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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2022
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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. |
format | Online Article Text |
id | pubmed-9728136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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