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本文引用的文献

1
Prolonged human neural stem cell maturation supports recovery in injured rodent CNS.延长人类神经干细胞成熟时间有助于受损啮齿动物中枢神经系统的恢复。
J Clin Invest. 2017 Sep 1;127(9):3287-3299. doi: 10.1172/JCI92955. Epub 2017 Aug 21.
2
SOX9 Is an Astrocyte-Specific Nuclear Marker in the Adult Brain Outside the Neurogenic Regions.SOX9是成人大脑非神经发生区域中星形胶质细胞特异性核标记物。
J Neurosci. 2017 Apr 26;37(17):4493-4507. doi: 10.1523/JNEUROSCI.3199-16.2017. Epub 2017 Mar 23.
3
Preclinical Efficacy Failure of Human CNS-Derived Stem Cells for Use in the Pathway Study of Cervical Spinal Cord Injury.用于颈脊髓损伤通路研究的人中枢神经系统来源干细胞的临床前疗效失败
Stem Cell Reports. 2017 Feb 14;8(2):249-263. doi: 10.1016/j.stemcr.2016.12.018.
4
Ependymal cell contribution to scar formation after spinal cord injury is minimal, local and dependent on direct ependymal injury.室管膜细胞对脊髓损伤后瘢痕形成的贡献极小,局限于局部且依赖于直接的室管膜损伤。
Sci Rep. 2017 Jan 24;7:41122. doi: 10.1038/srep41122.
5
Glial progenitor cell-based treatment of the childhood leukodystrophies.基于神经胶质前体细胞的儿童脑白质营养不良治疗方法
Exp Neurol. 2016 Sep;283(Pt B):476-88. doi: 10.1016/j.expneurol.2016.05.010. Epub 2016 May 8.
6
Low excitatory innervation balances high intrinsic excitability of immature dentate neurons.低兴奋性神经支配平衡了未成熟齿状神经元的高内在兴奋性。
Nat Commun. 2016 Apr 20;7:11313. doi: 10.1038/ncomms11313.
7
Spinal cord reconstitution with homologous neural grafts enables robust corticospinal regeneration.用同源神经移植物进行脊髓重建可实现强大的皮质脊髓再生。
Nat Med. 2016 May;22(5):479-87. doi: 10.1038/nm.4066. Epub 2016 Mar 28.
8
The Scree Test For The Number Of Factors.因子数量的碎石检验
Multivariate Behav Res. 1966 Apr 1;1(2):245-76. doi: 10.1207/s15327906mbr0102_10.
9
A Unilateral Cervical Spinal Cord Contusion Injury Model in Non-Human Primates (Macaca mulatta).非人灵长类动物(猕猴)单侧颈脊髓挫伤损伤模型
J Neurotrauma. 2016 Mar 1;33(5):439-59. doi: 10.1089/neu.2015.3956. Epub 2016 Jan 20.
10
Restoration of skilled locomotion by sprouting corticospinal axons induced by co-deletion of PTEN and SOCS3.通过同时缺失PTEN和SOCS3诱导皮质脊髓轴突发芽来恢复熟练运动能力
Nat Commun. 2015 Nov 24;6:8074. doi: 10.1038/ncomms9074.

人神经干细胞移植对灵长类动物脊髓的修复作用。

Restorative effects of human neural stem cell grafts on the primate spinal cord.

机构信息

Department of Neurosciences, University of California, San Diego, La Jolla, California, USA.

Veterans Administration Medical Center, La Jolla, California, USA.

出版信息

Nat Med. 2018 May;24(4):484-490. doi: 10.1038/nm.4502. Epub 2018 Feb 26.

DOI:10.1038/nm.4502
PMID:29480894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5922761/
Abstract

We grafted human spinal cord-derived neural progenitor cells (NPCs) into sites of cervical spinal cord injury in rhesus monkeys (Macaca mulatta). Under three-drug immunosuppression, grafts survived at least 9 months postinjury and expressed both neuronal and glial markers. Monkey axons regenerated into grafts and formed synapses. Hundreds of thousands of human axons extended out from grafts through monkey white matter and synapsed in distal gray matter. Grafts gradually matured over 9 months and improved forelimb function beginning several months after grafting. These findings in a 'preclinical trial' support translation of NPC graft therapy to humans with the objective of reconstituting both a neuronal and glial milieu in the site of spinal cord injury.

摘要

我们将人脊髓源性神经前体细胞(NPCs)移植到恒河猴(Macaca mulatta)的颈脊髓损伤部位。在三种药物免疫抑制下,移植物在损伤后至少存活 9 个月,并表达神经元和神经胶质标志物。猴轴突再生到移植物中,并形成突触。数十万个人类轴突从移植物中穿过猴的白质延伸出来,并在远端灰质中形成突触。移植物在 9 个月内逐渐成熟,并在移植后数月开始改善前肢功能。这些在“临床前试验”中的发现支持将 NPC 移植疗法应用于人类,目的是在脊髓损伤部位重建神经元和神经胶质环境。