• 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

轴突转录因子在外周神经损伤中逆行信号转导。

Axonal transcription factors signal retrogradely in lesioned peripheral nerve.

机构信息

Department of Biological Chemistry, Weizmann Institute of Science, Rehovot, Israel.

出版信息

EMBO J. 2012 Mar 21;31(6):1350-63. doi: 10.1038/emboj.2011.494. Epub 2012 Jan 13.

DOI:10.1038/emboj.2011.494
PMID:22246183
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3321171/
Abstract

Retrograde axonal injury signalling stimulates cell body responses in lesioned peripheral neurons. The involvement of importins in retrograde transport suggests that transcription factors (TFs) might be directly involved in axonal injury signalling. Here, we show that multiple TFs are found in axons and associate with dynein in axoplasm from injured nerve. Biochemical and functional validation for one TF family establishes that axonal STAT3 is locally translated and activated upon injury, and is transported retrogradely with dynein and importin α5 to modulate survival of peripheral sensory neurons after injury. Hence, retrograde transport of TFs from axonal lesion sites provides a direct link between axon and nucleus.

摘要

逆行轴突损伤信号刺激受损外周神经元的细胞体反应。进口蛋白在逆行运输中的参与表明转录因子(TFs)可能直接参与轴突损伤信号。在这里,我们发现多个 TFs 存在于轴突中,并与损伤神经轴浆中的动力蛋白结合。对一个 TF 家族的生化和功能验证表明,轴突 STAT3 在损伤后局部翻译和激活,并与动力蛋白和 importin α5 一起逆行运输,以调节损伤后周围感觉神经元的存活。因此,TFs 从轴突损伤部位的逆行运输提供了轴突和核之间的直接联系。

相似文献

1
Axonal transcription factors signal retrogradely in lesioned peripheral nerve.轴突转录因子在外周神经损伤中逆行信号转导。
EMBO J. 2012 Mar 21;31(6):1350-63. doi: 10.1038/emboj.2011.494. Epub 2012 Jan 13.
2
Subcellular knockout of importin β1 perturbs axonal retrograde signaling.细胞质内敲除 importin β1 会扰乱轴突逆行信号转导。
Neuron. 2012 Jul 26;75(2):294-305. doi: 10.1016/j.neuron.2012.05.033.
3
Sensing nerve injury at the axonal ER: activated Luman/CREB3 serves as a novel axonally synthesized retrograde regeneration signal.在内质网处感知神经损伤:激活的Luman/CREB3作为一种新的轴突合成逆行再生信号。
Proc Natl Acad Sci U S A. 2014 Nov 11;111(45):16142-7. doi: 10.1073/pnas.1407462111. Epub 2014 Oct 27.
4
Localized regulation of axonal RanGTPase controls retrograde injury signaling in peripheral nerve.轴突 RanGTP 酶的局部调节控制周围神经中的逆行损伤信号传导。
Neuron. 2008 Jul 31;59(2):241-52. doi: 10.1016/j.neuron.2008.05.029.
5
Dual leucine zipper kinase is required for retrograde injury signaling and axonal regeneration.双亮氨酸拉链激酶是逆行损伤信号和轴突再生所必需的。
Neuron. 2012 Jun 21;74(6):1015-22. doi: 10.1016/j.neuron.2012.04.028.
6
Retrograde axonal transport of JNK signaling molecules influence injury induced nuclear changes in p-c-Jun and ATF3 in adult rat sensory neurons.JNK信号分子的逆行轴突运输影响成年大鼠感觉神经元中损伤诱导的p-c-Jun和ATF3的核变化。
Mol Cell Neurosci. 2005 Jun;29(2):269-82. doi: 10.1016/j.mcn.2005.03.002.
7
Ready, STAT, go: transcription factors on the move.准备,立即行动:活动的转录因子。
EMBO J. 2012 Mar 21;31(6):1331-3. doi: 10.1038/emboj.2012.34. Epub 2012 Feb 14.
8
Integration of retrograde axonal and nuclear transport mechanisms in neurons: implications for therapeutics.神经元中逆行轴突运输和核运输机制的整合:对治疗的启示。
Neuroscientist. 2004 Oct;10(5):404-8. doi: 10.1177/1073858404267884.
9
Axoplasmic importins enable retrograde injury signaling in lesioned nerve.轴浆输入蛋白可使受损神经发生逆行损伤信号传导。
Neuron. 2003 Dec 18;40(6):1095-104. doi: 10.1016/s0896-6273(03)00770-0.
10
Reactive oxygen species regulate axonal regeneration through the release of exosomal NADPH oxidase 2 complexes into injured axons.活性氧通过将外泌体 NADPH 氧化酶 2 复合物释放到损伤的轴突中,来调节轴突再生。
Nat Cell Biol. 2018 Mar;20(3):307-319. doi: 10.1038/s41556-018-0039-x. Epub 2018 Feb 12.

