| Literature DB >> 27135602 |
Tobias Goldmann1, Peter Wieghofer1,2, Marta Joana Costa Jordão1,2, Fabiola Prutek1, Nora Hagemeyer1, Kathrin Frenzel1,2, Lukas Amann1,2, Ori Staszewski1, Katrin Kierdorf1, Martin Krueger3, Giuseppe Locatelli4, Hannah Hochgerner5, Robert Zeiser6,7, Slava Epelman8, Frederic Geissmann9, Josef Priller10, Fabio M V Rossi11, Ingo Bechmann3, Martin Kerschensteiner4,12, Sten Linnarsson5, Steffen Jung13, Marco Prinz1,7.
Abstract
Perivascular, subdural meningeal and choroid plexus macrophages are non-parenchymal macrophages that mediate immune responses at brain boundaries. Although the origin of parenchymal microglia has recently been elucidated, much less is known about the precursors, the underlying transcriptional program and the dynamics of the other macrophages in the central nervous system (CNS). It was assumed that they have a high turnover from blood-borne monocytes. However, using parabiosis and fate-mapping approaches in mice, we found that CNS macrophages arose from hematopoietic precursors during embryonic development and established stable populations, with the notable exception of choroid plexus macrophages, which had dual origins and a shorter life span. The generation of CNS macrophages relied on the transcription factor PU.1, whereas the MYB, BATF3 and NR4A1 transcription factors were not required.Entities:
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Year: 2016 PMID: 27135602 PMCID: PMC4968048 DOI: 10.1038/ni.3423
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606