• 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

在一个有节奏的运动回路中,为可靠的生理学而构建的神经元形态。

Neuronal morphologies built for reliable physiology in a rhythmic motor circuit.

机构信息

Volen Center and Biology Department, Brandeis University, Waltham, United States.

Grass Laboratory, Marine Biological Laboratories, Woods Hole, United States.

出版信息

Elife. 2019 Jan 18;8:e41728. doi: 10.7554/eLife.41728.

DOI:10.7554/eLife.41728
PMID:30657452
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6349406/
Abstract

It is often assumed that highly-branched neuronal structures perform compartmentalized computations. However, previously we showed that the Gastric Mill (GM) neuron in the crustacean stomatogastric ganglion (STG) operates like a single electrotonic compartment, despite having thousands of branch points and total cable length >10 mm (Otopalik et al., 2017a; 2017b). Here we show that compact electrotonic architecture is generalizable to other STG neuron types, and that these neurons present direction-insensitive, linear voltage integration, suggesting they pool synaptic inputs across their neuronal structures. We also show, using simulations of 720 cable models spanning a broad range of geometries and passive properties, that compact electrotonus, linear integration, and directional insensitivity in STG neurons arise from their neurite geometries (diameters tapering from 10-20 µm to 2 µm at their terminal tips). A broad parameter search reveals multiple morphological and biophysical solutions for achieving different degrees of passive electrotonic decrement and computational strategies in the absence of active properties.

摘要

人们通常认为高度分支的神经元结构执行分区计算。然而,此前我们发现甲壳类动物口胃神经节(STG)中的胃磨(GM)神经元的运作方式类似于单个电紧张性隔室,尽管它有数千个分支点和总电缆长度>10 毫米(Otopalik 等人,2017a;2017b)。在这里,我们表明紧凑的电紧张性架构可推广到其他 STG 神经元类型,并且这些神经元呈现出方向不敏感的线性电压整合,这表明它们在神经元结构中汇集了突触输入。我们还通过模拟跨越广泛的几何形状和被动特性的 720 个电缆模型表明,STG 神经元中的紧凑电紧张、线性整合和方向不敏感源自它们的神经突几何形状(直径从 10-20 µm 逐渐变细到末端的 2 µm)。广泛的参数搜索揭示了多种形态和生物物理解决方案,可在没有主动特性的情况下实现不同程度的被动电紧张性衰减和计算策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/22ffc1fac0ae/elife-41728-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/859a5c34ff7d/elife-41728-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/8dfbcbbfe8e5/elife-41728-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/e1edd9da3fed/elife-41728-fig1-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/2daddd7a18b1/elife-41728-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/0a43fc73842d/elife-41728-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/335f895fbc1f/elife-41728-fig2-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/bd53ab081481/elife-41728-fig2-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/ff0e54e67c3d/elife-41728-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/5d1877ac7d62/elife-41728-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/de126fd8126e/elife-41728-fig3-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/3a52da44088d/elife-41728-fig3-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/03acabefb52a/elife-41728-fig3-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/d00b15b3b1e6/elife-41728-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/2015b04a6ff9/elife-41728-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/5c27abdb95c1/elife-41728-fig4-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/a3983faa661a/elife-41728-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/d41522e022b1/elife-41728-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/09e40619fedb/elife-41728-fig5-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/923b8cfb089c/elife-41728-fig5-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/f6431956ebd6/elife-41728-fig5-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/22ffc1fac0ae/elife-41728-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/859a5c34ff7d/elife-41728-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/8dfbcbbfe8e5/elife-41728-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/e1edd9da3fed/elife-41728-fig1-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/2daddd7a18b1/elife-41728-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/0a43fc73842d/elife-41728-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/335f895fbc1f/elife-41728-fig2-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/bd53ab081481/elife-41728-fig2-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/ff0e54e67c3d/elife-41728-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/5d1877ac7d62/elife-41728-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/de126fd8126e/elife-41728-fig3-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/3a52da44088d/elife-41728-fig3-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/03acabefb52a/elife-41728-fig3-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/d00b15b3b1e6/elife-41728-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/2015b04a6ff9/elife-41728-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/5c27abdb95c1/elife-41728-fig4-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/a3983faa661a/elife-41728-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/d41522e022b1/elife-41728-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/09e40619fedb/elife-41728-fig5-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/923b8cfb089c/elife-41728-fig5-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/f6431956ebd6/elife-41728-fig5-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6bb/6349406/22ffc1fac0ae/elife-41728-fig6.jpg

