首页> 外文期刊>Nature >Two dynamically distinct circuits drive inhibition in the sensory thalamus
【24h】

Two dynamically distinct circuits drive inhibition in the sensory thalamus

机译:两个动态独特的电路驱动抑制在感官丘脑中

获取原文
获取原文并翻译 | 示例
       

摘要

Most sensory information destined for the neocortex is relayed through the thalamus, where considerable transformation occurs(1,2). One means of transformation involves interactions between excitatory thalamocortical neurons that carry data to the cortex and inhibitory neurons of the thalamic reticular nucleus (TRN) that regulate the flow of those data(3-6). Although the importance of the TRN has long been recognised(7-9), understanding of its cell types, their organization and their functional properties has lagged behind that of the thalamocortical systems they control. Here we address this by investigating the somatosensory and visual circuits of the TRN in mice. In the somatosensory TRN we observed two groups of genetically defined neurons that are topographically segregated and physiologically distinct, and that connect reciprocally with independent thalamocortical nuclei through dynamically divergent synapses. Calbindin-expressing cells-located in the central core-connect with the ventral posterior nucleus, the primary somatosensory thalamocortical relay. By contrast, somatostatin-expressing cells-which reside along the surrounding edges of the TRN-synapse with the posterior medial thalamic nucleus, a higher-order structure that carries both top-down and bottom-up information(10-12). The two TRN cell groups process their inputs in pathway-specific ways. Synapses from the ventral posterior nucleus to central TRN cells transmit rapid excitatory currents that depress deeply during repetitive activity, driving phasic spike output. Synapses from the posterior medial thalamic nucleus to edge TRN cells evoke slower, less depressing excitatory currents that drive more persistent spiking. Differences in the intrinsic physiology of TRN cell types, including state-dependent bursting, contribute to these output dynamics. The processing specializations of these two somatosensory TRN subcircuits therefore appear to be tuned to the signals they carry-a primary central subcircuit tuned to discrete sensory events, and a higher-order edge subcircuit tuned to temporally distributed signals integrated from multiple sources. The structure and function of visual TRN subcircuits closely resemble those of the somatosensory TRN. These results provide insights into how subnetworks of TRN neurons may differentially process distinct classes of thalamic information.In the thalamic reticular nucleus there are two neuron types that are segregated into central and edge zones and receive inputs from different thalamocortical nuclei, creating subcircuits with distinct dynamics.
机译:目的地用于新皮质的最具感官信息通过丘脑中继,其中发生了相当大的变换(1,2)。一种转化装置涉及兴奋性ThalamoCortical神经元之间的相互作用,其将数据携带到丘脑网状核(TRN)的皮质和抑制性神经元调节这些数据的流动(3-6)。虽然TRN的重要性长期以来(7-9),但对其细胞类型的理解,其组织及其功能性质的理解已经落后于他们控制的ThalamoCortical系统的背后。在这里,我们通过研究小鼠中Trn的躯体感觉和视觉电路来解决这一点。在躯体传感TRN中,我们观察到两组遗传定义的神经元,其拓扑地隔离和生理上截然不同,并且通过动态发散突触通过独立的Thalamicoctic核与互相连接。 Calbindin表达细胞位于中央核心与腹侧核,主要躯体传感型ThalamoMortical继电器。通过对比度,表达生长抑素表达细胞 - 沿着后内侧塔拉姆核的周围边缘居住,这是携带自上而下和自下而上信息(10-12)的高阶结构。两个TRN单元组以通路特定方式处理其输入。来自腹侧核与中央Trn细胞的突触传递快速兴奋性电流,在重复活动期间深深地抑制,驱动相位秒峰值输出。从后内侧肉豆蔻核到边缘Trn细胞的突触唤起较慢,较小的令人沮丧的兴奋性电流,驱动更持久的尖峰。 TRN小区类型的内在生理学的差异,包括状态依赖性突发,有助于这些输出动态。因此,这两个躯体传感TRN子电路的处理专业化似乎被调谐到它们携带到调谐到离散感官事件的主中央子电路的信号,以及调整到从多个源集成的时间分布信号的高阶边缘子电路。 Visual Trn Subcircuits的结构和功能非常类似于躯体传感TRN的结构。这些结果提供了Trn神经元的子网可以差异地处理不同类别的丘脑信息的洞察。在丘脑网状核中,有两个神经元类型被隔离成中央和边缘区域,并从不同的ThalamoCortical核接收输入,产生具有不同动态的子公司。

著录项

  • 来源
    《Nature》 |2020年第7818期|813-818|共6页
  • 作者单位

    Brown Univ Div Biol & Med Dept Neurosci Providence RI 02912 USA|Brown Univ Div Biol & Med Dept Mol Biol Cell Biol & Biochem Providence RI 02912 USA|Brown Univ Robert J & Nancy D Carney Inst Brain Sci Providence RI 02912 USA;

    Brown Univ Div Biol & Med Dept Neurosci Providence RI 02912 USA|NYU Ctr Neural Sci New York NY 10003 USA;

    Brown Univ Div Biol & Med Dept Neurosci Providence RI 02912 USA|Brown Univ Robert J & Nancy D Carney Inst Brain Sci Providence RI 02912 USA;

    Brown Univ Div Biol & Med Dept Neurosci Providence RI 02912 USA|Brown Univ Robert J & Nancy D Carney Inst Brain Sci Providence RI 02912 USA;

    Brown Univ Div Biol & Med Dept Neurosci Providence RI 02912 USA|Brown Univ Robert J & Nancy D Carney Inst Brain Sci Providence RI 02912 USA;

    Brown Univ Div Biol & Med Dept Neurosci Providence RI 02912 USA|Brown Univ Robert J & Nancy D Carney Inst Brain Sci Providence RI 02912 USA;

    Brown Univ Div Biol & Med Dept Neurosci Providence RI 02912 USA|Univ Alabama Birmingham UAB Civitan Int Res Ctr Birmingham AL 35294 USA|Univ Alabama Birmingham UAB Comprehens Neurosci Ctr Birmingham AL 35294 USA|Univ Alabama Birmingham Dept Neurobiol Birmingham AL 35294 USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 22:15:28

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号