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A transcriptomic taxonomy of mouse brain-wide spinal projecting neurons

Author

Listed:
  • Carla C. Winter

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School
    PhD Program in Biological and Biomedical Sciences, Harvard Medical School)

  • Anne Jacobi

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School
    F. Hoffman-La Roche, pRED)

  • Junfeng Su

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Leeyup Chung

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Cindy T. J. van Velthoven

    (Allen Institute for Brain Science)

  • Zizhen Yao

    (Allen Institute for Brain Science)

  • Changkyu Lee

    (Allen Institute for Brain Science)

  • Zicong Zhang

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Shuguang Yu

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Kun Gao

    (University of California Los Angeles
    University of California Los Angeles)

  • Geraldine Duque Salazar

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Evgenii Kegeles

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School
    PhD Program in Biological and Biomedical Sciences, Harvard Medical School)

  • Yu Zhang

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Makenzie C. Tomihiro

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Yiming Zhang

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Zhiyun Yang

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Junjie Zhu

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Jing Tang

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Xuan Song

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Ryan J. Donahue

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

  • Qing Wang

    (University of California Los Angeles
    University of California Los Angeles)

  • Delissa McMillen

    (Allen Institute for Brain Science)

  • Michael Kunst

    (Allen Institute for Brain Science)

  • Ning Wang

    (Allen Institute for Brain Science)

  • Kimberly A. Smith

    (Allen Institute for Brain Science)

  • Gabriel E. Romero

    (Harvard Medical School)

  • Michelle M. Frank

    (Harvard Medical School)

  • Alexandra Krol

    (Massachusetts Institute of Technology)

  • Riki Kawaguchi

    (University of California Los Angeles
    University of California Los Angeles)

  • Daniel H. Geschwind

    (University of California Los Angeles
    University of California Los Angeles)

  • Guoping Feng

    (Massachusetts Institute of Technology)

  • Lisa V. Goodrich

    (Harvard Medical School)

  • Yuanyuan Liu

    (Somatosensation and Pain Unit, National Institute of Dental and Craniofacial Research, National Center for Complementary and Integrative Health, National Institutes of Health)

  • Bosiljka Tasic

    (Allen Institute for Brain Science)

  • Hongkui Zeng

    (Allen Institute for Brain Science)

  • Zhigang He

    (F. M. Kirby Neurobiology Center, Boston Children’s Hospital
    Harvard Medical School
    Harvard Medical School)

Abstract

The brain controls nearly all bodily functions via spinal projecting neurons (SPNs) that carry command signals from the brain to the spinal cord. However, a comprehensive molecular characterization of brain-wide SPNs is still lacking. Here we transcriptionally profiled a total of 65,002 SPNs, identified 76 region-specific SPN types, and mapped these types into a companion atlas of the whole mouse brain1. This taxonomy reveals a three-component organization of SPNs: (1) molecularly homogeneous excitatory SPNs from the cortex, red nucleus and cerebellum with somatotopic spinal terminations suitable for point-to-point communication; (2) heterogeneous populations in the reticular formation with broad spinal termination patterns, suitable for relaying commands related to the activities of the entire spinal cord; and (3) modulatory neurons expressing slow-acting neurotransmitters and/or neuropeptides in the hypothalamus, midbrain and reticular formation for ‘gain setting’ of brain–spinal signals. In addition, this atlas revealed a LIM homeobox transcription factor code that parcellates the reticulospinal neurons into five molecularly distinct and spatially segregated populations. Finally, we found transcriptional signatures of a subset of SPNs with large soma size and correlated these with fast-firing electrophysiological properties. Together, this study establishes a comprehensive taxonomy of brain-wide SPNs and provides insight into the functional organization of SPNs in mediating brain control of bodily functions.

Suggested Citation

  • Carla C. Winter & Anne Jacobi & Junfeng Su & Leeyup Chung & Cindy T. J. van Velthoven & Zizhen Yao & Changkyu Lee & Zicong Zhang & Shuguang Yu & Kun Gao & Geraldine Duque Salazar & Evgenii Kegeles & Y, 2023. "A transcriptomic taxonomy of mouse brain-wide spinal projecting neurons," Nature, Nature, vol. 624(7991), pages 403-414, December.
  • Handle: RePEc:nat:nature:v:624:y:2023:i:7991:d:10.1038_s41586-023-06817-8
    DOI: 10.1038/s41586-023-06817-8
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