| Literature DB >> 35501382 |
Fadi E Pulous1,2, Jean C Cruz-Hernández1,3, Chongbo Yang1,2, Ζeynep Kaya1,2, Alexandre Paccalet1,2, Gregory Wojtkiewicz1, Diane Capen4, Dennis Brown4, Juwell W Wu1,3, Maximilian J Schloss1,2, Claudio Vinegoni1,2, Dmitry Richter1,3, Masahiro Yamazoe1,2, Maarten Hulsmans1,2, Noor Momin1,2, Jana Grune1,2, David Rohde1,2, Cameron S McAlpine5,6, Peter Panizzi7, Ralph Weissleder1,2, Dong-Eog Kim8, Filip K Swirski5, Charles P Lin9,10, Michael A Moskowitz11,12,13, Matthias Nahrendorf14,15,16,17.
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.Entities:
Mesh:
Year: 2022 PMID: 35501382 PMCID: PMC9081225 DOI: 10.1038/s41593-022-01060-2
Source DB: PubMed Journal: Nat Neurosci ISSN: 1097-6256 Impact factor: 28.771