• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

受体酪氨酸激酶:调节中枢神经系统轴突再生的分子开关

Receptor tyrosine kinases: molecular switches regulating CNS axon regeneration.

作者信息

Vigneswara Vasanthy, Kundi Sarina, Ahmed Zubair

机构信息

Neuropharmacology and Neurobiology Section, School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.

出版信息

J Signal Transduct. 2012;2012:361721. doi: 10.1155/2012/361721. Epub 2012 Jul 16.

DOI:10.1155/2012/361721
PMID:22848811
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3405719/
Abstract

The poor or lack of injured adult central nervous system (CNS) axon regeneration results in devastating consequences and poor functional recovery. The interplay between the intrinsic and extrinsic factors contributes to robust inhibition of axon regeneration of injured CNS neurons. The insufficient or lack of trophic support for injured neurons is considered as one of the major obstacles contributing to their failure to survive and regrow their axons after injury. In the CNS, many of the signalling pathways associated with neuronal survival and axon regeneration are regulated by several classes of receptor tyrosine kinases (RTK) that respond to a variety of ligands. This paper highlights and summarises the most relevant recent findings pertinent to different classes of the RTK family of molecules, with a particular focus on elucidating their role in CNS axon regeneration.

摘要

成年中枢神经系统(CNS)轴突再生能力差或缺乏会导致灾难性后果和功能恢复不佳。内在因素和外在因素之间的相互作用对损伤的中枢神经系统神经元轴突再生产生强烈抑制作用。对损伤神经元的营养支持不足或缺乏被认为是导致其在损伤后无法存活和轴突再生的主要障碍之一。在中枢神经系统中,许多与神经元存活和轴突再生相关的信号通路由几类受体酪氨酸激酶(RTK)调节,这些受体酪氨酸激酶对多种配体作出反应。本文重点介绍和总结了与不同类别的RTK分子家族最相关的最新研究发现,特别关注阐明它们在中枢神经系统轴突再生中的作用。

相似文献

1
Receptor tyrosine kinases: molecular switches regulating CNS axon regeneration.受体酪氨酸激酶:调节中枢神经系统轴突再生的分子开关
J Signal Transduct. 2012;2012:361721. doi: 10.1155/2012/361721. Epub 2012 Jul 16.
2
Facilitating axon regeneration in the injured CNS by microtubules stabilization.通过微管稳定促进受损中枢神经系统中的轴突再生。
Commun Integr Biol. 2011 Jul;4(4):391-3. doi: 10.4161/cib.4.4.15552. Epub 2011 Jul 1.
3
The Virtuous Cycle of Axon Growth: Axonal Transport of Growth-Promoting Machinery as an Intrinsic Determinant of Axon Regeneration.轴突生长的良性循环:促进生长的机制的轴突运输作为轴突再生的内在决定因素。
Dev Neurobiol. 2018 Oct;78(10):898-925. doi: 10.1002/dneu.22608. Epub 2018 Jul 10.
4
Neuronal, but not glial, Contactin 2 negatively regulates axon regeneration in the injured adult optic nerve.神经元而非神经胶质的 Contactin 2 负向调节成年视神经损伤后的轴突再生。
Eur J Neurosci. 2021 Mar;53(6):1705-1721. doi: 10.1111/ejn.15121. Epub 2021 Mar 18.
5
Neuronal intrinsic barriers for axon regeneration in the adult CNS.成年中枢神经系统中轴突再生的神经元内在障碍。
Curr Opin Neurobiol. 2010 Aug;20(4):510-8. doi: 10.1016/j.conb.2010.03.013. Epub 2010 Apr 24.
6
Return of function after CNS axon regeneration: Lessons from injury-responsive intrinsically photosensitive and alpha retinal ganglion cells.中枢神经系统轴突再生后的功能恢复:损伤反应性固有光敏性和α视网膜神经节细胞的启示。
Prog Retin Eye Res. 2019 Jul;71:57-67. doi: 10.1016/j.preteyeres.2018.11.006. Epub 2018 Nov 17.
7
Mechanisms of Axon Elongation Following CNS Injury: What Is Happening at the Axon Tip?中枢神经系统损伤后轴突伸长的机制:轴突末端发生了什么?
Front Cell Neurosci. 2020 Jul 3;14:177. doi: 10.3389/fncel.2020.00177. eCollection 2020.
8
Learning to swim, again: Axon regeneration in fish.重新学习游泳:鱼类的轴突再生。
Exp Neurol. 2017 Jan;287(Pt 3):318-330. doi: 10.1016/j.expneurol.2016.02.022. Epub 2016 Mar 3.
9
The Role of Lipids, Lipid Metabolism and Ectopic Lipid Accumulation in Axon Growth, Regeneration and Repair after CNS Injury and Disease.脂质、脂代谢和异位脂质积累在中枢神经系统损伤和疾病后轴突生长、再生和修复中的作用。
Cells. 2021 May 1;10(5):1078. doi: 10.3390/cells10051078.
10
Gene Manipulation Strategies to Identify Molecular Regulators of Axon Regeneration in the Central Nervous System.用于鉴定中枢神经系统轴突再生分子调节因子的基因操作策略
Front Cell Neurosci. 2017 Aug 7;11:231. doi: 10.3389/fncel.2017.00231. eCollection 2017.

