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本文引用的文献

1
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.
2
Neurotoxic reactive astrocytes are induced by activated microglia.神经毒性反应性星形胶质细胞由活化的小胶质细胞诱导产生。
Nature. 2017 Jan 26;541(7638):481-487. doi: 10.1038/nature21029. Epub 2017 Jan 18.
3
Contribution of propriospinal neurons to recovery of hand dexterity after corticospinal tract lesions in monkeys.脊髓固有神经元对猴子皮质脊髓束损伤后手灵活性恢复的作用。
Proc Natl Acad Sci U S A. 2017 Jan 17;114(3):604-609. doi: 10.1073/pnas.1610787114. Epub 2017 Jan 3.
4
Functional diversity of astrocytes in neural circuit regulation.星形胶质细胞在神经回路调节中的功能多样性。
Nat Rev Neurosci. 2017 Jan;18(1):31-41. doi: 10.1038/nrn.2016.159. Epub 2016 Dec 1.
5
Understanding the NG2 Glial Scar after Spinal Cord Injury.了解脊髓损伤后的NG2胶质瘢痕。
Front Neurol. 2016 Nov 15;7:199. doi: 10.3389/fneur.2016.00199. eCollection 2016.
6
Differential regenerative ability of sensory and motor neurons.感觉神经元和运动神经元的再生能力差异
Neurosci Lett. 2017 Jun 23;652:35-40. doi: 10.1016/j.neulet.2016.11.004. Epub 2016 Nov 3.
7
Injury-induced ctgfa directs glial bridging and spinal cord regeneration in zebrafish.损伤诱导的ctgfa指导斑马鱼的神经胶质桥接和脊髓再生。
Science. 2016 Nov 4;354(6312):630-634. doi: 10.1126/science.aaf2679.
8
Transplanted embryonic neurons integrate into adult neocortical circuits.移植的胚胎神经元整合到成年新皮层回路中。
Nature. 2016 Nov 10;539(7628):248-253. doi: 10.1038/nature20113. Epub 2016 Oct 26.
9
Neuropathic pain following traumatic spinal cord injury: Models, measurement, and mechanisms.创伤性脊髓损伤后的神经性疼痛:模型、测量与机制
J Neurosci Res. 2017 Jun;95(6):1295-1306. doi: 10.1002/jnr.23881. Epub 2016 Sep 12.
10
Enhancing neural activity to drive respiratory plasticity following cervical spinal cord injury.增强神经活动以驱动颈脊髓损伤后的呼吸可塑性。
Exp Neurol. 2017 Jan;287(Pt 2):276-287. doi: 10.1016/j.expneurol.2016.08.018. Epub 2016 Aug 28.

脊髓损伤与修复的细胞生物学

Cell biology of spinal cord injury and repair.

作者信息

O'Shea Timothy M, Burda Joshua E, Sofroniew Michael V

出版信息

J Clin Invest. 2017 Sep 1;127(9):3259-3270. doi: 10.1172/JCI90608. Epub 2017 Jul 24.

DOI:10.1172/JCI90608
PMID:28737515
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5669582/
Abstract

Spinal cord injury (SCI) lesions present diverse challenges for repair strategies. Anatomically complete injuries require restoration of neural connectivity across lesions. Anatomically incomplete injuries may benefit from augmentation of spontaneous circuit reorganization. Here, we review SCI cell biology, which varies considerably across three different lesion-related tissue compartments: (a) non-neural lesion core, (b) astrocyte scar border, and (c) surrounding spared but reactive neural tissue. After SCI, axon growth and circuit reorganization are determined by neuron-cell-autonomous mechanisms and by interactions among neurons, glia, and immune and other cells. These interactions are shaped by both the presence and the absence of growth-modulating molecules, which vary markedly in different lesion compartments. The emerging understanding of how SCI cell biology differs across lesion compartments is fundamental to developing rationally targeted repair strategies.

摘要

脊髓损伤(SCI)病变对修复策略提出了各种挑战。解剖学上完全性损伤需要恢复跨越病变部位的神经连接。解剖学上不完全性损伤可能受益于自发神经回路重组的增强。在此,我们综述脊髓损伤细胞生物学,其在三个不同的与病变相关的组织区域中差异很大:(a)非神经病变核心,(b)星形胶质瘢痕边界,以及(c)周围未受损但有反应的神经组织。脊髓损伤后,轴突生长和神经回路重组由神经元细胞自主机制以及神经元、神经胶质细胞、免疫细胞和其他细胞之间的相互作用决定。这些相互作用受到生长调节分子存在与否的影响,而生长调节分子在不同病变区域中差异显著。对于脊髓损伤细胞生物学在不同病变区域如何不同的新认识是制定合理靶向修复策略的基础。