相似文献

1
Neuronal morphologies built for reliable physiology in a rhythmic motor circuit.在一个有节奏的运动回路中,为可靠的生理学而构建的神经元形态。
Elife. 2019 Jan 18;8:e41728. doi: 10.7554/eLife.41728.
2
When complex neuronal structures may not matter.当复杂的神经元结构可能无关紧要时。
Elife. 2017 Feb 6;6:e23508. doi: 10.7554/eLife.23508.
3
Actions of a histaminergic/peptidergic projection neuron on rhythmic motor patterns in the stomatogastric nervous system of the crab Cancer borealis.组胺能/肽能投射神经元对北方黄道蟹口胃神经系统节律性运动模式的作用。
J Comp Neurol. 2004 Feb 2;469(2):153-69. doi: 10.1002/cne.11003.
4
Recruitment of a projection neuron determines gastric mill motor pattern selection in the stomatogastric nervous system of the crab, Cancer borealis.投射神经元的募集决定了北方黄道蟹口胃神经系统中胃磨运动模式的选择。
J Neurophysiol. 1994 Oct;72(4):1451-63. doi: 10.1152/jn.1994.72.4.1451.
5
Anatomical Organization of Multiple Modulatory Inputs in a Rhythmic Motor System.节律性运动系统中多种调节性输入的解剖学组织
PLoS One. 2015 Nov 13;10(11):e0142956. doi: 10.1371/journal.pone.0142956. eCollection 2015.
6
Perturbation-specific responses by two neural circuits generating similar activity patterns.两种产生相似活动模式的神经回路的特异性扰动反应。
Curr Biol. 2021 Nov 8;31(21):4831-4838.e4. doi: 10.1016/j.cub.2021.08.042. Epub 2021 Sep 9.
7
Network feedback regulates motor output across a range of modulatory neuron activity.网络反馈在一系列调制神经元活动范围内调节运动输出。
J Neurophysiol. 2016 Jun 1;115(6):3249-63. doi: 10.1152/jn.01112.2015. Epub 2016 Mar 30.
8
Pyloric motor pattern modification by a newly identified projection neuron in the crab stomatogastric nervous system.蟹口胃神经系统中一种新发现的投射神经元对幽门运动模式的改变
J Neurophysiol. 1996 Jan;75(1):97-108. doi: 10.1152/jn.1996.75.1.97.
9
The Site of Spontaneous Ectopic Spike Initiation Facilitates Signal Integration in a Sensory Neuron.自发性异位峰电位起始位点促进感觉神经元中的信号整合。
J Neurosci. 2016 Jun 22;36(25):6718-31. doi: 10.1523/JNEUROSCI.2753-15.2016.
10
Divergent co-transmitter actions underlie motor pattern activation by a modulatory projection neuron.不同的共递质作用是调节性投射神经元激活运动模式的基础。
Eur J Neurosci. 2007 Sep;26(5):1148-65. doi: 10.1111/j.1460-9568.2007.05744.x.

引用本文的文献

1
Morphological variability may limit single-cell specificity to electric field stimulation.形态学变异性可能会限制电场刺激的单细胞特异性。
Front Synaptic Neurosci. 2025 Aug 5;17:1621352. doi: 10.3389/fnsyn.2025.1621352. eCollection 2025.
2
Distinct mechanisms underlie electrical coupling resonance and its interaction with membrane potential resonance.不同的机制是电耦合共振及其与膜电位共振相互作用的基础。
Front Syst Biol. 2023 Mar 8;3:1122433. doi: 10.3389/fsysb.2023.1122433. eCollection 2023.
3
The Effect of Doxapram on Proprioceptive Neurons: Invertebrate Model.

