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Siret, C.; van Lessen, M.; Bavais, J.; Jeong, H. W.; Reddy Samawar, S. K.; Kapupara, K.; Wang, S.; Simic, M.; de Fabritus, L.; Tchoghandjian, A.; Fallet, M.; Huang, H.; Sarrazin, S.; Sieweke, M. H.; Stumm, R.; Sorokin, L.; Adams, R. H.; Schulte-Merker, S.; Kiefer, F.; van de Pavert, S. A.

Deciphering the heterogeneity of the Lyve1+ perivascular macrophages in the mouse brain

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  • Media type: E-Article
  • Title: Deciphering the heterogeneity of the Lyve1+ perivascular macrophages in the mouse brain
  • Contributor: Siret, C.; van Lessen, M.; Bavais, J.; Jeong, H. W.; Reddy Samawar, S. K.; Kapupara, K.; Wang, S.; Simic, M.; de Fabritus, L.; Tchoghandjian, A.; Fallet, M.; Huang, H.; Sarrazin, S.; Sieweke, M. H.; Stumm, R.; Sorokin, L.; Adams, R. H.; Schulte-Merker, S.; Kiefer, F.; van de Pavert, S. A.
  • imprint: Springer Science and Business Media LLC, 2022
  • Published in: Nature Communications
  • Language: English
  • DOI: 10.1038/s41467-022-35166-9
  • ISSN: 2041-1723
  • Origination:
  • Footnote:
  • Description: <jats:title>Abstract</jats:title><jats:p>Perivascular macrophages (pvMs) are associated with cerebral vasculature and mediate brain drainage and immune regulation. Here, using reporter mouse models, whole brain and section immunofluorescence, flow cytometry, and single cell RNA sequencing, besides the Lyve1<jats:sup>+</jats:sup>F4/80<jats:sup>+</jats:sup>CD206<jats:sup>+</jats:sup>CX3CR1<jats:sup>+</jats:sup> pvMs, we identify a CX3CR1<jats:sup>–</jats:sup> pvM population that shares phagocytic functions and location. Furthermore, the brain parenchyma vasculature mostly hosts Lyve1<jats:sup>+</jats:sup>MHCII<jats:sup>–</jats:sup> pvMs with low to intermediate CD45 expression. Using the double <jats:italic>Cx3cr1</jats:italic><jats:sup><jats:italic>GFP</jats:italic></jats:sup> x <jats:italic>Cx3cr1-Cre</jats:italic>;<jats:italic>Rosa</jats:italic><jats:sup><jats:italic>tdT</jats:italic></jats:sup> reporter mice for finer mapping of the lineages, we establish that CD45<jats:sup>low</jats:sup>CX3CR1<jats:sup>–</jats:sup> pvMs are derived from CX3CR1<jats:sup>+</jats:sup> precursors and require PU.1 during their ontogeny. In parallel, results from the <jats:italic>Cxcr4-CreErt2</jats:italic>;<jats:italic>Rosa26</jats:italic><jats:sup><jats:italic>tdT</jats:italic></jats:sup> lineage tracing model support a bone marrow-independent replenishment of all Lyve1<jats:sup>+</jats:sup> pvMs in the adult mouse brain. Lastly, flow cytometry and 3D immunofluorescence analysis uncover increased percentage of pvMs following photothrombotic induced stroke. Our results thus show that the parenchymal pvM population is more heterogenous than previously described, and includes a CD45<jats:sup>low</jats:sup> and CX3CR1<jats:sup>–</jats:sup> pvM population.</jats:p>
  • Access State: Open Access