Whisking and locomotion are jointly represented in superior colliculus neurons.

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
PLoS Biology Pub Date : 2025-04-07 eCollection Date: 2025-04-01 DOI:10.1371/journal.pbio.3003087
Suma Chinta, Scott R Pluta
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引用次数: 0

Abstract

Active sensation requires the brain to interpret external stimuli against an ongoing estimate of body position. While internal estimates of body position are often ascribed to the cerebral cortex, we examined the midbrain superior colliculus (SC), due to its close relationship with the sensory periphery as well as higher, motor-related brain regions. Using high-density electrophysiology and movement tracking, we discovered that the on-going kinematics of whisker motion and locomotion speed accurately predict the firing rate of mouse SC neurons. Neural activity was best predicted by movements occurring either in the past, present, or future, indicating that the SC population continuously estimates a trajectory of self-motion. A combined representation of slow and fast whisking features predicted absolute whisker angle at high temporal resolution. Sensory reafference played at least a partial role in shaping this feature tuning. Taken together, these data indicate that the SC contains a joint representation of whisking and locomotor features that is potentially useful in guiding complex orienting movements involving the face and limbs.

拂动和运动在上丘神经元中共同表现。
主动感觉需要大脑根据对身体位置的持续估计来解释外部刺激。虽然身体位置的内部估计通常归因于大脑皮层,但我们检查了中脑上丘(SC),因为它与感觉外围以及更高的运动相关大脑区域密切相关。通过高密度电生理学和运动跟踪,我们发现,须运动和运动速度的持续运动学可以准确地预测小鼠SC神经元的放电速率。神经活动最好通过过去、现在或未来发生的运动来预测,这表明SC群体不断地估计自我运动的轨迹。慢速和快速晶须特征的组合表示在高时间分辨率下预测了绝对晶须角。感觉参考至少在形成这种特征调整方面发挥了部分作用。综上所述,这些数据表明,SC包含了快速运动和运动特征的联合表征,这在指导涉及面部和四肢的复杂定向运动方面可能很有用。
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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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