• 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

尾壳核和伏隔核中直接和间接通路纹状体投射神经元树突棘的差异发育。

Differential Development of Dendritic Spines in Striatal Projection Neurons of Direct and Indirect Pathways in the Caudoputamen and Nucleus Accumbens.

机构信息

Institute of Anatomy and Cell Biology, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.

Institute of Neuroscience, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.

出版信息

eNeuro. 2023 Jun 12;10(6). doi: 10.1523/ENEURO.0366-22.2023. Print 2023 Jun.

DOI:10.1523/ENEURO.0366-22.2023
PMID:37253589
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10270317/
Abstract

Synaptic modification in postnatal development is essential for the maturation of neural networks. Developmental maturation of excitatory synapses occurs at the loci of dendritic spines that are dynamically regulated by growth and pruning. Striatal spiny projection neurons (SPNs) receive excitatory input from the cerebral cortex and thalamus. SPNs of the striatonigral direct pathway (dSPNs) and SPNs of the striatopallidal indirect pathway (iSPNs) have different developmental roots and functions. The spatial and temporal dynamics of dendritic spine maturation of these two types of SPNs remain elusive. Here, we delineate the developmental trajectories of dendritic spines of dSPNs and iSPNs in the caudoputamen and nucleus accumbens (NAc). We labeled dendritic spines of SPNs by microinjecting Cre-dependent AAV-eYFP viruses into newborn Drd1-Cre or Adora2a-Cre mice, and analyzed spinogenesis at three levels, including different SPN cell types, subregions and postnatal times. In the dorsolateral striatum, spine pruning of dSPNs and iSPNs occurred at postnatal day (P)30-P50. In the dorsomedial striatum, the spine density of both dSPNs and iSPNs reached its peak between P30 and P50, and spine pruning occurred after P30 and P50, respectively, for dSPNs and iSPNs. In the NAc shell, spines of dSPNs and iSPNs were pruned after P21-P30, but no significant pruning was observed in iSPNs of lateral NAc shell. In the NAc core, the spine density of dSPNs and iSPNs reached its peak at P21 and P30, respectively, and subsequently declined. Collectively, the developmental maturation of dendritic spines in dSPNs and iSPNs follows distinct spatiotemporal trajectories in the dorsal and ventral striatum.

摘要

出生后发育过程中的突触修饰对于神经网络的成熟至关重要。兴奋性突触的发育成熟发生在树突棘的位置,树突棘的生长和修剪受到动态调节。纹状体棘状投射神经元(SPNs)接收来自大脑皮层和丘脑的兴奋性输入。纹状体苍白球直接通路(dSPNs)和纹状体苍白球间接通路(iSPNs)的 SPNs 具有不同的发育根源和功能。这两种类型的 SPN 树突棘成熟的时空动态仍然难以捉摸。在这里,我们描绘了尾壳核和伏隔核(NAc)中 dSPNs 和 iSPNs 的树突棘发育轨迹。我们通过将 Cre 依赖性 AAV-eYFP 病毒微注射到新生的 Drd1-Cre 或 Adora2a-Cre 小鼠中,标记 SPN 的树突棘,并在三个水平上分析 spinogenesis,包括不同的 SPN 细胞类型、亚区和出生后时间。在背外侧纹状体中,dSPNs 和 iSPNs 的树突棘修剪发生在出生后第 30-50 天。在背内侧纹状体中,dSPNs 和 iSPNs 的树突棘密度在第 30-50 天之间达到峰值,dSPNs 和 iSPNs 的树突棘修剪分别发生在第 30 天和第 50 天之后。在 NAc 壳中,dSPNs 和 iSPNs 的树突棘在第 21-30 天之间修剪,但 lateral NAc 壳中的 iSPNs 没有观察到明显的修剪。在 NAc 核中,dSPNs 和 iSPNs 的树突棘密度分别在第 21 天和第 30 天达到峰值,随后下降。总之,dSPNs 和 iSPNs 树突棘的发育成熟在背侧和腹侧纹状体中遵循不同的时空轨迹。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bad/10270317/481f4779ea9e/ENEURO.0366-22.2023_f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bad/10270317/a866a842b438/ENEURO.0366-22.2023_f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bad/10270317/a814c8361803/ENEURO.0366-22.2023_f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bad/10270317/7916abc72508/ENEURO.0366-22.2023_f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bad/10270317/cde2021073de/ENEURO.0366-22.2023_f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bad/10270317/481f4779ea9e/ENEURO.0366-22.2023_f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bad/10270317/a866a842b438/ENEURO.0366-22.2023_f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bad/10270317/a814c8361803/ENEURO.0366-22.2023_f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bad/10270317/7916abc72508/ENEURO.0366-22.2023_f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bad/10270317/cde2021073de/ENEURO.0366-22.2023_f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bad/10270317/481f4779ea9e/ENEURO.0366-22.2023_f005.jpg

