TY - JOUR
T1 - Extrasinusoidal macrophages are a distinct subset of immunologically active dural macrophages
AU - Amann, Lukas
AU - Fell, Amelie
AU - Monaco, Gianni
AU - Sankowski, Roman
AU - Wu, Huang Zie Quann
AU - Jordão, Marta Joana Costa
AU - Borst, Katharina
AU - Fliegauf, Maximilian
AU - Masuda, Takahiro
AU - Ardura-Fabregat, Alberto
AU - Paterson, Neil
AU - Nent, Elisa
AU - Cook, James
AU - Staszewski, Ori
AU - Mossad, Omar
AU - Falk, Thorsten
AU - Louveau, Antoine
AU - Smirnov, Igor
AU - Kipnis, Jonathan
AU - Lämmermann, Tim
AU - Prinz, Marco
N1 - Publisher Copyright:
© 2024 American Association for the Advancement of Science. All rights reserved.
PY - 2024/12
Y1 - 2024/12
N2 - Although macrophages in the meningeal compartments of the central nervous system (CNS) have been comprehensively characterized under steady state, studying their contribution to physiological and pathological processes has been hindered by the lack of specific targeting tools in vivo. Recent findings have shown that the dural sinus and its adjacent lymphatic vessels act as a neuroimmune interface. However, the cellular and functional heterogeneity of extrasinusoidal dural macrophages outside this immune hub is not fully understood. Therefore, we comprehensively characterized these cells using single-cell transcriptomics, fate mapping, confocal imaging, clonal analysis, and transgenic mouse lines. Extrasinusoidal dural macrophages were distinct from leptomeningeal and CNS parenchymal macrophages in terms of their origin, expansion kinetics, and transcriptional profiles. During autoimmune neuroinflammation, extrasinusoidal dural macrophages performed efferocytosis of apoptotic granulocytes. Our results highlight a previously unappreciated myeloid cell diversity and provide insights into the brain’s innate immune system.
AB - Although macrophages in the meningeal compartments of the central nervous system (CNS) have been comprehensively characterized under steady state, studying their contribution to physiological and pathological processes has been hindered by the lack of specific targeting tools in vivo. Recent findings have shown that the dural sinus and its adjacent lymphatic vessels act as a neuroimmune interface. However, the cellular and functional heterogeneity of extrasinusoidal dural macrophages outside this immune hub is not fully understood. Therefore, we comprehensively characterized these cells using single-cell transcriptomics, fate mapping, confocal imaging, clonal analysis, and transgenic mouse lines. Extrasinusoidal dural macrophages were distinct from leptomeningeal and CNS parenchymal macrophages in terms of their origin, expansion kinetics, and transcriptional profiles. During autoimmune neuroinflammation, extrasinusoidal dural macrophages performed efferocytosis of apoptotic granulocytes. Our results highlight a previously unappreciated myeloid cell diversity and provide insights into the brain’s innate immune system.
UR - http://www.scopus.com/inward/record.url?scp=85213498823&partnerID=8YFLogxK
U2 - 10.1126/sciimmunol.adh1129
DO - 10.1126/sciimmunol.adh1129
M3 - Article
C2 - 39705337
AN - SCOPUS:85213498823
SN - 2470-9468
VL - 9
JO - Science immunology
JF - Science immunology
IS - 102
M1 - eadh1129
ER -