Suppr超能文献

周围神经病中轴索运输障碍:从住院医师杰克的发现到近期的贡献。

Axonal transport disruption in peripheral nerve disease: From Jack's discoveries as a resident to recent contributions.

机构信息

Department of Neurology and Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

J Peripher Nerv Syst. 2012 Dec;17 Suppl 3(0 3):46-51. doi: 10.1111/j.1529-8027.2012.00431.x.

Abstract

Many neurodegenerative diseases and neuropathies have been proposed to be caused by a disruption of axonal transport. However, the mechanisms whereby impaired transport causes disease remain unclear. Proposed mechanisms include impairment in delivery of organelles such as mitochondria, defective retrograde neurotrophic signaling, and disruption of the synaptic vesicle cycle within the synaptic terminal. Simple model organisms such as the fruitfly, Drosophila melanogaster, allow live imaging of axonal transport to be combined with high-throughput genetic screens and are providing insights into the pathophysiology of peripheral nerve diseases.

摘要

许多神经退行性疾病和神经病变被认为是由轴突运输中断引起的。然而,运输受损导致疾病的确切机制尚不清楚。提出的机制包括细胞器(如线粒体)的输送受损、逆行神经营养信号的缺陷,以及突触末梢内突触小泡循环的破坏。简单的模式生物,如黑腹果蝇,允许对轴突运输进行活体成像,同时结合高通量遗传筛选,为周围神经疾病的病理生理学提供了新的见解。

相似文献

1
Axonal transport disruption in peripheral nerve disease: From Jack's discoveries as a resident to recent contributions.
J Peripher Nerv Syst. 2012 Dec;17 Suppl 3(0 3):46-51. doi: 10.1111/j.1529-8027.2012.00431.x.
2
Defective axonal transport: A common pathological mechanism in inherited and acquired peripheral neuropathies.
Neurobiol Dis. 2017 Sep;105:300-320. doi: 10.1016/j.nbd.2017.02.009. Epub 2017 Feb 24.
3
Defects in Axonal Transport in Inherited Neuropathies.
J Neuromuscul Dis. 2019;6(4):401-419. doi: 10.3233/JND-190427.
5
Axonal transport of synaptic vesicle proteins in the rat optic nerve.
J Neurobiol. 1997 Feb;32(2):237-50. doi: 10.1002/(sici)1097-4695(199702)32:2<237::aid-neu8>3.0.co;2-9.
6
Axonal transport, imaging, and the diagnosis of nerve compression.
Br J Neurosurg. 1992;6(4):293-5. doi: 10.3109/02688699209023786.
8
Axonal transport of ribonucleoprotein particles (vaults).
Neuroscience. 1999;91(3):1055-65. doi: 10.1016/s0306-4522(98)00622-8.
10

引用本文的文献

1
Cisplatin induces mitochondrial deficits in Drosophila larval segmental nerve.
Neurobiol Dis. 2017 Jan;97(Pt A):60-69. doi: 10.1016/j.nbd.2016.10.003. Epub 2016 Oct 17.
2
Drosophila Neuronal Injury Follows a Temporal Sequence of Cellular Events Leading to Degeneration at the Neuromuscular Junction.
J Exp Neurosci. 2015 Oct 18;9(Suppl 2):1-9. doi: 10.4137/JEN.S25516. eCollection 2015.

本文引用的文献

1
The p150(Glued) CAP-Gly domain regulates initiation of retrograde transport at synaptic termini.
Neuron. 2012 Apr 26;74(2):344-60. doi: 10.1016/j.neuron.2012.02.026.
2
The CAP-Gly of p150: one domain, two diseases, and a function at the end.
Neuron. 2012 Apr 26;74(2):211-3. doi: 10.1016/j.neuron.2012.04.003.
3
Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy.
Neurology. 2012 May 29;78(22):1714-20. doi: 10.1212/WNL.0b013e3182556c05. Epub 2012 Mar 28.
4
Neuropeptide delivery to synapses by long-range vesicle circulation and sporadic capture.
Cell. 2012 Mar 2;148(5):1029-38. doi: 10.1016/j.cell.2011.12.036.
5
Exome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth disease.
Am J Hum Genet. 2011 Aug 12;89(2):308-12. doi: 10.1016/j.ajhg.2011.07.002. Epub 2011 Aug 4.
6
KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2.
Am J Hum Genet. 2011 Aug 12;89(2):219-30. doi: 10.1016/j.ajhg.2011.06.013. Epub 2011 Aug 4.
7
Neuronal intracellular transport and neurodegenerative disease.
Neurology. 2011 Mar 15;76(11):1015-20. doi: 10.1212/WNL.0b013e31821103f7.
8
Flightless flies: Drosophila models of neuromuscular disease.
Ann N Y Acad Sci. 2010 Jan;1184:e1-20. doi: 10.1111/j.1749-6632.2010.05432.x.
9
Compartmentalized microfluidic culture platform to study mechanism of paclitaxel-induced axonal degeneration.
Exp Neurol. 2009 Jul;218(1):124-8. doi: 10.1016/j.expneurol.2009.04.017. Epub 2009 May 3.
10
DCTN1 mutations in Perry syndrome.
Nat Genet. 2009 Feb;41(2):163-5. doi: 10.1038/ng.293. Epub 2009 Jan 11.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验