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Functional characterization of the dural sinuses as a neuroimmune interface
Author(s) -
Justin Rustenhoven,
Antoine Drieu,
Tornike Mamuladze,
Kalil Alves de Lima,
Taitea Dykstra,
Morgan Wall,
Zachary Papadopoulos,
Mitsuhiro Kanamori,
Andrea Francesca Salvador,
Wendy Baker,
Mackenzie Lemieux,
Sandro Dá Mesquita,
Andrea Cugurra,
James A. J. Fitzpatrick,
Sanja Sviben,
Ross G. Kossina,
Peter O. Bayguinov,
Reid Townsend,
Qiang Zhang,
Petra Erdmann-Gilmore,
Igor Smirnov,
M. Beatriz S. Lopes,
Jasmin Herz,
Jonathan Kipnis
Publication year - 2021
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2020.12.040
Subject(s) - meninges , biology , immune system , neuroscience , antigen , neuroinflammation , immunology , antigen presentation , cerebrospinal fluid , multiple sclerosis , neuroimmunology , immune privilege , central nervous system , pathology , inflammation , t cell , medicine
Despite the established dogma of central nervous system (CNS) immune privilege, neuroimmune interactions play an active role in diverse neurological disorders. However, the precise mechanisms underlying CNS immune surveillance remain elusive; particularly, the anatomical sites where peripheral adaptive immunity can sample CNS-derived antigens and the cellular and molecular mediators orchestrating this surveillance. Here, we demonstrate that CNS-derived antigens in the cerebrospinal fluid (CSF) accumulate around the dural sinuses, are captured by local antigen-presenting cells, and are presented to patrolling T cells. This surveillance is enabled by endothelial and mural cells forming the sinus stromal niche. T cell recognition of CSF-derived antigens at this site promoted tissue resident phenotypes and effector functions within the dural meninges. These findings highlight the critical role of dural sinuses as a neuroimmune interface, where brain antigens are surveyed under steady-state conditions, and shed light on age-related dysfunction and neuroinflammatory attack in animal models of multiple sclerosis.

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