Cerebrospinal fluid can exit into the skull bone marrow and instruct cranial hematopoiesis in mice with bacterial meningitis. Academic Article uri icon

Overview

abstract

  • Interactions between the immune and central nervous systems strongly influence brain health. Although the blood-brain barrier restricts this crosstalk, we now know that meningeal gateways through brain border tissues facilitate intersystem communication. Cerebrospinal fluid (CSF), which interfaces with the glymphatic system and thereby drains the brain's interstitial and perivascular spaces, facilitates outward signaling beyond the blood-brain barrier. In the present study, we report that CSF can exit into the skull bone marrow. Fluorescent tracers injected into the cisterna magna of mice migrate along perivascular spaces of dural blood vessels and then travel through hundreds of sub-millimeter skull channels into the calvarial marrow. During meningitis, bacteria hijack this route to invade the skull's hematopoietic niches and initiate cranial hematopoiesis ahead of remote tibial sites. As skull channels also directly provide leukocytes to meninges, the privileged sampling of brain-derived danger signals in CSF by regional marrow may have broad implications for inflammatory neurological disorders.

authors

  • Pulous, Fadi E
  • Cruz-Hernández, Jean C
  • Yang, Chongbo
  • Kaya, Ζeynep
  • Paccalet, Alexandre
  • Wojtkiewicz, Gregory
  • Capen, Diane
  • Brown, Dennis
  • Wu, Juwell W
  • Schloss, Maximilian J
  • Vinegoni, Claudio
  • Richter, Dmitry
  • Yamazoe, Masahiro
  • Hulsmans, Maarten
  • Momin, Noor
  • Grune, Jana
  • Rohde, David
  • McAlpine, Cameron S
  • Panizzi, Peter
  • Weissleder, Ralph
  • Kim, Dong-Eog
  • Swirski, Filip K
  • Lin, Charles P
  • Moskowitz, Michael A
  • Nahrendorf, Matthias

publication date

  • May 2, 2022

Research

keywords

  • Glymphatic System
  • Meningitis, Bacterial

Identity

PubMed Central ID

  • PMC9081225

Scopus Document Identifier

  • 85129174330

Digital Object Identifier (DOI)

  • 10.1038/s41593-022-01060-2

PubMed ID

  • 35501382

Additional Document Info

volume

  • 25

issue

  • 5