相似文献

1
Differential Development of Dendritic Spines in Striatal Projection Neurons of Direct and Indirect Pathways in the Caudoputamen and Nucleus Accumbens.尾壳核和伏隔核中直接和间接通路纹状体投射神经元树突棘的差异发育。
eNeuro. 2023 Jun 12;10(6). doi: 10.1523/ENEURO.0366-22.2023. Print 2023 Jun.
2
Pathway-Specific Remodeling of Thalamostriatal Synapses in a Mouse Model of Parkinson's Disease.帕金森病小鼠模型中丘脑纹状体突触的特定途径重塑。
Mov Disord. 2022 Jun;37(6):1164-1174. doi: 10.1002/mds.29030. Epub 2022 Apr 29.
3
Neuron type-specific proteomics reveals distinct Shank3 proteoforms in iSPNs and dSPNs lead to striatal synaptopathy in Shank3B mice.神经元类型特异性蛋白质组学揭示 iSPNs 和 dSPNs 中独特的 Shank3 蛋白形式,导致 Shank3B 小鼠纹状体突触病变。
Mol Psychiatry. 2024 Aug;29(8):2372-2388. doi: 10.1038/s41380-024-02493-w. Epub 2024 Mar 14.
4
Differential Synaptic Remodeling by Dopamine in Direct and Indirect Striatal Projection Neurons in Pitx3 Mice, a Genetic Model of Parkinson's Disease.帕金森病基因模型 Pitx3 小鼠中多巴胺对直接和间接纹状体投射神经元的突触重塑作用差异。
J Neurosci. 2018 Apr 11;38(15):3619-3630. doi: 10.1523/JNEUROSCI.3184-17.2018. Epub 2018 Feb 26.
5
A Population of Indirect Pathway Striatal Projection Neurons Is Selectively Entrained to Parkinsonian Beta Oscillations.一群间接通路纹状体投射神经元被选择性地锁定到帕金森病的β振荡。
J Neurosci. 2017 Oct 11;37(41):9977-9998. doi: 10.1523/JNEUROSCI.0658-17.2017. Epub 2017 Aug 28.
6
Comparison of unitary synaptic currents generated by indirect and direct pathway neurons of the mouse striatum.比较小鼠纹状体间接和直接通路神经元产生的单元突触电流。
J Neurophysiol. 2024 May 1;131(5):914-936. doi: 10.1152/jn.00066.2024. Epub 2024 Apr 10.
7
Pathway-specific dysregulation of striatal excitatory synapses by LRRK2 mutations.LRRK2 突变导致纹状体兴奋性突触的特定途径失调。
Elife. 2020 Oct 2;9:e58997. doi: 10.7554/eLife.58997.
8
Duration differences of corticostriatal responses in striatal projection neurons depend on calcium activated potassium currents.纹状体投射神经元皮质纹状体反应的持续时间差异取决于钙激活钾电流。
Front Syst Neurosci. 2013 Oct 4;7:63. doi: 10.3389/fnsys.2013.00063. eCollection 2013.
9
Differential organization of cortical inputs to striatal projection neurons of the matrix compartment in rats.大鼠纹状体基质区投射神经元皮质输入的差异组织
Front Syst Neurosci. 2015 Apr 14;9:51. doi: 10.3389/fnsys.2015.00051. eCollection 2015.
10
Striatal cell-type-specific molecular signatures reveal therapeutic targets in a model of dystonia.纹状体细胞类型特异性分子特征揭示了肌张力障碍模型中的治疗靶点。
bioRxiv. 2024 Oct 7:2024.10.07.617010. doi: 10.1101/2024.10.07.617010.

