Literature DB >> 34083450

Heterogeneity of meningeal B cells reveals a lymphopoietic niche at the CNS borders.

Simone Brioschi1, Wei-Le Wang1, Vincent Peng1, Meng Wang2, Irina Shchukina1, Zev J Greenberg3, Jennifer K Bando4, Natalia Jaeger1, Rafael S Czepielewski1, Amanda Swain1, Denis A Mogilenko1, Wandy L Beatty5, Peter Bayguinov6, James A J Fitzpatrick6,7,8, Laura G Schuettpelz3, Catrina C Fronick9, Igor Smirnov1, Jonathan Kipnis1, Virginia S Shapiro10, Gregory F Wu11, Susan Gilfillan1, Marina Cella1, Maxim N Artyomov1, Steven H Kleinstein2,12, Marco Colonna13.   

Abstract

The meninges contain adaptive immune cells that provide immunosurveillance of the central nervous system (CNS). These cells are thought to derive from the systemic circulation. Through single-cell analyses, confocal imaging, bone marrow chimeras, and parabiosis experiments, we show that meningeal B cells derive locally from the calvaria, which harbors a bone marrow niche for hematopoiesis. B cells reach the meninges from the calvaria through specialized vascular connections. This calvarial-meningeal path of B cell development may provide the CNS with a constant supply of B cells educated by CNS antigens. Conversely, we show that a subset of antigen-experienced B cells that populate the meninges in aging mice are blood-borne. These results identify a private source for meningeal B cells, which may help maintain immune privilege within the CNS.
Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

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Year:  2021        PMID: 34083450      PMCID: PMC8448524          DOI: 10.1126/science.abf9277

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   63.714


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