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本文引用的文献

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Extracellular matrix regulation of inflammation in the healthy and injured spinal cord.健康和损伤脊髓中炎症的细胞外基质调节
Exp Neurol. 2014 Aug;258:24-34. doi: 10.1016/j.expneurol.2013.11.020.
2
Matrix metalloproteinases in inflammation.炎症中的基质金属蛋白酶
Biochim Biophys Acta. 2014 Aug;1840(8):2571-80. doi: 10.1016/j.bbagen.2014.03.007. Epub 2014 Mar 14.
3
Remyelination after spinal cord injury: is it a target for repair?脊髓损伤后的髓鞘修复:它是修复的靶点吗?
Prog Neurobiol. 2014 Jun;117:54-72. doi: 10.1016/j.pneurobio.2014.02.006. Epub 2014 Feb 28.
4
Matrix metalloproteinase 13 modulates intestinal epithelial barrier integrity in inflammatory diseases by activating TNF.基质金属蛋白酶 13 通过激活 TNF 调节炎症性疾病中的肠道上皮屏障完整性。
EMBO Mol Med. 2013 Jul;5(7):1000-16. doi: 10.1002/emmm.201202100. Epub 2013 May 30.
5
Growing the growth cone: remodeling the cytoskeleton to promote axon regeneration.生长锥的生长:重塑细胞骨架以促进轴突再生。
Trends Neurosci. 2012 Mar;35(3):164-74. doi: 10.1016/j.tins.2011.11.002. Epub 2011 Dec 5.
6
Integrin signaling, cell survival, and anoikis: distinctions, differences, and differentiation.整合素信号传导、细胞存活与失巢凋亡:区别、差异及分化
J Signal Transduct. 2011;2011:738137. doi: 10.1155/2011/738137. Epub 2011 Jul 13.
7
Trafficking and secretion of matrix metalloproteinase-2 in olfactory ensheathing glial cells: A role in cell migration?基质金属蛋白酶-2 在嗅鞘胶质细胞中的转运和分泌:在细胞迁移中起作用?
Glia. 2011 May;59(5):750-70. doi: 10.1002/glia.21146. Epub 2011 Feb 28.
8
Sustained delivery of activated Rho GTPases and BDNF promotes axon growth in CSPG-rich regions following spinal cord injury.持续递送激活的 Rho GTPases 和脑源性神经营养因子可促进脊髓损伤后富含 CSPG 的区域的轴突生长。
PLoS One. 2011 Jan 24;6(1):e16135. doi: 10.1371/journal.pone.0016135.
9
Hyaluronan fragments promote inflammation by down-regulating the anti-inflammatory A2a receptor.透明质酸片段通过下调抗炎 A2a 受体促进炎症。
Am J Respir Cell Mol Biol. 2011 Oct;45(4):675-83. doi: 10.1165/rcmb.2010-0387OC. Epub 2011 Jan 21.
10
Sympathetic neurons express and secrete MMP-2 and MT1-MMP to control nerve sprouting via pro-NGF conversion.交感神经元表达和分泌 MMP-2 和 MT1-MMP,通过前神经生长因子转化来控制神经发芽。
Cell Mol Neurobiol. 2011 Jan;31(1):17-25. doi: 10.1007/s10571-010-9548-2. Epub 2010 Aug 4.

[基质金属蛋白酶在轴突再生中的研究进展]

[Progress on matrix metalloproteinase in axonal regeneration].

作者信息

Li Yu-Ying, Ding Yue-Min, Zhang Xiong

机构信息

Zhejiang University School of Medcine,Hangzhou 310058,China.

School of Medicine, Zhejiang University City College, Hangzhou 310015, China.

出版信息

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2015 Jan;44(1):95-100. doi: 10.3785/j.issn.1008-9292.2015.01.016.

DOI:10.3785/j.issn.1008-9292.2015.01.016
PMID:25851983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10397019/
Abstract

Matrix metalloproteinases (MMPs) are zinc-dependent endopeptidases. MMPs can degrade and remodel extracellular matrix, also active or inactive many molecules attaching to matrix including receptors, growth factors and cytokines, so that injury-induced MMPs can change the extracellular environment to affect the axonal regeneration in central nervous system. In this review, with spinal cord injury (SCI) as an example we discuss the effects of MMPs on inflammation, neuronal viability, extracellular molecules, glial scar and axonal remyelination, which are all important to axonal regeneration.

摘要

基质金属蛋白酶(MMPs)是锌依赖性内肽酶。MMPs 能够降解并重塑细胞外基质,还能激活或失活许多附着于基质的分子,包括受体、生长因子和细胞因子,因此损伤诱导产生的 MMPs 可改变细胞外环境,从而影响中枢神经系统的轴突再生。在本综述中,我们以脊髓损伤(SCI)为例,探讨 MMPs 对炎症、神经元活力、细胞外分子、胶质瘢痕和轴突再髓鞘化的影响,这些均对轴突再生至关重要。