• 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

感觉神经元特化的分子相互作用。

Molecular interactions underlying the specification of sensory neurons.

机构信息

Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, 17177 Stockholm, Sweden.

出版信息

Trends Neurosci. 2012 Jun;35(6):373-81. doi: 10.1016/j.tins.2012.03.006. Epub 2012 Apr 18.

DOI:10.1016/j.tins.2012.03.006
PMID:22516617
Abstract

Sensory neurons of the dorsal root ganglion (DRG) respond to many different kinds of stimulus. The ability to discriminate between the diverse types of sensation is reflected by the existence of functionally and morphologically specialized sensory neurons. This neuronal diversity is created in a step-wise process extending well into postnatal life. Here, we review the hierarchical organization and the molecular process involving interactions between environmental growth factors, used and reused in different developmental contexts in self-reinforcing and cross-inhibitory mechanisms, and intrinsic gene programs that underlie the progressive diversification of sensory progenitors into specialized neurons. The recent advance in knowledge of sensory neuron specification may provide mechanistic principles that could extend to other parts of the nervous system.

摘要

背根神经节(DRG)的感觉神经元对许多不同类型的刺激做出反应。感觉神经元的功能和形态专门化的存在反映了它们能够区分不同类型的感觉。这种神经元多样性是通过一个逐步的过程产生的,这个过程一直延伸到出生后。在这里,我们回顾了涉及环境生长因子之间相互作用的分层组织和分子过程,这些生长因子在自我强化和交叉抑制机制以及内在基因程序中被重复使用,这些机制是感觉前体细胞逐渐分化为专门神经元的基础。最近在感觉神经元特化方面的知识进展可能为其他神经系统部分提供机制原则。

相似文献

1
Molecular interactions underlying the specification of sensory neurons.感觉神经元特化的分子相互作用。
Trends Neurosci. 2012 Jun;35(6):373-81. doi: 10.1016/j.tins.2012.03.006. Epub 2012 Apr 18.
2
Neurotrophin signalling and transcription programmes interactions in the development of somatosensory neurons.神经营养因子信号传导与转录程序在躯体感觉神经元发育中的相互作用。
Handb Exp Pharmacol. 2014;220:329-53. doi: 10.1007/978-3-642-45106-5_13.
3
Neuro-fuzzy decoding of sensory information from ensembles of simultaneously recorded dorsal root ganglion neurons for functional electrical stimulation applications.用于功能性电刺激应用的同时记录的背根神经节神经元集合的感觉信息的神经模糊解码。
J Neural Eng. 2011 Aug;8(4):046019. doi: 10.1088/1741-2560/8/4/046019. Epub 2011 Jun 23.
4
Neurochemical features of boar lumbosacral dorsal root ganglion neurons and characterization of sensory neurons innervating the urinary bladder trigone.猪腰荐背根神经节神经元的神经化学特征及膀胱三角感觉神经元的特性。
J Comp Neurol. 2013 Feb 1;521(2):342-66. doi: 10.1002/cne.23177.
5
Activation and circuitry of uterine-cervix-related neurons in the lumbosacral dorsal root ganglia and spinal cord at parturition.分娩时腰骶部背根神经节和脊髓中子宫-宫颈相关神经元的激活及神经回路
J Neurosci Res. 2005 Dec 15;82(6):875-89. doi: 10.1002/jnr.20690.
6
Effect of exposure to anti-NGF on sensory neurons of adult rats and guinea pigs.接触抗神经生长因子对成年大鼠和豚鼠感觉神经元的影响。
Brain Res. 1982 Jul 29;244(2):378-81. doi: 10.1016/0006-8993(82)90102-0.
7
Neurotrophins and the specification of neuronal phenotype.神经营养因子与神经元表型的特异性
Philos Trans R Soc Lond B Biol Sci. 1996 Mar 29;351(1338):405-11. doi: 10.1098/rstb.1996.0035.
8
Neural processing as causal inference.神经处理作为因果推理。
Curr Opin Neurobiol. 2011 Oct;21(5):774-81. doi: 10.1016/j.conb.2011.05.018.
9
Neurogenesis in postnatal mouse dorsal root ganglia.出生后小鼠背根神经节中的神经发生
Exp Neurol. 2001 Nov;172(1):60-9. doi: 10.1006/exnr.2001.7761.
10
Role of nerve growth factor in the adult dorsal root ganglia neuron and its response to injury.神经生长因子在成年背根神经节神经元中的作用及其对损伤的反应。
J Comp Neurol. 1984 Nov 20;230(1):110-8. doi: 10.1002/cne.902300110.

