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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
*Corresponding author for this work
Scholary Output:
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Article
Research
Peer-review

Open access

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.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Research
Peer-review

Original language

English (US)

Article number

10055

Journal (Volume, Issue Number)

Scientific reports (Volume 5)

Publication milestones

  • Published - 06/19/2015

Publication status

Published - 06/19/2015

ISSN

2045-2322

Publication IDs

  • Scopus: 84934927579
  • PubMed: 26091486

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Funding Details

We would like to thank D. Yoakum, A. Blatchley, and the LJI microscopy and flow cytometry cores for excellent technical assistance. This work was supported by funding from NIH R01 HL118765 (to C.C.H.), NIH P01 HL055798 (to C.C.H.) and the American Heart Association 13POST16990029 (to R.T.).
FundersFunding numbers
NIH
R01 HL118765, P01 HL055798
NCRR
S10RR027366
AHA
13POST16990029