引用本文的文献

1
Potential Therapeutic Targets of Formononetin, a Type of Methoxylated Isoflavone, and Its Role in Cancer Therapy through the Modulation of Signal Transduction Pathways.芒柄花素作为一种甲氧基异黄酮的潜在治疗靶点及其通过调节信号转导通路在癌症治疗中的作用。
Int J Mol Sci. 2023 Jun 3;24(11):9719. doi: 10.3390/ijms24119719.
2
Osteoclast-derived extracellular vesicles are implicated in sensory neurons sprouting through the activation of epidermal growth factor signaling.破骨细胞衍生的细胞外囊泡通过激活表皮生长因子信号通路参与感觉神经元的发芽。
Cell Biosci. 2022 Aug 14;12(1):127. doi: 10.1186/s13578-022-00864-w.
3
Role of JAK2/STAT3 Signaling Pathway in the Tumorigenesis, Chemotherapy Resistance, and Treatment of Solid Tumors: A Systemic Review.

本文引用的文献

1
Neurotrophin signaling via long-distance axonal transport.通过长距离轴突运输的神经营养因子信号传导。
Annu Rev Phys Chem. 2012;63:571-94. doi: 10.1146/annurev-physchem-032511-143704. Epub 2012 Jan 30.
2
Activation of receptor protein-tyrosine kinases from the cytoplasmic compartment.细胞质受体蛋白酪氨酸激酶的激活。
J Biochem. 2012 Apr;151(4):353-9. doi: 10.1093/jb/mvs013. Epub 2012 Feb 17.
3
HB-EGF is necessary and sufficient for Müller glia dedifferentiation and retina regeneration.HB-EGF 对于 Müller 胶质细胞去分化和视网膜再生是必要且充分的。
JAK2/STAT3信号通路在实体瘤发生、化疗耐药及治疗中的作用:一项系统综述
J Inflamm Res. 2022 Feb 25;15:1349-1364. doi: 10.2147/JIR.S353489. eCollection 2022.
4
Beneficial Effects of Neurotrophin-4 Supplementation During Maturation of Porcine Cumulus-Oocyte Complexes and Subsequent Embryonic Development After Parthenogenetic Activation.神经营养因子-4补充对猪卵丘-卵母细胞复合体成熟及孤雌激活后胚胎发育的有益作用。
Front Vet Sci. 2021 Nov 12;8:779298. doi: 10.3389/fvets.2021.779298. eCollection 2021.
5
Extracellular and Intracellular Factors in Brain Cancer.脑癌中的细胞外和细胞内因素
Front Cell Dev Biol. 2021 Aug 27;9:699103. doi: 10.3389/fcell.2021.699103. eCollection 2021.
6
Analysis of Gene Expression and Neuronal Phenotype in Neuroscreen-1 (NS-1) Cells.神经筛选-1(NS-1)细胞中的基因表达与神经元表型分析
Int J Biomed Investig. 2018 Sep-Dec;1(3). Epub 2018 Dec 17.
7
High-throughput screen for compounds that modulate neurite growth of human induced pluripotent stem cell-derived neurons.高通量筛选化合物,调节人诱导多能干细胞源性神经元的神经突生长。
