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Single-nucleus and spatial signatures of the brainstem in normal brain and mild traumatic brain injury in male mice

Author

Listed:
  • Yuan Zhuang

    (Capital Medical University)

  • Xixian Liao

    (Capital Medical University)

  • Fei Niu

    (Capital Medical University)

  • Ming Li

    (Capital Medical University)

  • Yu Yan

    (Capital Medical University)

  • Chuanhang He

    (Capital Medical University)

  • Xiang Wu

    (Shanghai Jiao Tong University)

  • Runfa Tian

    (Capital Medical University)

  • Guoyi Gao

    (Capital Medical University
    Capital Medical University)

Abstract

The mammalian brainstem is particularly vulnerable to mild traumatic brain injury (mTBI), which is associated with prolonged autonomic dysfunction and coma. The spatial cellular connections within the brainstem or the mechanisms underlying its response to injury have been underestimated. Here, we performed single-nucleus RNA sequencing with spatial transcriptome sequencing in both normal and mTBI brainstems in male mice, revealing thirty-five neuron and non-neuron clusters. Typically, we identified subtypes of neurons that co-release multiple neurotransmitters, especially in the sagittal midline of the brainstem. Spatially adjacent neurons sharing similar gene expression patterns. The brainstem’s response to mTBI has two features: (1) Oligodendrocytes around the fourth ventricle exhibit widespread disconnection at 1-h post-injury, and (2) Injury-related noradrenergic neurons, particularly in their interaction with neurons located in theIRt and the Sol. These findings provides a reference for further integrative investigations of cellular and circuit functions of brainstem.

Suggested Citation

  • Yuan Zhuang & Xixian Liao & Fei Niu & Ming Li & Yu Yan & Chuanhang He & Xiang Wu & Runfa Tian & Guoyi Gao, 2025. "Single-nucleus and spatial signatures of the brainstem in normal brain and mild traumatic brain injury in male mice," Nature Communications, Nature, vol. 16(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-59856-2
    DOI: 10.1038/s41467-025-59856-2
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