引用本文的文献

1
Induction of Human Pruriceptors from Pluripotent Stem Cells via Transcription Factors.通过转录因子从多能干细胞诱导生成人类瘙痒感受器
bioRxiv. 2025 Jun 15:2025.06.11.659208. doi: 10.1101/2025.06.11.659208.
2
Spatial organization, chromatin accessibility and gene-regulatory programs defining mouse sensory neurons.定义小鼠感觉神经元的空间组织、染色质可及性和基因调控程序。
Commun Biol. 2025 Jun 11;8(1):908. doi: 10.1038/s42003-025-08315-1.
3
Silicon Nanowire Mats Enable Advanced Bioelectrical Recordings in Primary DRG Cell Cultures.
硅纳米线垫可实现初级背根神经节细胞培养中的先进生物电记录。
Adv Healthc Mater. 2025 Jul;14(17):e2500379. doi: 10.1002/adhm.202500379. Epub 2025 May 24.
4
Generation of Neural Organoids and Their Application in Disease Modeling and Regenerative Medicine.神经类器官的生成及其在疾病建模和再生医学中的应用。
Adv Sci (Weinh). 2025 Aug;12(29):e01198. doi: 10.1002/advs.202501198. Epub 2025 May 24.
5
Genetics-Based Targeting Strategies for Precise Neuromodulation.基于遗传学的精确神经调节靶向策略。
Adv Sci (Weinh). 2025 Jul;12(28):e13817. doi: 10.1002/advs.202413817. Epub 2025 May 19.
6
Temporal refinement of Dach1 expression contributes to the development of somatosensory neurons.Dach1表达的时间性细化有助于体感神经元的发育。
EMBO J. 2025 May;44(10):2882-2905. doi: 10.1038/s44318-025-00427-y. Epub 2025 Apr 9.
7
Activity of spinal RORβ neurons is related to functional improvements following combination treatment after complete SCI.完全性脊髓损伤后联合治疗后,脊髓RORβ神经元的活性与功能改善有关。
Proc Natl Acad Sci U S A. 2025 Apr 15;122(15):e2406333122. doi: 10.1073/pnas.2406333122. Epub 2025 Apr 8.
8
Runx3, Brn3a and Isl1 interplay orchestrates the transcriptional program in the early stages of proprioceptive neuron development.Runx3、Brn3a和Isl1相互作用,在本体感觉神经元发育的早期阶段协调转录程序。
PLoS Genet. 2024 Dec 23;20(12):e1011401. doi: 10.1371/journal.pgen.1011401. eCollection 2024 Dec.
9
Involvement of HDAC2-mediated kcnq2/kcnq3 genes transcription repression activated by EREG/EGFR-ERK-Runx1 signaling in bone cancer pain.骨癌痛中由 EREG/EGFR-ERK-Runx1 信号激活的 HDAC2 介导的 kcnq2/kcnq3 基因转录抑制参与。
Cell Commun Signal. 2024 Aug 27;22(1):416. doi: 10.1186/s12964-024-01797-2.
10
Neph1 is required for neurite branching and is negatively regulated by the PRRXL1 homeodomain factor in the developing spinal cord dorsal horn.Neph1 对于神经突分支是必需的,并且在发育中的脊髓背角中受 PRRXL1 同源结构域因子的负调控。
Neural Dev. 2024 Jul 24;19(1):13. doi: 10.1186/s13064-024-00190-6.