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Identification of direct connections between the dura and the brain.
Smyth, Leon C D; Xu, Di; Okar, Serhat V; Dykstra, Taitea; Rustenhoven, Justin; Papadopoulos, Zachary; Bhasiin, Kesshni; Kim, Min Woo; Drieu, Antoine; Mamuladze, Tornike; Blackburn, Susan; Gu, Xingxing; Gaitán, María I; Nair, Govind; Storck, Steffen E; Du, Siling; White, Michael A; Bayguinov, Peter; Smirnov, Igor; Dikranian, Krikor; Reich, Daniel S; Kipnis, Jonathan.
Afiliação
  • Smyth LCD; Brain Immunology and Glia (BIG) Center, Washington University in St Louis, St Louis, MO, USA. l.c.smyth@wustl.edu.
  • Xu D; Department of Pathology and Immunology, School of Medicine, Washington University in St Louis, St Louis, MO, USA. l.c.smyth@wustl.edu.
  • Okar SV; Brain Immunology and Glia (BIG) Center, Washington University in St Louis, St Louis, MO, USA.
  • Dykstra T; Department of Pathology and Immunology, School of Medicine, Washington University in St Louis, St Louis, MO, USA.
  • Rustenhoven J; Translational Neuroradiology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
  • Papadopoulos Z; Brain Immunology and Glia (BIG) Center, Washington University in St Louis, St Louis, MO, USA.
  • Bhasiin K; Department of Pathology and Immunology, School of Medicine, Washington University in St Louis, St Louis, MO, USA.
  • Kim MW; Brain Immunology and Glia (BIG) Center, Washington University in St Louis, St Louis, MO, USA.
  • Drieu A; Department of Pathology and Immunology, School of Medicine, Washington University in St Louis, St Louis, MO, USA.
  • Mamuladze T; Department of Pharmacology and Clinical Pharmacology, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
  • Blackburn S; Centre for Brain Research, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
  • Gu X; Brain Immunology and Glia (BIG) Center, Washington University in St Louis, St Louis, MO, USA.
  • Gaitán MI; Department of Pathology and Immunology, School of Medicine, Washington University in St Louis, St Louis, MO, USA.
  • Nair G; Neuroscience Graduate Program, School of Medicine, Washington University in St Louis, St Louis, MO, USA.
  • Storck SE; Brain Immunology and Glia (BIG) Center, Washington University in St Louis, St Louis, MO, USA.
  • Du S; Department of Pathology and Immunology, School of Medicine, Washington University in St Louis, St Louis, MO, USA.
  • White MA; Brain Immunology and Glia (BIG) Center, Washington University in St Louis, St Louis, MO, USA.
  • Bayguinov P; Department of Pathology and Immunology, School of Medicine, Washington University in St Louis, St Louis, MO, USA.
  • Smirnov I; Immunology Graduate Program, School of Medicine, Washington University in St Louis, St Louis, MO, USA.
  • Dikranian K; Brain Immunology and Glia (BIG) Center, Washington University in St Louis, St Louis, MO, USA.
  • Reich DS; Department of Pathology and Immunology, School of Medicine, Washington University in St Louis, St Louis, MO, USA.
  • Kipnis J; Brain Immunology and Glia (BIG) Center, Washington University in St Louis, St Louis, MO, USA.
Nature ; 627(8002): 165-173, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38326613
ABSTRACT
The arachnoid barrier delineates the border between the central nervous system and dura mater. Although the arachnoid barrier creates a partition, communication between the central nervous system and the dura mater is crucial for waste clearance and immune surveillance1,2. How the arachnoid barrier balances separation and communication is poorly understood. Here, using transcriptomic data, we developed transgenic mice to examine specific anatomical structures that function as routes across the arachnoid barrier. Bridging veins create discontinuities where they cross the arachnoid barrier, forming structures that we termed arachnoid cuff exit (ACE) points. The openings that ACE points create allow the exchange of fluids and molecules between the subarachnoid space and the dura, enabling the drainage of cerebrospinal fluid and limited entry of molecules from the dura to the subarachnoid space. In healthy human volunteers, magnetic resonance imaging tracers transit along bridging veins in a similar manner to access the subarachnoid space. Notably, in neuroinflammatory conditions such as experimental autoimmune encephalomyelitis, ACE points also enable cellular trafficking, representing a route for immune cells to directly enter the subarachnoid space from the dura mater. Collectively, our results indicate that ACE points are a critical part of the anatomy of neuroimmune communication in both mice and humans that link the central nervous system with the dura and its immunological diversity and waste clearance systems.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aracnoide-Máter / Encéfalo / Dura-Máter Tipo de estudo: Diagnostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aracnoide-Máter / Encéfalo / Dura-Máter Tipo de estudo: Diagnostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article