引用本文的文献

1
Development and cadherin-mediated control of prefrontal corticostriatal projections in mice.小鼠前额叶皮质纹状体投射的发育及钙黏蛋白介导的调控
iScience. 2023 Sep 22;26(10):108002. doi: 10.1016/j.isci.2023.108002. eCollection 2023 Oct 20.

本文引用的文献

1
Connectivity of the corticostriatal and thalamostriatal systems in normal and parkinsonian states: An update.皮质纹状体和丘脑纹状体系统在正常和帕金森状态下的连接:最新进展。
Neurobiol Dis. 2022 Nov;174:105878. doi: 10.1016/j.nbd.2022.105878. Epub 2022 Sep 29.
2
Prenatal immune stress blunts microglia reactivity, impairing neurocircuitry.产前免疫应激会使小胶质细胞反应迟钝,损害神经回路。
Nature. 2022 Oct;610(7931):327-334. doi: 10.1038/s41586-022-05274-z. Epub 2022 Sep 28.
3
Networking brainstem and basal ganglia circuits for movement.
用于运动的脑干和基底神经节回路的网络。
Nat Rev Neurosci. 2022 Jun;23(6):342-360. doi: 10.1038/s41583-022-00581-w. Epub 2022 Apr 14.
4
Projections from D2 Neurons in Different Subregions of Nucleus Accumbens Shell to Ventral Pallidum Play Distinct Roles in Reward and Aversion.伏隔核壳部不同亚区的 D2 神经元投射到腹侧苍白球在奖赏和厌恶中发挥不同作用。
Neurosci Bull. 2021 May;37(5):623-640. doi: 10.1007/s12264-021-00632-9. Epub 2021 Feb 6.
5
Opioid-induced structural and functional plasticity of medium-spiny neurons in the nucleus accumbens.阿肯伯氏核中中刺神经元的阿片类药物诱导的结构和功能可塑性。
Neurosci Biobehav Rev. 2021 Jan;120:417-430. doi: 10.1016/j.neubiorev.2020.10.015. Epub 2020 Nov 2.
6
Dendritic Spine Plasticity: Function and Mechanisms.树突棘可塑性:功能与机制
Front Synaptic Neurosci. 2020 Aug 28;12:36. doi: 10.3389/fnsyn.2020.00036. eCollection 2020.
7
Dendritic spine density is increased on nucleus accumbens D2 neurons after chronic social defeat.慢性社交挫败后,伏隔核 D2 神经元的树突棘密度增加。
Sci Rep. 2020 Jul 24;10(1):12393. doi: 10.1038/s41598-020-69339-7.
8
Dopamine D1 Receptors Regulate Spines in Striatal Direct-Pathway and Indirect-Pathway Neurons.多巴胺 D1 受体调节纹状体直接通路和间接通路神经元的棘突。
Mov Disord. 2020 Oct;35(10):1810-1821. doi: 10.1002/mds.28174. Epub 2020 Jul 9.
9
Brain-Wide Mapping of Afferent Inputs to Accumbens Nucleus Core Subdomains and Accumbens Nucleus Subnuclei.伏隔核核心亚区和伏隔核亚核传入输入的全脑图谱
Front Syst Neurosci. 2020 Mar 18;14:15. doi: 10.3389/fnsys.2020.00015. eCollection 2020.
10
Maturation of the microglial population varies across mesolimbic nuclei.小胶质细胞群体的成熟在中脑边缘核团中各不相同。
Eur J Neurosci. 2020 Oct;52(7):3689-3709. doi: 10.1111/ejn.14740. Epub 2020 May 11.