Arachnoid granulations are lymphatic conduits that communicate with bone marrow and dura-arachnoid stroma

Author:

Shah Trishna1ORCID,Leurgans Sue E.12ORCID,Mehta Rashi I.34ORCID,Yang Jingyun12ORCID,Galloway Chad A.5ORCID,de Mesy Bentley Karen L.5ORCID,Schneider Julie A.126ORCID,Mehta Rupal I.16ORCID

Affiliation:

1. Rush Alzheimer’s Disease Center, Rush University Medical Center, Chicago, IL 1

2. Department of Neurological Sciences, Rush University Medical Center, Chicago, IL 2

3. Department of Neuroradiology, Rockefeller Neuroscience Institute, West Virginia University, Morgantown, WV 3

4. Department of Neuroscience, Rockefeller Neuroscience Institute, West Virginia University, Morgantown, WV 4

5. Department of Pathology, University of Rochester Medical Center, Rochester, NY 5

6. Department of Pathology, Rush University Medical Center, Chicago, IL 6

Abstract

Arachnoid granulations (AG) are poorly investigated. Historical reports suggest that they regulate brain volume by passively transporting cerebrospinal fluid (CSF) into dural venous sinuses. Here, we studied the microstructure of cerebral AG in humans with the aim of understanding their roles in physiology. We discovered marked variations in AG size, lobation, location, content, and degree of surface encapsulation. High-resolution microscopy shows that AG consist of outer capsule and inner stromal core regions. The fine and porous framework suggests uncharacterized functions of AG in mechanical CSF filtration. Moreover, internal cytokine and immune cell enrichment imply unexplored neuroimmune properties of these structures that localize to the brain–meningeal lymphatic interface. Dramatic age-associated changes in AG structure are additionally identified. This study depicts for the first time microscopic networks of internal channels that communicate with perisinus spaces, suggesting that AG subserve important functions as transarachnoidal flow passageways. These data raise new theories regarding glymphatic–lymphatic coupling and mechanisms of CSF antigen clearance, homeostasis, and diseases.

Funder

National Institutes of Health

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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