{"title":"Single-cell reconstruction of whole-brain efferent projections from mouse ventral posteromedial thalamus.","authors":"Heng-Zheng Wei, Yi-Yao Li, Hong-Yi Jia, Tian-Yu Zhao, Xiao Ren, Xin-Tong Qiu, Fu-Xing Zhang, Yun-Qing Li, Ming-Ming Zhang","doi":"10.1186/s40708-026-00315-z","DOIUrl":null,"url":null,"abstract":"<p><p>The ventral posteromedial thalamic nucleus (VPM) relays orofacial somatosensory signals to the primary somatosensory cortex (SSp), yet its functional heterogeneity remains poorly defined at single-cell resolution. We combined fluorescence micro-optical sectioning tomography (fMOST) with single-neuron whole-brain reconstruction to map projections of vesicular glutamate transporter 2-positive (VGluT2⁺) excitatory neurons in the ventrolateral subdivision of VPM (vlVPM). Using 88 high-quality neurons with validated completeness, we identified pronounced structural heterogeneity and classified two clusters with distinct axonal profiles. Notably, we report two key findings that challenge the classical view: vlVPM neurons preferentially target superficial SSp layers (L1-3) rather than layer 4 (L4), and a multi-target subpopulation simultaneously innervates the motor cortex and basal ganglia via collaterals, establishing direct anatomical links to motor regulatory networks. These anatomical findings demonstrate that vlVPM establishes diverse projection pathways beyond canonical sensory relays, enabling direct structural crosstalk between sensory and motor circuits. This work provides a single-cell resolution framework for interpreting the anatomical basis of thalamic involvement in sensorimotor coordination.</p>","PeriodicalId":37465,"journal":{"name":"Brain Informatics","volume":" ","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2026-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13341580/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain Informatics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s40708-026-00315-z","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Computer Science","Score":null,"Total":0}
引用次数: 0
Abstract
The ventral posteromedial thalamic nucleus (VPM) relays orofacial somatosensory signals to the primary somatosensory cortex (SSp), yet its functional heterogeneity remains poorly defined at single-cell resolution. We combined fluorescence micro-optical sectioning tomography (fMOST) with single-neuron whole-brain reconstruction to map projections of vesicular glutamate transporter 2-positive (VGluT2⁺) excitatory neurons in the ventrolateral subdivision of VPM (vlVPM). Using 88 high-quality neurons with validated completeness, we identified pronounced structural heterogeneity and classified two clusters with distinct axonal profiles. Notably, we report two key findings that challenge the classical view: vlVPM neurons preferentially target superficial SSp layers (L1-3) rather than layer 4 (L4), and a multi-target subpopulation simultaneously innervates the motor cortex and basal ganglia via collaterals, establishing direct anatomical links to motor regulatory networks. These anatomical findings demonstrate that vlVPM establishes diverse projection pathways beyond canonical sensory relays, enabling direct structural crosstalk between sensory and motor circuits. This work provides a single-cell resolution framework for interpreting the anatomical basis of thalamic involvement in sensorimotor coordination.
期刊介绍:
Brain Informatics is an international, peer-reviewed, interdisciplinary open-access journal published under the brand SpringerOpen, which provides a unique platform for researchers and practitioners to disseminate original research on computational and informatics technologies related to brain. This journal addresses the computational, cognitive, physiological, biological, physical, ecological and social perspectives of brain informatics. It also welcomes emerging information technologies and advanced neuro-imaging technologies, such as big data analytics and interactive knowledge discovery related to various large-scale brain studies and their applications. This journal will publish high-quality original research papers, brief reports and critical reviews in all theoretical, technological, clinical and interdisciplinary studies that make up the field of brain informatics and its applications in brain-machine intelligence, brain-inspired intelligent systems, mental health and brain disorders, etc. The scope of papers includes the following five tracks: Track 1: Cognitive and Computational Foundations of Brain Science Track 2: Human Information Processing Systems Track 3: Brain Big Data Analytics, Curation and Management Track 4: Informatics Paradigms for Brain and Mental Health Research Track 5: Brain-Machine Intelligence and Brain-Inspired Computing