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本文引用的文献

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Axon regeneration genes identified by RNAi screening in C. elegans.通过 RNAi 筛选在秀丽隐杆线虫中鉴定的轴突再生基因。
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2
Nerve injury induces the expression of syndecan-1 heparan sulfate proteoglycan in peripheral motor neurons.神经损伤诱导周围运动神经元中 syndecan-1 硫酸乙酰肝素蛋白聚糖的表达。
Neurosci Lett. 2012 Oct 3;527(1):28-33. doi: 10.1016/j.neulet.2012.08.043. Epub 2012 Sep 1.
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Direct visualization of specifically modified extracellular glycans in living animals.在活体动物中直接可视化特异性修饰的细胞外糖链。
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Growth cone travel in space and time: the cellular ensemble of cytoskeleton, adhesion, and membrane.生长锥在空间和时间中的运动:细胞骨架、黏附与膜的整体组合。
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Assembly of a new growth cone after axotomy: the precursor to axon regeneration.轴突切断后新生长锥的组装:轴突再生的前体。
Nat Rev Neurosci. 2012 Feb 15;13(3):183-93. doi: 10.1038/nrn3176.
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Improved Mos1-mediated transgenesis in C. elegans.秀丽隐杆线虫中经改进的Mos1介导的转基因技术。
Nat Methods. 2012 Jan 30;9(2):117-8. doi: 10.1038/nmeth.1865.
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Notch signaling inhibits axon regeneration.Notch 信号抑制轴突再生。
Neuron. 2012 Jan 26;73(2):268-78. doi: 10.1016/j.neuron.2011.11.017.
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Laser microsurgery in Caenorhabditis elegans.秀丽隐杆线虫中的激光显微手术。
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9
A syndecan-4 hair trigger initiates wound healing through caveolin- and RhoG-regulated integrin endocytosis.硫酸乙酰肝素蛋白聚糖-4 作为“发夹触发器”,通过小窝蛋白和 RhoG 调节的整合素内吞作用启动伤口愈合。
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10
Axon regeneration pathways identified by systematic genetic screening in C. elegans.通过在秀丽隐杆线虫中的系统遗传筛选鉴定出的轴突再生途径。
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Syndecan通过稳定生长锥迁移来促进轴突再生。

Syndecan promotes axon regeneration by stabilizing growth cone migration.

作者信息

Edwards Tyson J, Hammarlund Marc

机构信息

Department of Genetics, Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, BCMM 436E, 295 Congress Avenue, New Haven, CT 06510, USA.

Department of Genetics, Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, BCMM 436E, 295 Congress Avenue, New Haven, CT 06510, USA.

出版信息

Cell Rep. 2014 Jul 10;8(1):272-83. doi: 10.1016/j.celrep.2014.06.008. Epub 2014 Jul 4.

DOI:10.1016/j.celrep.2014.06.008
PMID:25001284
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4127196/
Abstract

Growth cones facilitate the repair of nervous system damage by providing the driving force for axon regeneration. Using single-neuron laser axotomy and in vivo time-lapse imaging, we show that syndecan, a heparan sulfate (HS) proteoglycan, is required for growth cone function during axon regeneration in C. elegans. In the absence of syndecan, regenerating growth cones form but are unstable and collapse, decreasing the effective growth rate and impeding regrowth to target cells. We provide evidence that syndecan has two distinct functions during axon regeneration: (1) a canonical function in axon guidance that requires expression outside the nervous system and depends on HS chains and (2) an intrinsic function in growth cone stabilization that is mediated by the syndecan core protein, independently of HS. Thus, syndecan is a regulator of a critical choke point in nervous system repair.

摘要

生长锥通过为轴突再生提供驱动力来促进神经系统损伤的修复。利用单神经元激光轴突切断术和体内延时成像技术,我们发现,在秀丽隐杆线虫轴突再生过程中,硫酸乙酰肝素蛋白聚糖syndecan是生长锥功能所必需的。在缺乏syndecan的情况下,再生生长锥虽能形成,但不稳定且会塌陷,从而降低有效生长速率并阻碍向靶细胞的再生长。我们提供的证据表明,syndecan在轴突再生过程中具有两种不同的功能:(1)在轴突导向中的经典功能,这需要在神经系统外表达且依赖于硫酸乙酰肝素链;(2)在生长锥稳定中的内在功能,这由syndecan核心蛋白介导,独立于硫酸乙酰肝素。因此,syndecan是神经系统修复中一个关键瓶颈点的调节因子。