The transcription factor NR4A1 is essential for the development of a novel macrophage subset in the thymus

Robert Tacke, Ingo Hilgendorf, Hannah Garner, Claire Waterborg, Kiwon Park, Heba Nowyhed, Richard N. Hanna, Runpei Wu, Filip K. Swirski, Frederic Geissmann, Catherine C. Hedrick

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

Abstract

Tissue macrophages function to maintain homeostasis and regulate immune responses. While tissue macrophages derive from one of a small number of progenitor programs, the transcriptional requirements for site-specific macrophage subset development are more complex. We have identified a new tissue macrophage subset in the thymus and have discovered that its development is dependent on transcription factor NR4A1. Functionally, we find that NR4A1-dependent macrophages are critically important for clearance of apoptotic thymocytes. These macrophages are largely reduced or absent in mice lacking NR4A1, and Nr4a1-deficient mice have impaired thymocyte engulfment and clearance. Thus, NR4A1 functions as a master transcription factor for the development of this novel thymus-specific macrophage subset.

Original languageEnglish (US)
Article number10055
JournalScientific reports
Volume5
DOIs
StatePublished - Jun 19 2015
Externally publishedYes

ASJC Scopus subject areas

  • General

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