| Literature DB >> 32259484 |
Sebastian G Utz1, Peter See2, Wiebke Mildenberger1, Morgane Sonia Thion3, Aymeric Silvin4, Mirjam Lutz1, Florian Ingelfinger1, Nirmala Arul Rayan5, Iva Lelios1, Anne Buttgereit1, Kenichi Asano6, Shyam Prabhakar5, Sonia Garel3, Burkhard Becher1, Florent Ginhoux7, Melanie Greter8.
Abstract
Central nervous system (CNS) macrophages comprise microglia and border-associated macrophages (BAMs) residing in the meninges, the choroid plexus, and the perivascular spaces. Most CNS macrophages emerge during development, with the exception of choroid plexus and dural macrophages, which are replaced by monocytes in adulthood. Whether microglia and BAMs share a developmental program or arise from separate lineages remains unknown. Here, we identified two phenotypically, transcriptionally, and locally distinct brain macrophages throughout development, giving rise to either microglia or BAMs. Two macrophage populations were already present in the yolk sac suggesting an early segregation. Fate-mapping models revealed that BAMs mostly derived from early erythro-myeloid progenitors in the yolk sac. The development of microglia was dependent on TGF-β, whereas the genesis of BAMs occurred independently of this cytokine. Collectively, our data show that developing parenchymal and non-parenchymal brain macrophages are separate entities in terms of ontogeny, gene signature, and requirement for TGF-β.Entities:
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Year: 2020 PMID: 32259484 DOI: 10.1016/j.cell.2020.03.021
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582