直接和间接通路纹状体投射神经元的动态集合平衡是决策相关行动选择的基础

IF 7.5 1区 生物学 Q1 CELL BIOLOGY Cell reports Pub Date : 2024-09-13 DOI:10.1016/j.celrep.2024.114726
Shunhang Tang, Lele Cui, Jingwei Pan, Ning-long Xu
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引用次数: 0

摘要

背侧纹状体后部(pDS)在感觉引导的决策中扮演着至关重要的角色。然而,目前仍不清楚拮抗的直接和间接通路纹状体投射神经元(dSPNs 和 iSPNs)是如何协同工作以支持行动选择的。在此,我们采用深脑双光子成像技术研究了听觉引导决策任务中特定通路的单神经元和群体表征。我们发现,大多数 pDS 投射神经元主要编码选择信息。dSPNs和iSPNs都由大小相当的不同亚群组成,代表相互竞争的选择,从而在两种通路之间实现了多集合平衡。耐人寻味的是,这种集合平衡在决策期会出现动态变化:dSPNs 对逆向选择的偏好明显强于 iSPNs。这种动态转变进一步体现在神经元间的协同活动和群体轨迹的发散上。我们的研究结果支持平衡转移模型,该模型是一种神经元群机制,协调直接和间接纹状体通路,在决策过程中诱发选定的行动。
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Dynamic ensemble balance in direct- and indirect-pathway striatal projection neurons underlying decision-related action selection

The posterior dorsal striatum (pDS) plays an essential role in sensory-guided decision-making. However, it remains unclear how the antagonizing direct- and indirect-pathway striatal projection neurons (dSPNs and iSPNs) work in concert to support action selection. Here, we employed deep-brain two-photon imaging to investigate pathway-specific single-neuron and population representations during an auditory-guided decision-making task. We found that the majority of pDS projection neurons predominantly encode choice information. Both dSPNs and iSPNs comprise divergent subpopulations of comparable sizes representing competing choices, rendering a multi-ensemble balance between the two pathways. Intriguingly, such ensemble balance displays a dynamic shift during the decision period: dSPNs show a significantly stronger preference for the contraversive choice than iSPNs. This dynamic shift is further manifested in the inter-neuronal coactivity and population trajectory divergence. Our results support a balance-shift model as a neuronal population mechanism coordinating the direct and indirect striatal pathways for eliciting selected actions during decision-making.

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来源期刊
Cell reports
Cell reports CELL BIOLOGY-
CiteScore
13.80
自引率
1.10%
发文量
1305
审稿时长
77 days
期刊介绍: Cell Reports publishes high-quality research across the life sciences and focuses on new biological insight as its primary criterion for publication. The journal offers three primary article types: Reports, which are shorter single-point articles, research articles, which are longer and provide deeper mechanistic insights, and resources, which highlight significant technical advances or major informational datasets that contribute to biological advances. Reviews covering recent literature in emerging and active fields are also accepted. The Cell Reports Portfolio includes gold open-access journals that cover life, medical, and physical sciences, and its mission is to make cutting-edge research and methodologies available to a wide readership. The journal's professional in-house editors work closely with authors, reviewers, and the scientific advisory board, which consists of current and future leaders in their respective fields. The advisory board guides the scope, content, and quality of the journal, but editorial decisions are independently made by the in-house scientific editors of Cell Reports.
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