Glycocalyx dysregulation impairs blood–brain barrier in ageing and disease

The blood-brain barrier (BBB) is highly specialized to protect the brain from harmful circulating factors in the blood and maintain brain homeostasis<sup>1,2</sup>. 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 BBB<sup>3,4</sup>. 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.

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Publication Details

Journal
Nature
Published
2025-02-26
DOI
https://doi.org/10.1038/s41586-025-08589-9
Citations
82
Primary Topic
Barrier Structure and Function Studies
Type
article
Field-Weighted Citation Impact
69.06
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article

Glycocalyx dysregulation impairs blood–brain barrier in ageing and disease

Bryan Sun, M. Windy McNerney, Myriam Heiman, Tom H. Cheung et al.
82 citations
Nature
Barrier Structure and Function Studies
69.06
article

Glycocalyx dysregulation impairs blood–brain barrier in ageing and disease

Bryan Sun, M. Windy McNerney, Myriam Heiman, Tom H. Cheung, Nannan Lu, Tony Wyss‐Coray, F. García, Jian Luo, Micaiah Atkins, Carolyn R. Bertozzi, D. Judy Shon, Lulin Li, Ning-Sum To, Sophia Shi, Ryan J. Suh, Josephine K. Buff
article en
82 citations

Abstract

The blood-brain barrier (BBB) is highly specialized to protect the brain from harmful circulating factors in the blood and maintain brain homeostasis<sup>1,2</sup>. 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 BBB<sup>3,4</sup>. 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.

NatureVol. 639(8056)
Howard Hughes Medical Institute (US), Neurosciences Institute (US), Palo Alto Veterans Institute for Research (US), Stanford Health Care (US), Cell Technology (China) (HK), Mental Illness Research, Education and Clinical Centers (US), Stanford Medicine (US), Stanford University (US)
Openalex Percentile: Top 0%
Barrier Structure and Function Studies
69.06
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