本文引用的文献

1
Differential processing in modality-specific Mauthner cell dendrites.模态特异性麦氏细胞树突的差异处理。
J Physiol. 2018 Feb 15;596(4):667-689. doi: 10.1113/JP274861. Epub 2017 Dec 18.
2
A balance of outward and linear inward ionic currents is required for generation of slow-wave oscillations.慢波振荡的产生需要外向和线性内向离子电流的平衡。
J Neurophysiol. 2017 Aug 1;118(2):1092-1104. doi: 10.1152/jn.00240.2017. Epub 2017 May 24.
3
Sloppy morphological tuning in identified neurons of the crustacean stomatogastric ganglion.
多沙普仑对本体感觉神经元的影响:无脊椎动物模型
NeuroSci. 2022 Oct 23;3(4):566-588. doi: 10.3390/neurosci3040041. eCollection 2022 Dec.
4
Morphology and synapse topography optimize linear encoding of synapse numbers in looming responsive descending neurons.形态学和突触拓扑结构优化了对逼近做出反应的下行神经元中突触数量的线性编码。
bioRxiv. 2024 Apr 28:2024.04.24.591016. doi: 10.1101/2024.04.24.591016.
5
Heterogeneous off-target impact of ion-channel deletion on intrinsic properties of hippocampal model neurons that self-regulate calcium.离子通道缺失对自我调节钙的海马体模型神经元内在特性的异质性脱靶影响。
Front Cell Neurosci. 2023 Oct 10;17:1241450. doi: 10.3389/fncel.2023.1241450. eCollection 2023.
6
Heterogeneous receptor expression underlies non-uniform peptidergic modulation of olfaction in Drosophila.异质受体表达是果蝇嗅觉中非均匀肽调制的基础。
Nat Commun. 2023 Aug 30;14(1):5280. doi: 10.1038/s41467-023-41012-3.
7
Neuronal morphology enhances robustness to perturbations of channel densities.神经元形态增强了对通道密度扰动的鲁棒性。
Proc Natl Acad Sci U S A. 2023 Feb 21;120(8):e2219049120. doi: 10.1073/pnas.2219049120. Epub 2023 Feb 14.
8
Periodicity Pitch Perception Part III: Sensibility and Pachinko Volatility.周期性音高感知第三部分:敏感性与弹珠机波动性
Front Neurosci. 2022 Mar 8;16:736642. doi: 10.3389/fnins.2022.736642. eCollection 2022.
9
The dynamic range of voltage-dependent gap junction signaling is maintained by -induced membrane potential depolarization.电压门控缝隙连接信号的动态范围由诱导的膜电位去极化维持。
J Neurophysiol. 2022 Mar 1;127(3):776-790. doi: 10.1152/jn.00545.2021. Epub 2022 Feb 16.
10
From the Neuroscience of Individual Variability to Climate Change.从个体差异的神经科学到气候变化。
J Neurosci. 2021 Dec 15;41(50):10213-10221. doi: 10.1523/JNEUROSCI.1261-21.2021. Epub 2021 Nov 9.
甲壳类动物口胃神经节中已鉴定神经元的形态学调谐不精确。
Elife. 2017 Feb 8;6:e22352. doi: 10.7554/eLife.22352.
4
When complex neuronal structures may not matter.当复杂的神经元结构可能无关紧要时。
Elife. 2017 Feb 6;6:e23508. doi: 10.7554/eLife.23508.
5
Cell dialysis by sharp electrodes can cause nonphysiological changes in neuron properties.通过尖锐电极进行细胞透析会导致神经元特性发生非生理性变化。
J Neurophysiol. 2015 Aug;114(2):1255-71. doi: 10.1152/jn.01010.2014. Epub 2015 Jun 10.
6
The role of linear and voltage-dependent ionic currents in the generation of slow wave oscillations.线性和电压依赖性离子电流在慢波振荡产生中的作用。
J Comput Neurosci. 2014 Oct;37(2):229-42. doi: 10.1007/s10827-014-0498-4. Epub 2014 Mar 27.
7
Five types of nonspiking interneurons in local pattern-generating circuits of the crayfish swimmeret system.五种非刺神经元在螯虾游泳足系统局部模式生成回路中的作用。
J Neurophysiol. 2013 Jul;110(2):344-57. doi: 10.1152/jn.00079.2013. Epub 2013 Apr 24.
8
Nonlinear dendritic processing determines angular tuning of barrel cortex neurons in vivo.非线性树突处理决定了活体桶状皮层神经元的角度调谐。
Nature. 2012 Oct 18;490(7420):397-401. doi: 10.1038/nature11451. Epub 2012 Sep 2.
9
TrakEM2 software for neural circuit reconstruction.TrakEM2 软件用于神经回路重建。
PLoS One. 2012;7(6):e38011. doi: 10.1371/journal.pone.0038011. Epub 2012 Jun 19.
10
Simple Neurite Tracer: open source software for reconstruction, visualization and analysis of neuronal processes.Simple Neurite Tracer:用于神经元过程重建、可视化和分析的开源软件。
Bioinformatics. 2011 Sep 1;27(17):2453-4. doi: 10.1093/bioinformatics/btr390. Epub 2011 Jul 4.