猕猴视觉注意过程中小脑齿状神经元活动的编码。

IF 6.4 1区 生物学 Q1 BIOLOGY
eLife Pub Date : 2025-01-16 DOI:10.7554/eLife.99696
Nico A Flierman, Sue Ann Koay, Willem S van Hoogstraten, Tom J H Ruigrok, Pieter Roelfsema, Aleksandra Badura, Chris I De Zeeuw
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引用次数: 0

摘要

小脑在控制眼球运动中的作用已经得到了很好的证实,但它对更复杂形式的视觉行为的贡献仍然是难以捉摸的。为了研究视觉注意时小脑的活动,我们记录了两种非人灵长类动物(NHPs)齿状核(DN)神经元的细胞外活动。训练NHPs在保持注视中心的情况下读取外围视觉刺激指示的方向,并在延迟后通过向同一方向进行跳眼运动来报告线索的方向。我们发现单单元DN神经元在整个任务过程中调节峰值活动,并且它们的活动经常以一种异质性的方式连接暂时分离的试验内事件。为了更好地理解任务结构、行为表现和神经动力学之间的异质关系,我们构建了一个行为、编码和解码模型。两种NHPs表现出不同的行为策略,从而影响绩效。DN神经元的活动反映了独特的策略,视觉刺激的方向经常在即将到来的扫视之前被编码。此外,在表现较好的NHP中,DN神经元在视觉刺激后的上升活动潜伏期更短。在DN的记录位置用逆行示踪剂霍乱毒素B标记表明,这些神经元主要接受来自外侧小脑D1和D2区的浦肯野细胞以及主要的脑桥和内侧的神经元的输入,所有已知的区域都与前额叶皮层的神经元连接,参与扫视的规划。总之,我们的研究结果强调,在视觉注意任务中,DN神经元可以动态调节其活动,不仅包括感觉运动成分,还包括认知注意成分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Encoding of cerebellar dentate neuron activity during visual attention in rhesus macaques.

The role of cerebellum in controlling eye movements is well established, but its contribution to more complex forms of visual behavior has remained elusive. To study cerebellar activity during visual attention we recorded extracellular activity of dentate nucleus (DN) neurons in two non-human primates (NHPs). NHPs were trained to read the direction indicated by a peripheral visual stimulus while maintaining fixation at the center, and report the direction of the cue by performing a saccadic eye movement into the same direction following a delay. We found that single-unit DN neurons modulated spiking activity over the entire time course of the task, and that their activity often bridged temporally separated intra-trial events, yet in a heterogeneous manner. To better understand the heterogeneous relationship between task structure, behavioral performance, and neural dynamics, we constructed a behavioral, an encoding, and a decoding model. Both NHPs showed different behavioral strategies, which influenced the performance. Activity of the DN neurons reflected the unique strategies, with the direction of the visual stimulus frequently being encoded long before an upcoming saccade. Moreover, the latency of the ramping activity of DN neurons following presentation of the visual stimulus was shorter in the better performing NHP. Labeling with the retrograde tracer Cholera Toxin B in the recording location in the DN indicated that these neurons predominantly receive inputs from Purkinje cells in the D1 and D2 zones of the lateral cerebellum as well as neurons of the principal olive and medial pons, all regions known to connect with neurons in the prefrontal cortex contributing to planning of saccades. Together, our results highlight that DN neurons can dynamically modulate their activity during a visual attention task, comprising not only sensorimotor but also cognitive attentional components.

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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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