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Axotomized rubrospinal neurons rescued by fetal spinal cord transplants maintain axon collaterals to rostral CNS targets.经胎儿脊髓移植挽救的轴突切断的红核脊髓神经元维持着向脑前部中枢神经系统靶标的轴突侧支。
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Brain-derived neurotrophic factor gene transfer with adeno-associated viral and lentiviral vectors prevents rubrospinal neuronal atrophy and stimulates regeneration-associated gene expression after acute cervical spinal cord injury.腺相关病毒和慢病毒载体介导的脑源性神经营养因子基因转移可预防急性颈脊髓损伤后红核脊髓束神经元萎缩并刺激再生相关基因表达。
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Use of self-complementary adeno-associated virus serotype 2 as a tracer for labeling axons: implications for axon regeneration.使用自我互补腺相关病毒2型作为标记轴突的示踪剂:对轴突再生的影响。
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本文引用的文献

1
Targeting a dominant negative rho kinase to neurons promotes axonal outgrowth and partial functional recovery after rat rubrospinal tract lesion.靶向神经元中的显性负性 Rho 激酶可促进大鼠红核脊髓束损伤后的轴突生长和部分功能恢复。
Mol Ther. 2009 Dec;17(12):2020-30. doi: 10.1038/mt.2009.168. Epub 2009 Jul 21.
2
CAR-associated vesicular transport of an adenovirus in motor neuron axons.腺病毒在运动神经元轴突中与CAR相关的囊泡运输。
PLoS Pathog. 2009 May;5(5):e1000442. doi: 10.1371/journal.ppat.1000442. Epub 2009 May 22.
3
Chronic spinal hemisection in rats induces a progressive decline in transmission in uninjured fibers to motoneurons.大鼠慢性脊髓半切术会导致未受损纤维向运动神经元的传递逐渐下降。
Exp Neurol. 2009 Apr;216(2):471-80. doi: 10.1016/j.expneurol.2009.01.004.
4
Retrograde adenoviral vector targeting of nociresponsive pontospinal noradrenergic neurons in the rat in vivo.体内大鼠伤害性反应性脑桥脊髓去甲肾上腺素能神经元的逆行腺病毒载体靶向
J Comp Neurol. 2009 Jan 10;512(2):141-57. doi: 10.1002/cne.21879.
5
Repulsive Wnt signaling inhibits axon regeneration after CNS injury.排斥性Wnt信号传导抑制中枢神经系统损伤后的轴突再生。
J Neurosci. 2008 Aug 13;28(33):8376-82. doi: 10.1523/JNEUROSCI.1939-08.2008.
6
Adenovirus-mediated retrograde transfer of neurotrophin-3 gene enhances survival of anterior horn neurons of twy/twy mice with chronic mechanical compression of the spinal cord.腺病毒介导的神经营养因子-3基因逆行转移可提高脊髓慢性机械压迫的twy/twy小鼠前角神经元的存活率。
J Neurosci Res. 2008 Jun;86(8):1789-800. doi: 10.1002/jnr.21627.
7
Targeting axon growth from neuronal transplants along preformed guidance pathways in the adult CNS.靶向成年中枢神经系统中沿预先形成的引导通路的神经元移植的轴突生长。
J Neurosci. 2008 Jan 9;28(2):340-8. doi: 10.1523/JNEUROSCI.3819-07.2008.
8
Behavioral, histological, and ex vivo magnetic resonance imaging assessment of graded contusion spinal cord injury in mice.小鼠分级挫伤性脊髓损伤的行为学、组织学及体外磁共振成像评估
J Neurotrauma. 2007 Apr;24(4):674-89. doi: 10.1089/neu.2006.0204.
9
Interaction of adenovirus type 5 fiber with the coxsackievirus and adenovirus receptor activates inflammatory response in human respiratory cells.5型腺病毒纤维与柯萨奇病毒和腺病毒受体的相互作用激活人呼吸道细胞中的炎症反应。
J Virol. 2006 Nov;80(22):11241-54. doi: 10.1128/JVI.00721-06. Epub 2006 Sep 6.
10
Gene delivery to the spinal cord: comparison between lentiviral, adenoviral, and retroviral vector delivery systems.基因传递至脊髓:慢病毒、腺病毒和逆转录病毒载体传递系统的比较
J Neurosci Res. 2006 Aug 15;84(3):553-67. doi: 10.1002/jnr.20968.

腺病毒-GFP 对红核脊髓束的优先和双向标记,用于监测正常和损伤的轴突。

Preferential and bidirectional labeling of the rubrospinal tract with adenovirus-GFP for monitoring normal and injured axons.

机构信息

Spinal Cord and Brain Injury Research Group, Stark Neurosciences Research Institute, and Department of Neurological Surgery, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.

出版信息

J Neurotrauma. 2011 Apr;28(4):635-47. doi: 10.1089/neu.2010.1566. Epub 2011 Mar 24.

DOI:10.1089/neu.2010.1566
PMID:21299337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3070148/
Abstract

The rodent rubrospinal tract (RST) has been studied extensively to investigate regeneration and remodeling of central nervous system (CNS) axons. Currently no retrograde tracers can specifically label rubrospinal axons and neurons (RSNs). The RST can be anterogradely labeled by injecting tracers into the red nucleus (RN), but accurately locating the RN is a technical challenge. Here we developed a recombinant adenovirus carrying a green fluorescent protein reporter gene (Adv-GFP) which can preferentially, intensely, and bi-directionally label the RST. When Adv-GFP was injected into the second lumbar spinal cord, the GFP was specifically transported throughout the entire RST, with peak labeling seen at 2 weeks post-injection. When Adv-GFP was injected directly into the RN, GFP was anterogradely transported throughout the RST. Following spinal cord injury (SCI), injection of Adv-GFP resulted in visualization of GFP in transected, spared, or sprouted RST axons bi-directionally. Thus Adv-GFP could be used as a novel tool for monitoring and evaluating strategies designed to maximize RST axonal regeneration and remodeling following SCI.

摘要

啮齿动物红核脊髓束(RST)已被广泛研究,以研究中枢神经系统(CNS)轴突的再生和重塑。目前没有逆行示踪剂可以特异性标记红核脊髓束轴突和神经元(RSNs)。可以通过将示踪剂注射到红核(RN)中来顺行标记 RST,但准确定位 RN 是一个技术挑战。在这里,我们开发了一种携带绿色荧光蛋白报告基因(Adv-GFP)的重组腺病毒,该病毒可以优先、强烈和双向标记 RST。当 Adv-GFP 注射到第二腰椎脊髓时,GFP 特异性地运输到整个 RST,在注射后 2 周时达到峰值标记。当 Adv-GFP 直接注射到 RN 时,GFP 被顺行运输到整个 RST。在脊髓损伤(SCI)后,Adv-GFP 的注射导致 GFP 在横断、保留或发芽的 RST 轴突中双向可视化。因此,Adv-GFP 可作为一种新工具,用于监测和评估旨在最大限度地促进 SCI 后 RST 轴突再生和重塑的策略。