| Literature DB >> 25236377 |
Daisuke Kurotaki1, Michio Yamamoto1, Akira Nishiyama1, Kazuhiro Uno1, Tatsuma Ban1, Motohide Ichino1, Haruka Sasaki1, Satoko Matsunaga2, Masahiro Yoshinari1, Akihide Ryo2, Masatoshi Nakazawa3, Keiko Ozato4, Tomohiko Tamura1.
Abstract
Myeloid progenitors lose their potential to generate neutrophils when they adopt the mononuclear phagocyte lineage. The mechanism underlying this lineage restriction remains unknown. We here report that the protein expression of IRF8, an essential transcription factor for the development of dendritic cells (DCs) and monocytes, sharply increases at the monocyte-DC progenitor (MDP) stage and remains high in common monocyte progenitors (cMoPs). Irf8(-/-) MDPs and cMoPs accumulate but fail to efficiently generate their downstream populations, instead giving rise to neutrophils in vivo. IRF8 physically interacts with the transcription factor C/EBPα and prevents its binding to chromatin in MDPs and cMoPs, blocking the ability of C/EBPα to stimulate transcription and neutrophil differentiation. A partial inhibition of C/EBP activity in Irf8(-/-) haematopoietic progenitors alleviates the neutrophil overproduction in vivo. Thus, IRF8 not only bestows monocyte and DC differentiation potential upon mononuclear phagocyte progenitors but also restrains these progenitors from differentiating into neutrophils.Entities:
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Year: 2014 PMID: 25236377 DOI: 10.1038/ncomms5978
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919