| Literature DB >> 28273455 |
Ari Itoh-Nakadai1, Mitsuyo Matsumoto2, Hiroki Kato3, Junichi Sasaki3, Yukihiro Uehara3, Yuki Sato3, Risa Ebina-Shibuya4, Mizuho Morooka3, Ryo Funayama5, Keiko Nakayama5, Kyoko Ochiai6, Akihiko Muto7, Kazuhiko Igarashi8.
Abstract
Hematopoietic stem cell and multipotent progenitor (MPP) commitment can be tuned in response to an infection so that their differentiation is biased toward myeloid cells. Here, we find that Bach2, which inhibits myeloid differentiation in common lymphoid progenitors, represses a cohort of myeloid genes and activates those linked to lymphoid function. Bach2 repressed both Cebpb and its target Csf1r, encoding C/EBPβ and macrophage colony-stimulating factor receptor (M-CSFr), respectively, whereas C/EBPβ repressed Bach2 and activated Csf1r. Bach2 and C/EBPβ further bound to overlapping regulatory regions at their myeloid target genes, suggesting the presence of a gene regulatory network (GRN) with mutual repression between these factors and a feedforward loop leading to myeloid gene regulation. Lipopolysaccharide reduced the expression of Bach2, resulting in enhanced myeloid differentiation. The Bach2-C/EBPβ GRN pathway thus tunes MPP commitment to myeloid and lymphoid lineages both under normal conditions and after infection.Entities:
Keywords: B cells; gene regulatory network; infection; inner myeloid; lineage commitment; multipotent progenitors; stem cells; super enhancers; transcription factors
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Year: 2017 PMID: 28273455 DOI: 10.1016/j.celrep.2017.02.029
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423