IRF8 deficiency induces the transcriptional, functional, and epigenetic reprogramming of cDC1 into the cDC2 lineage

Telma Lança, Jonas Ungerbäck, Clément Da Silva, Thorsten Joeris, Fatemeh Ahmadi, Julien Vandamme, Marcus Svensson-Frej, Allan McI Mowat, Knut Kotarsky, Mikael Sigvardsson, William W Agace

Research output: Contribution to journalArticlepeer-review

1 Citation (SciVal)

Abstract

Conventional dendritic cells (cDCs) consist of two major functionally and phenotypically distinct subsets, cDC1 and cDC2, whose development is dependent on distinct sets of transcription factors. Interferon regulatory factor 8 (IRF8) is required at multiple stages of cDC1 development, but its role in committed cDC1 remains unclear. Here, we used Xcr1-cre to delete Irf8 in committed cDC1 and demonstrate that Irf8 is required for maintaining the identity of cDC1. In the absence of Irf8, committed cDC1 acquired the transcriptional, functional, and chromatin accessibility properties of cDC2. This conversion was independent of Irf4 and was associated with the decreased accessibility of putative IRF8, Batf3, and composite AP-1-IRF (AICE)-binding elements, together with increased accessibility of cDC2-associated transcription-factor-binding elements. Thus, IRF8 expression by committed cDC1 is required for preventing their conversion into cDC2-like cells.

Original languageEnglish
Pages (from-to)1431-1447.e11
JournalImmunity
Volume55
Issue number8
DOIs
Publication statusPublished - 2022 Aug 9

Subject classification (UKÄ)

  • Immunology in the medical area

Keywords

  • ATAC-sequencing
  • cDC1
  • cDC2
  • dendritic cell identity
  • IRF
  • IRF4
  • IRF8
  • transcription factor
  • transcriptional regulation
  • transcriptional reprogramming

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