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

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 phy...

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Autores principales: Shah, Trishna, Leurgans, Sue E., Mehta, Rashi I., Yang, Jingyun, Galloway, Chad A., de Mesy Bentley, Karen L., Schneider, Julie A., Mehta, Rupal I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9728136/
https://www.ncbi.nlm.nih.gov/pubmed/36469302
http://dx.doi.org/10.1084/jem.20220618
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author Shah, Trishna
Leurgans, Sue E.
Mehta, Rashi I.
Yang, Jingyun
Galloway, Chad A.
de Mesy Bentley, Karen L.
Schneider, Julie A.
Mehta, Rupal I.
author_facet Shah, Trishna
Leurgans, Sue E.
Mehta, Rashi I.
Yang, Jingyun
Galloway, Chad A.
de Mesy Bentley, Karen L.
Schneider, Julie A.
Mehta, Rupal I.
author_sort Shah, Trishna
collection PubMed
description 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.
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spelling pubmed-97281362022-12-08 Arachnoid granulations are lymphatic conduits that communicate with bone marrow and dura-arachnoid stroma Shah, Trishna Leurgans, Sue E. Mehta, Rashi I. Yang, Jingyun Galloway, Chad A. de Mesy Bentley, Karen L. Schneider, Julie A. Mehta, Rupal I. J Exp Med Brief Definitive Report 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. Rockefeller University Press 2022-12-05 /pmc/articles/PMC9728136/ /pubmed/36469302 http://dx.doi.org/10.1084/jem.20220618 Text en © 2022 Shah et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Definitive Report
Shah, Trishna
Leurgans, Sue E.
Mehta, Rashi I.
Yang, Jingyun
Galloway, Chad A.
de Mesy Bentley, Karen L.
Schneider, Julie A.
Mehta, Rupal I.
Arachnoid granulations are lymphatic conduits that communicate with bone marrow and dura-arachnoid stroma
title Arachnoid granulations are lymphatic conduits that communicate with bone marrow and dura-arachnoid stroma
title_full Arachnoid granulations are lymphatic conduits that communicate with bone marrow and dura-arachnoid stroma
title_fullStr Arachnoid granulations are lymphatic conduits that communicate with bone marrow and dura-arachnoid stroma
title_full_unstemmed Arachnoid granulations are lymphatic conduits that communicate with bone marrow and dura-arachnoid stroma
title_short Arachnoid granulations are lymphatic conduits that communicate with bone marrow and dura-arachnoid stroma
title_sort arachnoid granulations are lymphatic conduits that communicate with bone marrow and dura-arachnoid stroma
topic Brief Definitive Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9728136/
https://www.ncbi.nlm.nih.gov/pubmed/36469302
http://dx.doi.org/10.1084/jem.20220618
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