Targeted micro-fiber arrays for measuring and manipulating localized multi-scale neural dynamics over large, deep brain volumes during behavior.

Targeted micro-fiber arrays for measuring and manipulating localized multi-scale neural dynamics over large, deep brain volumes during behavior.
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定向微纤维阵列,用于测量和操纵行为过程中大而深的大脑体积的局部多尺度神经动力学。

DOI:
10.1101/2023.11.17.567425
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发表时间:
2023
期刊:
bioRxiv : the preprint server for biology
影响因子:
--
通讯作者:
Howe,MarkW
Howe,MarkW
中科院分区:
--
文献类型:
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作者:
Vu,Mai-AnhT;Brown,EleanorH;Wen,MichelleJ;Noggle,ChristianA;Zhang,Zicheng;Monk,KevinJ;Bouabid,Safa;Mroz,Lydia;Graham,BenjaminM;Zhuo,Yizhou;Li,Yulong;Otchy,TimothyM;Tian,Lin;Davison,IanG;Boas,DavidA;Howe,MarkW

文献摘要

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Neural population dynamics relevant to behavior vary over multiple spatial and temporal scales across three-dimensional volumes. Current optical approaches lack the spatial coverage and resolution necessary to measure and manipulate naturally occurring patterns of large-scale, distributed dynamics within and across deep brain regions such as the striatum. We designed a new micro-fiber array approach capable of chronically measuring and optogenetically manipulating local dynamics across over 100 targeted locations simultaneously in head-fixed and freely moving mice, enabling the investigation of cell-type- and neurotransmitter-specific signals over arbitrary 3D volumes at a spatial resolution and coverage previously inaccessible. We applied this method to resolve rapid dopamine release dynamics across the striatum, revealing distinct, modality-specific spatiotemporal patterns in response to salient sensory stimuli extending over millimeters of tissue. Targeted optogenetics enabled flexible control of neural signaling on multiple spatial scales, better matching endogenous signaling patterns, and the spatial localization of behavioral function across large circuits.