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Gene delivery to overcome astrocyte inhibition of axonal growth: an in vitro model of the glial scar.基因传递以克服星形胶质细胞对轴突生长的抑制:神经胶质瘢痕的体外模型。
Biotechnol Bioeng. 2013 Mar;110(3):947-57. doi: 10.1002/bit.24750. Epub 2012 Nov 1.
2
ROCK inhibition with Y27632 activates astrocytes and increases their expression of neurite growth-inhibitory chondroitin sulfate proteoglycans.用Y27632抑制ROCK可激活星形胶质细胞并增加其神经突生长抑制性硫酸软骨素蛋白聚糖的表达。
Glia. 2007 Mar;55(4):369-84. doi: 10.1002/glia.20466.
3
Overcoming neurite-inhibitory chondroitin sulfate proteoglycans in the astrocyte matrix.克服星形胶质细胞基质中的神经突抑制性硫酸软骨素蛋白聚糖。
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4
Molecular mechanisms of scar-sourced axon growth inhibitors.瘢痕源性轴突生长抑制剂的分子机制。
Brain Res. 2015 Sep 4;1619:22-35. doi: 10.1016/j.brainres.2014.08.064. Epub 2014 Sep 1.
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Chondroitin sulfate proteoglycans inhibit oligodendrocyte myelination through PTPσ.硫酸软骨素蛋白聚糖通过 PTPσ 抑制少突胶质细胞髓鞘形成。
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Inhibiting glycosaminoglycan chain polymerization decreases the inhibitory activity of astrocyte-derived chondroitin sulfate proteoglycans.抑制糖胺聚糖链聚合会降低星形胶质细胞衍生的硫酸软骨素蛋白聚糖的抑制活性。
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Lentiviral vector-mediated knockdown of the NG2 [corrected] proteoglycan or expression of neurotrophin-3 promotes neurite outgrowth in a cell culture model of the glial scar.慢病毒载体介导的 NG2 [更正] 蛋白聚糖敲低或神经营养因子-3 的表达促进神经突在神经胶质瘢痕细胞培养模型中的生长。
J Gene Med. 2010 Nov;12(11):863-72. doi: 10.1002/jgm.1509. Epub 2010 Oct 26.
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Immature astrocytes promote CNS axonal regeneration when combined with chondroitinase ABC.未成熟的星形胶质细胞与软骨素酶 ABC 联合使用时可促进中枢神经系统轴突再生。
Dev Neurobiol. 2010 Oct;70(12):826-41. doi: 10.1002/dneu.20820.
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Nervous system-derived chondroitin sulfate proteoglycans regulate growth cone morphology and inhibit neurite outgrowth: a light, epifluorescence, and electron microscopy study.神经系统衍生的硫酸软骨素蛋白聚糖调节生长锥形态并抑制神经突生长:一项光学、落射荧光和电子显微镜研究。
Microsc Res Tech. 2001 Sep 1;54(5):273-86. doi: 10.1002/jemt.1140.
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Scar-mediated inhibition and CSPG receptors in the CNS.瘢痕介导的抑制作用和中枢神经系统中的 CSPG 受体。
Exp Neurol. 2012 Oct;237(2):370-8. doi: 10.1016/j.expneurol.2012.07.009. Epub 2012 Jul 24.

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Astrocytes, therapeutic targets for neuroprotection and neurorestoration in ischemic stroke.星形胶质细胞,缺血性脑卒中神经保护和神经修复的治疗靶点。
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本文引用的文献

