Department of Immunology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Department of Microbiology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Nat Commun. 2014 Sep 19;5:4978. doi: 10.1038/ncomms5978.
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.
髓系祖细胞在向单核吞噬细胞谱系分化时会失去生成中性粒细胞的潜能。导致这种谱系限制的机制尚不清楚。我们在这里报告,IRF8 的蛋白表达,一种树突状细胞 (DC) 和单核细胞发育所必需的转录因子,在单核细胞-树突状细胞祖细胞 (MDP) 阶段急剧增加,并在普通单核细胞祖细胞 (cMoP) 中保持高水平。Irf8(-/-)MDP 和 cMoP 积累但未能有效地生成其下游群体,而是在体内产生中性粒细胞。IRF8 与转录因子 C/EBPα 发生物理相互作用,并阻止其在 MDP 和 cMoP 中与染色质结合,从而阻止 C/EBPα 刺激转录和中性粒细胞分化的能力。在 Irf8(-/-)造血祖细胞中部分抑制 C/EBP 活性可减轻体内中性粒细胞过度生成。因此,IRF8 不仅赋予单核吞噬细胞祖细胞单核细胞和 DC 分化潜能,而且还阻止这些祖细胞分化为中性粒细胞。