IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v639y2025i8056d10.1038_s41586-025-08589-9.html
   My bibliography  Save this article

Glycocalyx dysregulation impairs blood–brain barrier in ageing and disease

Author

Listed:
  • Sophia M. Shi

    (Stanford University
    Stanford University
    Stanford University School of Medicine
    Stanford University School of Medicine)

  • Ryan J. Suh

    (Stanford University School of Medicine
    Stanford University School of Medicine)

  • D. Judy Shon

    (Stanford University
    Stanford University)

  • Francisco J. Garcia

    (Picower Institute for Learning and Memory
    MIT)

  • Josephine K. Buff

    (Stanford University School of Medicine
    Stanford University School of Medicine)

  • Micaiah Atkins

    (Stanford University School of Medicine
    Stanford University School of Medicine
    Stanford University)

  • Lulin Li

    (Palo Alto Veterans Institute for Research)

  • Nannan Lu

    (Stanford University School of Medicine
    Stanford University School of Medicine)

  • Bryan Sun

    (Palo Alto Veterans Institute for Research)

  • Jian Luo

    (Palo Alto Veterans Institute for Research)

  • Ning-Sum To

    (Hong Kong Center for Neurodegenerative Diseases)

  • Tom H. Cheung

    (Hong Kong Center for Neurodegenerative Diseases
    The Hong Kong University of Science and Technology)

  • M. Windy McNerney

    (Stanford University School of Medicine
    Department of Veterans Affairs)

  • Myriam Heiman

    (Picower Institute for Learning and Memory
    MIT)

  • Carolyn R. Bertozzi

    (Stanford University
    Stanford University
    Stanford University)

  • Tony Wyss-Coray

    (Stanford University
    Stanford University School of Medicine
    Stanford University School of Medicine
    Stanford University)

Abstract

The blood–brain barrier (BBB) is highly specialized to protect the brain from harmful circulating factors in the blood and maintain brain homeostasis1,2. The brain endothelial glycocalyx layer, a carbohydrate-rich meshwork composed primarily of proteoglycans, glycoproteins and glycolipids that coats the BBB lumen, is a key structural component of the BBB3,4. This layer forms the first interface between the blood and brain vasculature, yet little is known about its composition and roles in supporting BBB function in homeostatic and diseased states. Here we find that the brain endothelial glycocalyx is highly dysregulated during ageing and neurodegenerative disease. We identify significant perturbation in an underexplored class of densely O-glycosylated proteins known as mucin-domain glycoproteins. We demonstrate that ageing- and disease-associated aberrations in brain endothelial mucin-domain glycoproteins lead to dysregulated BBB function and, in severe cases, brain haemorrhaging in mice. Finally, we demonstrate that we can improve BBB function and reduce neuroinflammation and cognitive deficits in aged mice by restoring core 1 mucin-type O-glycans to the brain endothelium using adeno-associated viruses. Cumulatively, our findings provide a detailed compositional and structural mapping of the ageing brain endothelial glycocalyx layer and reveal important consequences of ageing- and disease-associated glycocalyx dysregulation on BBB integrity and brain health.

Suggested Citation

  • Sophia M. Shi & Ryan J. Suh & D. Judy Shon & Francisco J. Garcia & Josephine K. Buff & Micaiah Atkins & Lulin Li & Nannan Lu & Bryan Sun & Jian Luo & Ning-Sum To & Tom H. Cheung & M. Windy McNerney & , 2025. "Glycocalyx dysregulation impairs blood–brain barrier in ageing and disease," Nature, Nature, vol. 639(8056), pages 985-994, March.
  • Handle: RePEc:nat:nature:v:639:y:2025:i:8056:d:10.1038_s41586-025-08589-9
    DOI: 10.1038/s41586-025-08589-9
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41586-025-08589-9
    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/s41586-025-08589-9?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:639:y:2025:i:8056:d:10.1038_s41586-025-08589-9. 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.