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本文引用的文献

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Axonal Localization of transgene mRNA in mature PNS and CNS neurons.转基因 mRNA 在成熟 PNS 和 CNS 神经元中的轴突定位。
J Neurosci. 2011 Oct 12;31(41):14481-7. doi: 10.1523/JNEUROSCI.2950-11.2011.
2
Limited availability of ZBP1 restricts axonal mRNA localization and nerve regeneration capacity.ZBP1 的有限可用性限制了轴突 mRNA 的定位和神经再生能力。
EMBO J. 2011 Sep 30;30(22):4665-77. doi: 10.1038/emboj.2011.347.
3
Sex differences in the effectiveness of treadmill training in enhancing axon regeneration in injured peripheral nerves.在促进损伤外周神经轴突再生方面,跑步机训练的有效性存在性别差异。
Dev Neurobiol. 2012 May;72(5):688-98. doi: 10.1002/dneu.20960.
4
Global deprivation of brain-derived neurotrophic factor in the CNS reveals an area-specific requirement for dendritic growth.中枢神经系统中脑源性神经营养因子的全球缺失揭示了树突生长的特定区域需求。
J Neurosci. 2010 Feb 3;30(5):1739-49. doi: 10.1523/JNEUROSCI.5100-09.2010.
5
Schwann cell influence on motor neuron regeneration accuracy.施万细胞对运动神经元再生准确性的影响。
Neuroscience. 2009 Sep 29;163(1):213-21. doi: 10.1016/j.neuroscience.2009.05.073. Epub 2009 Jun 6.
6
The role of neurotrophic factors in nerve regeneration.神经营养因子在神经再生中的作用。
Neurosurg Focus. 2009 Feb;26(2):E3. doi: 10.3171/FOC.2009.26.2.E3.
7
Single-neuron labeling with inducible Cre-mediated knockout in transgenic mice.在转基因小鼠中通过诱导型Cre介导的基因敲除进行单神经元标记。
Nat Neurosci. 2008 Jun;11(6):721-8. doi: 10.1038/nn.2118. Epub 2008 May 4.
8
Treadmill training promotes axon regeneration in injured peripheral nerves.跑步机训练可促进受损周围神经的轴突再生。
Exp Neurol. 2008 Jun;211(2):489-93. doi: 10.1016/j.expneurol.2008.02.013. Epub 2008 Mar 5.
9
Selective deletion of Bdnf in the ventromedial and dorsomedial hypothalamus of adult mice results in hyperphagic behavior and obesity.成年小鼠腹内侧和背内侧下丘脑的脑源性神经营养因子(Bdnf)被选择性敲除会导致摄食亢进行为和肥胖。
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10
A global double-fluorescent Cre reporter mouse.一种全球双荧光Cre报告基因小鼠。
Genesis. 2007 Sep;45(9):593-605. doi: 10.1002/dvg.20335.

BDNF 表达在神经元和雪旺细胞中的合作作用通过运动得到调节,从而促进神经再生。

Cooperative roles of BDNF expression in neurons and Schwann cells are modulated by exercise to facilitate nerve regeneration.

机构信息

Department of Cell Biology, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

出版信息

J Neurosci. 2012 Apr 4;32(14):5002-9. doi: 10.1523/JNEUROSCI.1411-11.2012.

DOI:10.1523/JNEUROSCI.1411-11.2012
PMID:22492055
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3382119/
Abstract

After peripheral nerve injury, neurotrophins play a key role in the regeneration of damaged axons that can be augmented by exercise, although the distinct roles played by neurons and Schwann cells are unclear. In this study, we evaluated the requirement for the neurotrophin, brain-derived neurotrophic factor (BDNF), in neurons and Schwann cells for the regeneration of peripheral axons after injury. Common fibular or tibial nerves in thy-1-YFP-H mice were cut bilaterally and repaired using a graft of the same nerve from transgenic mice lacking BDNF in Schwann cells (BDNF(-/-)) or wild-type mice (WT). Two weeks postrepair, axonal regeneration into BDNF(-/-) grafts was markedly less than WT grafts, emphasizing the importance of Schwann cell BDNF. Nerve regeneration was enhanced by treadmill training posttransection, regardless of the BDNF content of the nerve graft. We further tested the hypothesis that training-induced increases in BDNF in neurons allow regenerating axons to overcome a lack of BDNF expression in cells in the pathway through which they regenerate. Nerves in mice lacking BDNF in YFP(+) neurons (SLICK) were cut and repaired with BDNF(-/-) and WT nerves. SLICK axons lacking BDNF did not regenerate into grafts lacking Schwann cell BDNF. Treadmill training could not rescue the regeneration into BDNF(-/-) grafts if the neurons also lacked BDNF. Both Schwann cell- and neuron-derived BDNF are thus important for axon regeneration in cut peripheral nerves.

摘要

周围神经损伤后,神经营养因子在受损轴突的再生中发挥关键作用,运动可以增强这种作用,尽管神经元和施万细胞所发挥的作用尚不清楚。在这项研究中,我们评估了神经营养因子脑源性神经营养因子(BDNF)在神经元和施万细胞中的必要性,以促进损伤后周围轴突的再生。在 thy-1-YFP-H 小鼠的腓总神经或胫神经双侧切断后,使用缺乏施万细胞 BDNF(BDNF(-/-))或野生型(WT)小鼠的同种神经移植物进行修复。修复后 2 周,BDNF(-/-)移植物中的轴突再生明显少于 WT 移植物,这强调了施万细胞 BDNF 的重要性。无论神经移植物中的 BDNF 含量如何,横断后进行跑步机训练都能增强神经再生。我们进一步检验了一个假设,即训练诱导神经元中 BDNF 的增加使再生轴突能够克服其再生途径中细胞缺乏 BDNF 表达的问题。在 YFP(+)神经元中缺乏 BDNF 的小鼠(SLICK)的神经被切断并用 BDNF(-/-)和 WT 神经修复。缺乏 BDNF 的 SLICK 轴突不会再生到缺乏 Schwann 细胞 BDNF 的移植物中。如果神经元也缺乏 BDNF,跑步机训练则不能挽救 BDNF(-/-)移植物中的再生。因此,施万细胞和神经元来源的 BDNF 对切断的周围神经中的轴突再生都很重要。