引用本文的文献

1
Mechanisms of Corneal Nerve Regeneration: Examining Molecular Regulators.角膜神经再生机制:探究分子调节因子
Cells. 2025 Aug 27;14(17):1322. doi: 10.3390/cells14171322.
2
Regulation of Subcellular Protein Synthesis for Restoring Neural Connectivity.用于恢复神经连接的亚细胞蛋白质合成调控
Int J Mol Sci. 2025 Jul 28;26(15):7283. doi: 10.3390/ijms26157283.
3
Deficiency in KPNA4, but Not in KPNA3, Causes Attention Deficit/Hyperactivity Disorder like Symptoms in Mice.KPNA4而非KPNA3的缺陷会导致小鼠出现类似注意力缺陷/多动障碍的症状。
Genes (Basel). 2025 Jun 6;16(6):690. doi: 10.3390/genes16060690.
4
Unravelling axonal transcriptional landscapes: insights from induced pluripotent stem cell-derived cortical neurons and implications for motor neuron degeneration.解析轴突转录图谱:来自诱导多能干细胞衍生的皮质神经元的见解及其对运动神经元变性的影响。
Open Biol. 2025 Jun;15(6):250101. doi: 10.1098/rsob.250101. Epub 2025 Jun 11.
5
Research status of regenerative difficulties after central nervous system injury.中枢神经系统损伤后再生困难的研究现状
Regen Ther. 2025 Apr 30;29:493-498. doi: 10.1016/j.reth.2025.04.011. eCollection 2025 Jun.
6
Direct observation of importin α family member KPNA1 in axonal transport with or without a schizophrenia-related mutation.直接观察输入蛋白α家族成员KPNA1在有无精神分裂症相关突变情况下的轴突运输。
J Biol Chem. 2025 Apr;301(4):108343. doi: 10.1016/j.jbc.2025.108343. Epub 2025 Feb 24.
7
The transcription factor combination MEF2 and KLF7 promotes axonal sprouting in the injured spinal cord with functional improvement and regeneration-associated gene expression.转录因子组合MEF2和KLF7可促进脊髓损伤后的轴突发芽,并改善功能以及促进与再生相关的基因表达。
Mol Neurodegener. 2025 Feb 8;20(1):18. doi: 10.1186/s13024-025-00805-4.
8
An Easy-to-Handle Route for Bicomponent Porous Tubes Fabrication as Nerve Guide Conduits.一种制备双组分多孔管作为神经导管的简便方法。
Polymers (Basel). 2024 Oct 14;16(20):2893. doi: 10.3390/polym16202893.
9
Cytokines reprogram airway sensory neurons in asthma.细胞因子可重编程哮喘患者气道感觉神经元。
bioRxiv. 2024 Sep 18:2023.01.26.525731. doi: 10.1101/2023.01.26.525731.
10
Autophagy-targeting modulation to promote peripheral nerve regeneration.靶向自噬调节以促进周围神经再生。
Neural Regen Res. 2025 Jul 1;20(7):1864-1882. doi: 10.4103/NRR.NRR-D-23-01948. Epub 2024 May 13.

本文引用的文献

1
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
Nuclear translocation of jacob in hippocampal neurons after stimuli inducing long-term potentiation but not long-term depression.刺激诱导长时程增强而不是长时程抑制后,海马神经元中 jacob 的核易位。
PLoS One. 2011 Feb 18;6(2):e17276. doi: 10.1371/journal.pone.0017276.
4
Transcriptome analysis of embryonic and adult sensory axons reveals changes in mRNA repertoire localization.胚胎和成年感觉轴突的转录组分析揭示了 mRNA 谱定位的变化。
RNA. 2011 Jan;17(1):85-98. doi: 10.1261/rna.2386111. Epub 2010 Nov 23.
5
Functions of Nogo proteins and their receptors in the nervous system.神经节苷脂蛋白及其受体在神经系统中的功能。
Nat Rev Neurosci. 2010 Dec;11(12):799-811. doi: 10.1038/nrn2936. Epub 2010 Nov 3.
6
Subcellular communication through RNA transport and localized protein synthesis.通过 RNA 运输和局部蛋白质合成进行细胞内通讯。
Traffic. 2010 Dec;11(12):1498-505. doi: 10.1111/j.1600-0854.2010.01118.x. Epub 2010 Oct 7.
7
Transcriptional profiling of intrinsic PNS factors in the postnatal mouse.在出生后小鼠中进行内在 PNS 因子的转录谱分析。
Mol Cell Neurosci. 2011 Jan;46(1):32-44. doi: 10.1016/j.mcn.2010.07.015. Epub 2010 Aug 7.
8
Signaling to transcription networks in the neuronal retrograde injury response.神经元逆行损伤反应中转录网络的信号转导。
Sci Signal. 2010 Jul 13;3(130):ra53. doi: 10.1126/scisignal.2000952.
9
Conserved 3'-untranslated region sequences direct subcellular localization of chaperone protein mRNAs in neurons.保守的 3'-非翻译区序列指导神经元中伴侣蛋白 mRNA 的亚细胞定位。
J Biol Chem. 2010 Jun 4;285(23):18025-38. doi: 10.1074/jbc.M109.061333. Epub 2010 Mar 22.
10
An NGF-responsive element targets myo-inositol monophosphatase-1 mRNA to sympathetic neuron axons.神经生长因子反应元件将肌醇单磷酸酶-1 mRNA 靶向至交感神经元轴突。
Nat Neurosci. 2010 Mar;13(3):291-301. doi: 10.1038/nn.2486. Epub 2010 Jan 31.