IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v640y2025i8058d10.1038_s41586-024-07765-7.html
   My bibliography  Save this article

Perisomatic ultrastructure efficiently classifies cells in mouse cortex

Author

Listed:
  • Leila Elabbady

    (Allen Institute for Brain Science
    University of Washington)

  • Sharmishtaa Seshamani

    (Allen Institute for Brain Science)

  • Shang Mu

    (Princeton University)

  • Gayathri Mahalingam

    (Allen Institute for Brain Science)

  • Casey M. Schneider-Mizell

    (Allen Institute for Brain Science)

  • Agnes L. Bodor

    (Allen Institute for Brain Science)

  • J. Alexander Bae

    (Princeton University)

  • Derrick Brittain

    (Allen Institute for Brain Science)

  • JoAnn Buchanan

    (Allen Institute for Brain Science)

  • Daniel J. Bumbarger

    (Allen Institute for Brain Science)

  • Manuel A. Castro

    (Princeton University)

  • Sven Dorkenwald

    (Allen Institute for Brain Science
    Princeton University)

  • Akhilesh Halageri

    (Princeton University)

  • Zhen Jia

    (Princeton University)

  • Chris Jordan

    (Princeton University)

  • Dan Kapner

    (Allen Institute for Brain Science)

  • Nico Kemnitz

    (Princeton University)

  • Sam Kinn

    (Allen Institute for Brain Science)

  • Kisuk Lee

    (Princeton University)

  • Kai Li

    (Princeton University)

  • Ran Lu

    (Princeton University)

  • Thomas Macrina

    (Princeton University)

  • Eric Mitchell

    (Princeton University)

  • Shanka Subhra Mondal

    (Princeton University)

  • Barak Nehoran

    (Princeton University)

  • Sergiy Popovych

    (Princeton University)

  • William Silversmith

    (Princeton University)

  • Marc Takeno

    (Allen Institute for Brain Science)

  • Russel Torres

    (Allen Institute for Brain Science)

  • Nicholas L. Turner

    (Princeton University)

  • William Wong

    (Princeton University)

  • Jingpeng Wu

    (Princeton University)

  • Wenjing Yin

    (Allen Institute for Brain Science)

  • Szi-chieh Yu

    (Princeton University)

  • H. Sebastian Seung

    (Princeton University)

  • R. Clay Reid

    (Allen Institute for Brain Science)

  • Nuno Maçarico Costa

    (Allen Institute for Brain Science)

  • Forrest Collman

    (Allen Institute for Brain Science)

Abstract

Mammalian neocortex contains a highly diverse set of cell types. These cell types have been mapped systematically using a variety of molecular, electrophysiological and morphological approaches1–4. Each modality offers new perspectives on the variation of biological processes underlying cell-type specialization. Cellular-scale electron microscopy provides dense ultrastructural examination and an unbiased perspective on the subcellular organization of brain cells, including their synaptic connectivity and nanometre-scale morphology. In data that contain tens of thousands of neurons, most of which have incomplete reconstructions, identifying cell types becomes a clear challenge for analysis5. Here, to address this challenge, we present a systematic survey of the somatic region of all cells in a cubic millimetre of cortex using quantitative features obtained from electron microscopy. This analysis demonstrates that the perisomatic region is sufficient to identify cell types, including types defined primarily on the basis of their connectivity patterns. We then describe how this classification facilitates cell-type-specific connectivity characterization and locating cells with rare connectivity patterns in the dataset.

Suggested Citation

  • Leila Elabbady & Sharmishtaa Seshamani & Shang Mu & Gayathri Mahalingam & Casey M. Schneider-Mizell & Agnes L. Bodor & J. Alexander Bae & Derrick Brittain & JoAnn Buchanan & Daniel J. Bumbarger & Manu, 2025. "Perisomatic ultrastructure efficiently classifies cells in mouse cortex," Nature, Nature, vol. 640(8058), pages 478-486, April.
  • Handle: RePEc:nat:nature:v:640:y:2025:i:8058:d:10.1038_s41586-024-07765-7
    DOI: 10.1038/s41586-024-07765-7
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41586-024-07765-7
    File Function: Abstract
    Download Restriction: Access to the full text of the articles in this series is restricted.

    File URL: https://libkey.io/10.1038/s41586-024-07765-7?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
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    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:nature:v:640:y:2025:i:8058:d:10.1038_s41586-024-07765-7. 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.

    We have no bibliographic references for this item. You can help adding them by using 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.