1
6-Sulphated chondroitins have a positive influence on axonal regeneration.6-硫酸软骨素对轴突再生有积极影响。
PLoS One. 2011;6(7):e21499. doi: 10.1371/journal.pone.0021499. Epub 2011 Jul 1.
2
Chondroitinase combined with rehabilitation promotes recovery of forelimb function in rats with chronic spinal cord injury.软骨素酶联合康复治疗促进慢性脊髓损伤大鼠前肢功能恢复。
J Neurosci. 2011 Jun 22;31(25):9332-44. doi: 10.1523/JNEUROSCI.0983-11.2011.
3
A versatile 3D culture model facilitates monitoring of astrocytes undergoing reactive gliosis.一种多功能的 3D 培养模型有助于监测发生反应性神经胶质增生的星形胶质细胞。
J Tissue Eng Regen Med. 2009 Dec;3(8):634-46. doi: 10.1002/term.209.
4
Chondroitinase ABC treatment opens a window of opportunity for task-specific rehabilitation.软骨素酶ABC治疗为特定任务康复开启了一扇机会之窗。
Nat Neurosci. 2009 Sep;12(9):1145-51. doi: 10.1038/nn.2377. Epub 2009 Aug 9.
5
The bright side of the glial scar in CNS repair.中枢神经系统修复中胶质瘢痕的积极作用。
Nat Rev Neurosci. 2009 Mar;10(3):235-41. doi: 10.1038/nrn2591.
6
Identification of chondroitin sulfate glucuronyltransferase as chondroitin synthase-3 involved in chondroitin polymerization: chondroitin polymerization is achieved by multiple enzyme complexes consisting of chondroitin synthase family members.鉴定硫酸软骨素葡糖醛酸基转移酶为参与硫酸软骨素聚合的软骨素合酶-3:硫酸软骨素聚合是由软骨素合酶家族成员组成的多种酶复合物实现的。
J Biol Chem. 2008 Apr 25;283(17):11396-406. doi: 10.1074/jbc.M707549200. Epub 2008 Mar 3.
7
Inhibiting glycosaminoglycan chain polymerization decreases the inhibitory activity of astrocyte-derived chondroitin sulfate proteoglycans.抑制糖胺聚糖链聚合会降低星形胶质细胞衍生的硫酸软骨素蛋白聚糖的抑制活性。
J Neurosci. 2007 Dec 26;27(52):14494-501. doi: 10.1523/JNEUROSCI.2807-07.2007.
8
Therapeutic time window for the application of chondroitinase ABC after spinal cord injury.脊髓损伤后应用软骨素酶ABC的治疗时间窗。
Exp Neurol. 2008 Apr;210(2):331-8. doi: 10.1016/j.expneurol.2007.11.002. Epub 2007 Nov 21.
9
Effect of body temperature on chondroitinase ABC's ability to cleave chondroitin sulfate glycosaminoglycans.体温对软骨素酶ABC切割硫酸软骨素糖胺聚糖能力的影响。
J Neurosci Res. 2007 Apr;85(5):1110-8. doi: 10.1002/jnr.21199.
10
Involvement of chondroitin sulfate synthase-3 (chondroitin synthase-2) in chondroitin polymerization through its interaction with chondroitin synthase-1 or chondroitin-polymerizing factor.硫酸软骨素合酶-3(软骨素合酶-2)通过与软骨素合酶-1或软骨素聚合因子相互作用参与软骨素聚合。
Biochem J. 2007 May 1;403(3):545-52. doi: 10.1042/BJ20061876.

基因传递以克服星形胶质细胞对轴突生长的抑制:神经胶质瘢痕的体外模型。

Gene delivery to overcome astrocyte inhibition of axonal growth: an in vitro model of the glial scar.

机构信息

Department of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois 60208, USA.

出版信息

Biotechnol Bioeng. 2013 Mar;110(3):947-57. doi: 10.1002/bit.24750. Epub 2012 Nov 1.

DOI:10.1002/bit.24750
PMID:23055330
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4035246/
Abstract

After injury to the central nervous system, a glial scar develops that physically and biochemically inhibits axon growth. In the scar, activated astrocytes secrete inhibitory extracellular matrix, of which chondroitin sulfate proteoglycans (CSPGs) are considered the major inhibitory component. An inhibitory interface of CSPGs forms around the lesion and prevents axons from traversing the injury, and decreasing CSPGs can enhance axon growth. In this report, we established an in vitro interface model of activated astrocytes and subsequently investigated gene delivery as a means to reduce CSPG levels and enhance axon growth. In the model, a continuous interface of CSPG producing astrocytes was created with neurons seeded opposite the astrocytes, and neurite crossing, stopping, and turning were evaluated as they approached the interface. We investigated the efficacy of lentiviral delivery to degrade or prevent the synthesis of CSPGs, thereby removing CSPG inhibition of neurite growth. Lentiviral delivery of RNAi targeting two key CSPG synthesis enzymes, chondroitin polymerizing factor and chondroitin synthase-1, decreased CSPGs, and reduced inhibition by the interface. Degradation of CSPGs by lentiviral delivery of chondroitinase also resulted in less inhibition and more neurites crossing the interface. These results indicate that the interface model provides a tool to investigate interventions that reduce inhibition by CSPGs, and that gene delivery can be effective in promoting neurite growth across an interface of CSPG producing astrocytes.

摘要

中枢神经系统损伤后,会形成神经胶质瘢痕,其在物理和生化上抑制轴突生长。在瘢痕中,活化的星形胶质细胞分泌抑制性细胞外基质,其中硫酸软骨素蛋白聚糖 (CSPGs) 被认为是主要的抑制性成分。CSPGs 在病变周围形成抑制性界面,阻止轴突穿过损伤部位,减少 CSPGs 可以促进轴突生长。在本报告中,我们建立了活化星形胶质细胞的体外界面模型,随后研究了基因传递作为降低 CSPG 水平和促进轴突生长的一种手段。在该模型中,在神经元种子对面培养星形胶质细胞,形成 CSPG 产生星形胶质细胞的连续界面,并评估神经元突起接近界面时的穿越、停止和转向。我们研究了慢病毒传递降解或防止 CSPG 合成的效果,从而消除 CSPG 对神经突生长的抑制作用。针对两个关键 CSPG 合成酶(软骨素聚合因子和软骨素合成酶-1)的 RNAi 的慢病毒传递降低了 CSPGs,并减少了界面的抑制作用。慢病毒传递软骨素酶降解 CSPGs 也导致更少的抑制和更多的神经突穿过界面。这些结果表明,该界面模型提供了一种工具来研究减少 CSPG 抑制的干预措施,并且基因传递可以有效地促进 CSPG 产生星形胶质细胞界面处的神经突生长。