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本文引用的文献

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Direct Lineage Reprogramming Reveals Disease-Specific Phenotypes of Motor Neurons from Human ALS Patients.直接谱系重编程揭示了人类肌萎缩侧索硬化症(ALS)患者运动神经元的疾病特异性表型。
Cell Rep. 2016 Jan 5;14(1):115-128. doi: 10.1016/j.celrep.2015.12.018. Epub 2015 Dec 24.
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Modeling amyotrophic lateral sclerosis in pure human iPSc-derived motor neurons isolated by a novel FACS double selection technique.通过新型 FACS 双选技术分离的纯人 iPSC 衍生运动神经元中肌萎缩侧索硬化症的建模。
Neurobiol Dis. 2015 Oct;82:269-280. doi: 10.1016/j.nbd.2015.06.011. Epub 2015 Jun 21.
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209th ENMC International Workshop: Outcome Measures and Clinical Trial Readiness in Spinal Muscular Atrophy 7-9 November 2014, Heemskerk, The Netherlands.第209届ENMC国际研讨会:脊髓性肌萎缩症的疗效指标与临床试验准备情况,2014年11月7日至9日,荷兰赫姆斯凯尔克
Neuromuscul Disord. 2015 Jul;25(7):593-602. doi: 10.1016/j.nmd.2015.04.009. Epub 2015 Apr 28.
4
Peripheral injury of pelvic visceral sensory nerves alters GFRα (GDNF family receptor alpha) localization in sensory and autonomic pathways of the sacral spinal cord.盆腔内脏感觉神经的外周损伤会改变骶脊髓感觉和自主神经通路中GFRα(胶质细胞源性神经营养因子家族受体α)的定位。
Front Neuroanat. 2015 Apr 10;9:43. doi: 10.3389/fnana.2015.00043. eCollection 2015.
5
Motor neurons with differential vulnerability to degeneration show distinct protein signatures in health and ALS.对变性具有不同易损性的运动神经元在健康状态和肌萎缩侧索硬化症中表现出不同的蛋白质特征。
Neuroscience. 2015 Apr 16;291:216-29. doi: 10.1016/j.neuroscience.2015.02.013. Epub 2015 Feb 16.
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The phenotypic variability of amyotrophic lateral sclerosis.肌萎缩侧索硬化症的表型变异性。
Nat Rev Neurol. 2014 Nov;10(11):661-70. doi: 10.1038/nrneurol.2014.184. Epub 2014 Oct 14.
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Evolving Hox activity profiles govern diversity in locomotor systems.Hox 基因活性谱的演变控制着运动系统的多样性。
Dev Cell. 2014 Apr 28;29(2):171-87. doi: 10.1016/j.devcel.2014.03.008. Epub 2014 Apr 17.
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A phase II-III trial of olesoxime in subjects with amyotrophic lateral sclerosis.奥昔莫司汀治疗肌萎缩侧索硬化症的 II-III 期临床试验。
Eur J Neurol. 2014 Mar;21(3):529-36. doi: 10.1111/ene.12344. Epub 2014 Jan 21.
9
A small molecule screen in stem-cell-derived motor neurons identifies a kinase inhibitor as a candidate therapeutic for ALS.在干细胞衍生的运动神经元中进行的小分子筛选确定了一种激酶抑制剂作为 ALS 的候选治疗药物。
Cell Stem Cell. 2013 Jun 6;12(6):713-26. doi: 10.1016/j.stem.2013.04.003. Epub 2013 Apr 18.
10
EMD 1214063 and EMD 1204831 constitute a new class of potent and highly selective c-Met inhibitors.EMD 1214063 和 EMD 1204831 构成了一类新型强效且高选择性的 c-Met 抑制剂。
Clin Cancer Res. 2013 Jun 1;19(11):2941-51. doi: 10.1158/1078-0432.CCR-12-3247. Epub 2013 Apr 3.

新型组合筛选方法鉴定了选择性运动神经元的神经营养因子。

Novel combinatorial screening identifies neurotrophic factors for selective classes of motor neurons.

机构信息

Institut de Neurosciences de la Timone, UMR 7289 CNRS, Aix-Marseille University, 13005 Marseille, France.

Centre d'Immunologie de Marseille-Luminy (CIML), CNRS, INSERM, Aix-Marseille University, 13288 Marseille, France.

出版信息

Proc Natl Acad Sci U S A. 2017 Mar 21;114(12):E2486-E2493. doi: 10.1073/pnas.1615372114. Epub 2017 Mar 7.

DOI:10.1073/pnas.1615372114
PMID:28270618
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5373341/
Abstract

Numerous neurotrophic factors promote the survival of developing motor neurons but their combinatorial actions remain poorly understood; to address this, we here screened 66 combinations of 12 neurotrophic factors on pure, highly viable, and standardized embryonic mouse motor neurons isolated by a unique FACS technique. We demonstrate potent, strictly additive, survival effects of hepatocyte growth factor (HGF), ciliary neurotrophic factor (CNTF), and Artemin through specific activation of their receptor complexes in distinct subsets of lumbar motor neurons: HGF supports hindlimb motor neurons through c-Met; CNTF supports subsets of axial motor neurons through CNTFRα; and Artemin acts as the first survival factor for parasympathetic preganglionic motor neurons through GFRα3/Syndecan-3 activation. These data show that neurotrophic factors can selectively promote the survival of distinct classes of embryonic motor neurons. Similar studies on postnatal motor neurons may provide a conceptual framework for the combined therapeutic use of neurotrophic factors in degenerative motor neuron diseases such as amyotrophic lateral sclerosis, spinal muscular atrophy, and spinobulbar muscular atrophy.

摘要

许多神经营养因子促进运动神经元的存活,但它们的组合作用仍知之甚少;为了解决这个问题,我们在这里筛选了 12 种神经营养因子的 66 种组合,这些因子是通过独特的 FACS 技术从纯、高活力和标准化的胚胎小鼠运动神经元中分离出来的。我们通过特定的受体复合物激活,证明了肝细胞生长因子(HGF)、睫状神经营养因子(CNTF)和 Artemin 的强大、严格的、附加的生存效应,这些因子在不同的腰运动神经元亚群中发挥作用:HGF 通过 c-Met 支持后肢运动神经元;CNTF 通过 CNTFRα 支持轴突运动神经元的亚群;Artemin 通过 GFRα3/Syndecan-3 的激活作为副交感节前运动神经元的第一个存活因子。这些数据表明,神经营养因子可以选择性地促进不同类型的胚胎运动神经元的存活。对出生后运动神经元的类似研究可能为联合使用神经营养因子治疗肌萎缩侧索硬化症、脊髓性肌萎缩症和延髓性肌萎缩症等退行性运动神经元疾病提供一个概念框架。