IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-022-35574-x.html
   My bibliography  Save this article

Single-cell transcriptomic analysis reveals diversity within mammalian spinal motor neurons

Author

Listed:
  • Ee Shan Liau

    (National Defense Medical Center
    Academia Sinica)

  • Suoqin Jin

    (Wuhan University
    University of California, Irvine)

  • Yen-Chung Chen

    (Academia Sinica)

  • Wei-Szu Liu

    (Academia Sinica)

  • Maëliss Calon

    (Institut du Fer à Moulin
    UMR-S 1270
    Sorbonne Université)

  • Stéphane Nedelec

    (Institut du Fer à Moulin
    UMR-S 1270
    Sorbonne Université)

  • Qing Nie

    (University of California, Irvine
    University of California, Irvine)

  • Jun-An Chen

    (National Defense Medical Center
    Academia Sinica
    Academia Sinica)

Abstract

Spinal motor neurons (MNs) integrate sensory stimuli and brain commands to generate movements. In vertebrates, the molecular identities of the cardinal MN types such as those innervating limb versus trunk muscles are well elucidated. Yet the identities of finer subtypes within these cell populations that innervate individual muscle groups remain enigmatic. Here we investigate heterogeneity in mouse MNs using single-cell transcriptomics. Among limb-innervating MNs, we reveal a diverse neuropeptide code for delineating putative motor pool identities. Additionally, we uncover that axial MNs are subdivided into three molecularly distinct subtypes, defined by mediolaterally-biased Satb2, Nr2f2 or Bcl11b expression patterns with different axon guidance signatures. These three subtypes are present in chicken and human embryos, suggesting a conserved axial MN expression pattern across higher vertebrates. Overall, our study provides a molecular resource of spinal MN types and paves the way towards deciphering how neuronal subtypes evolved to accommodate vertebrate motor behaviors.

Suggested Citation

  • Ee Shan Liau & Suoqin Jin & Yen-Chung Chen & Wei-Szu Liu & Maëliss Calon & Stéphane Nedelec & Qing Nie & Jun-An Chen, 2023. "Single-cell transcriptomic analysis reveals diversity within mammalian spinal motor neurons," Nature Communications, Nature, vol. 14(1), pages 1-21, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-022-35574-x
    DOI: 10.1038/s41467-022-35574-x
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-022-35574-x
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-022-35574-x?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Tulsi Patel & Jennifer Hammelman & Siaresh Aziz & Sumin Jang & Michael Closser & Theodore L. Michaels & Jacob A. Blum & David K. Gifford & Hynek Wichterle, 2022. "Transcriptional dynamics of murine motor neuron maturation in vivo and in vitro," Nature Communications, Nature, vol. 13(1), pages 1-20, December.
    2. Daniel E. Russ & Ryan B. Patterson Cross & Li Li & Stephanie C. Koch & Kaya J. E. Matson & Archana Yadav & Mor R. Alkaslasi & Dylan I. Lee & Claire E. Le Pichon & Vilas Menon & Ariel J. Levine, 2021. "A harmonized atlas of mouse spinal cord cell types and their spatial organization," Nature Communications, Nature, vol. 12(1), pages 1-20, December.
    3. Jeffrey M. Perkel, 2021. "Single-cell analysis enters the multiomics age," Nature, Nature, vol. 595(7868), pages 614-616, July.
    Full references (including those not matched with items on IDEAS)

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Stanislav Tsitkov & Kelsey Valentine & Velina Kozareva & Aneesh Donde & Aaron Frank & Susan Lei & Jennifer Eyk & Steve Finkbeiner & Jeffrey D. Rothstein & Leslie M. Thompson & Dhruv Sareen & Clive N. , 2024. "Disease related changes in ATAC-seq of iPSC-derived motor neuron lines from ALS patients and controls," Nature Communications, Nature, vol. 15(1), pages 1-15, December.

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Kaya J. E. Matson & Daniel E. Russ & Claudia Kathe & Isabelle Hua & Dragan Maric & Yi Ding & Jonathan Krynitsky & Randall Pursley & Anupama Sathyamurthy & Jordan W. Squair & Boaz P. Levi & Gregoire Co, 2022. "Single cell atlas of spinal cord injury in mice reveals a pro-regenerative signature in spinocerebellar neurons," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    2. Charles Warwick & Joseph Salsovic & Junichi Hachisuka & Kelly M. Smith & Tayler D. Sheahan & Haichao Chen & James Ibinson & H. Richard Koerber & Sarah E. Ross, 2022. "Cell type-specific calcium imaging of central sensitization in mouse dorsal horn," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    3. Yongheng Fan & Xianming Wu & Sufang Han & Qi Zhang & Zheng Sun & Bing Chen & Xiaoyu Xue & Haipeng Zhang & Zhenni Chen & Man Yin & Zhifeng Xiao & Yannan Zhao & Jianwu Dai, 2023. "Single-cell analysis reveals region-heterogeneous responses in rhesus monkey spinal cord with complete injury," Nature Communications, Nature, vol. 14(1), pages 1-20, December.
    4. Shaojie Qin & Yi Zhang & Mingying Shi & Daiyu Miao & Jiansen Lu & Lu Wen & Yu Bai, 2024. "In-depth organic mass cytometry reveals differential contents of 3-hydroxybutanoic acid at the single-cell level," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
    5. JangKeun Kim & Braden T. Tierney & Eliah G. Overbey & Ezequiel Dantas & Matias Fuentealba & Jiwoon Park & S. Anand Narayanan & Fei Wu & Deena Najjar & Christopher R. Chin & Cem Meydan & Conor Loy & Be, 2024. "Single-cell multi-ome and immune profiles of the Inspiration4 crew reveal conserved, cell-type, and sex-specific responses to spaceflight," Nature Communications, Nature, vol. 15(1), pages 1-18, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-022-35574-x. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.