1 November 2006

1 reference

PubMed publication ID

17122035

3 May 2018

http://europepmc.org/abstract/MED/17122035

published in

Journal of Neuroscience

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11 May 2020

volume

26

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11 May 2020

issue

47

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11 May 2020

page(s)

12106-12117

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Chaperones Hsp70 and Hsp40 suppress aggregate formation and apoptosis in cultured neuronal cells expressing truncated androgen receptor protein with expanded polyglutamine tract

11 May 2020

cites work

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Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease

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Cytoplasmic dynein conversion at a crush injury in rat peripheral axons

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Transcriptional dysregulation in Huntington's disease

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CREB-binding protein sequestration by expanded polyglutamine

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Neurofilaments are transported rapidly but intermittently in axons: implications for slow axonal transport.

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Interference by huntingtin and atrophin-1 with cbp-mediated transcription leading to cellular toxicity

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Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila

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Neurofilament accumulation at the motor endplate and lack of axonal sprouting in a spinal muscular atrophy mouse model

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Disruption of dynein/dynactin inhibits axonal transport in motor neurons causing late-onset progressive degeneration.

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X-Linked inhibitor of apoptosis protein is involved in mutant SOD1-mediated neuronal degeneration

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Androgen receptor with elongated polyglutamine tract forms aggregates that alter axonal trafficking and mitochondrial distribution in motor neuronal processes

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Expression of X-linked bulbospinal muscular atrophy (Kennedy disease) in two homozygous women

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Testosterone reduction prevents phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy

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Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor, ameliorates motor deficits in a mouse model of Huntington's disease

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Mutant dynactin in motor neuron disease.

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Heat shock protein 70 chaperone overexpression ameliorates phenotypes of the spinal and bulbar muscular atrophy transgenic mouse model by reducing nuclear-localized mutant androgen receptor protein

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Transcriptional abnormalities in Huntington disease

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Caspase-1 and -3 mRNAs are differentially upregulated in motor neurons and glial cells in mutant SOD1 transgenic mouse spinal cord: a study using laser microdissection and real-time RT-PCR.

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Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy

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

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Neuropathogenic forms of huntingtin and androgen receptor inhibit fast axonal transport

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Androgen receptor YAC transgenic mice recapitulate SBMA motor neuronopathy and implicate VEGF164 in the motor neuron degeneration

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Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy

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12 December 2020

Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease

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Castration restores function and neurofilament alterations of aged symptomatic males in a transgenic mouse model of spinal and bulbar muscular atrophy.

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Recovery from polyglutamine-induced neurodegeneration in conditional SCA1 transgenic mice.

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Progressive abnormalities in skeletal muscle and neuromuscular junctions of transgenic mice expressing the Huntington's disease mutation

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Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients.

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Gene expression profile of spinal motor neurons in sporadic amyotrophic lateral sclerosis

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Role of cytoplasmic dynein in the axonal transport of microtubules and neurofilaments

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Distal spinal and bulbar muscular atrophy caused by dynactin mutation.

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12 December 2020

17-AAG, an Hsp90 inhibitor, ameliorates polyglutamine-mediated motor neuron degeneration

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Diseases of unstable repeat expansion: mechanisms and common principles

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Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD.

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Pharmacological induction of heat-shock proteins alleviates polyglutamine-mediated motor neuron disease

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Mutant androgen receptor accumulation in spinal and bulbar muscular atrophy scrotal skin: a pathogenic marker

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Efficient selection for high-expression transfectants with a novel eukaryotic vector

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JNK mediates pathogenic effects of polyglutamine-expanded androgen receptor on fast axonal transport

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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

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12 December 2020

Phosphorylated high molecular weight neurofilament protein in lower motor neurons in amyotrophic lateral sclerosis and other neurodegenerative diseases involving ventral horn cells

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X-linked recessive bulbospinal neuronopathy. A clinicopathological study

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Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait

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Benzodiazepine and GABA receptors in early Huntington's disease

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Androgen receptor mRNA with increased size of tandem CAG repeat is widely expressed in the neural and nonneural tissues of X-linked recessive bulbospinal neuronopathy

1 reference

12 December 2020

Rab3a, a small GTP-binding protein, undergoes fast anterograde transport but not retrograde transport in neurons

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12 December 2020

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

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12 December 2020

Purkinje cell expression of a mutant allele of SCA1 in transgenic mice leads to disparate effects on motor behaviors, followed by a progressive cerebellar dysfunction and histological alterations.

1 reference

12 December 2020

Differential effects of neurotrophic factors on motoneuron retrograde labeling in a murine model of motoneuron disease.

1 reference

12 December 2020

10.1523/JNEUROSCI.3032-06.2006

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6675422&resulttype=core&format=json

11 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6675422&resulttype=core&format=json

11 May 2020

PubMed publication ID

17122035

1 reference