Dis Model Mech. 2018 Feb 2;11(2):dmm031906. doi: 10.1242/dmm.031906.
8
Axonal outgrowth, neuropeptides expression and receptors tyrosine kinase phosphorylation in 3D organotypic cultures of adult dorsal root ganglia.成年背根神经节三维器官型培养中的轴突生长、神经肽表达及受体酪氨酸激酶磷酸化
PLoS One. 2017 Jul 24;12(7):e0181612. doi: 10.1371/journal.pone.0181612. eCollection 2017.
Dev Cell. 2012 Feb 14;22(2):334-47. doi: 10.1016/j.devcel.2011.11.020.
4
Cross-talk between receptor tyrosine kinase and tumor necrosis factor-α signaling networks regulates apoptosis but not proliferation.受体酪氨酸激酶与肿瘤坏死因子-α信号网络的串扰调节细胞凋亡但不调节细胞增殖。
Mol Cell Proteomics. 2012 Jun;11(6):M111.013292. doi: 10.1074/mcp.M111.013292. Epub 2012 Feb 8.
5
GDNF-treated acellular nerve graft promotes motoneuron axon regeneration after implantation into cervical root avulsed spinal cord.胶质源性神经营养因子处理的去细胞神经移植物植入颈椎神经根撕脱脊髓后促进运动神经元轴突再生。
Neuropathol Appl Neurobiol. 2012 Dec;38(7):681-95. doi: 10.1111/j.1365-2990.2012.01253.x.
6
Role of mTOR in neuroprotection and axon regeneration after inflammatory stimulation.mTOR 在炎症刺激后的神经保护和轴突再生中的作用。
Neurobiol Dis. 2012 May;46(2):314-24. doi: 10.1016/j.nbd.2012.01.004. Epub 2012 Jan 20.
7
BDNF promotes EGF-induced proliferation and migration of human fetal neural stem/progenitor cells via the PI3K/Akt pathway.BDNF 通过 PI3K/Akt 通路促进 EGF 诱导的人胎脑神经干细胞/祖细胞的增殖和迁移。
Molecules. 2011 Dec 6;16(12):10146-56. doi: 10.3390/molecules161210146.
8
Oncomodulin affords limited regeneration to injured sensory axons in vitro and in vivo.Oncomodulin 可为体外和体内受损感觉轴突提供有限的再生。
Exp Neurol. 2012 Feb;233(2):708-16. doi: 10.1016/j.expneurol.2011.04.017. Epub 2011 Nov 10.
9
Transforming growth factor α transforms astrocytes to a growth-supportive phenotype after spinal cord injury.转化生长因子 α 在脊髓损伤后将星形胶质细胞转化为支持生长的表型。
J Neurosci. 2011 Oct 19;31(42):15173-87. doi: 10.1523/JNEUROSCI.3441-11.2011.
10
EphA4 blockers promote axonal regeneration and functional recovery following spinal cord injury in mice.EphA4 阻断剂促进小鼠脊髓损伤后的轴突再生和功能恢复。
PLoS One. 2011;6(9):e24636. doi: 10.1371/journal.pone.0024636. Epub 2011 Sep 13.