| Literature DB >> 33508229 |
Justin Rustenhoven1, Antoine Drieu2, Tornike Mamuladze2, Kalil Alves de Lima2, Taitea Dykstra2, Morgan Wall3, Zachary Papadopoulos4, Mitsuhiro Kanamori2, Andrea Francesca Salvador5, Wendy Baker3, Mackenzie Lemieux6, Sandro Da Mesquita7, Andrea Cugurra8, James Fitzpatrick9, Sanja Sviben10, Ross Kossina10, Peter Bayguinov10, Reid R Townsend11, Qiang Zhang11, Petra Erdmann-Gilmore11, Igor Smirnov2, Maria-Beatriz Lopes12, Jasmin Herz2, Jonathan Kipnis13.
Abstract
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.Entities:
Keywords: CNS autoimmunity; CSF flow; antigen presentation; dura mater; meningeal immunity; meningeal lymphatics; meninges; neuroimmunology; sinus; stromal cells
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Year: 2021 PMID: 33508229 PMCID: PMC8487654 DOI: 10.1016/j.cell.2020.12.040
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582