Department of Medicine, Division of Allergy and Immunology, National Jewish Health, 1400 Jackson Street, Denver, CO 80206, USA.
Immunity. 2013 Jul 25;39(1):97-110. doi: 10.1016/j.immuni.2013.06.012. Epub 2013 Jul 18.
It remains unclear whether basophils and mast cells are derived from a common progenitor. Furthermore, how basophil versus mast cell fate is specified has not been investigated. Here, we have identified a population of granulocyte-macrophage progenitors (GMPs) that were highly enriched in the capacity to differentiate into basophils and mast cells while retaining a limited capacity to differentiate into myeloid cells. We have designated these progenitor cells "pre-basophil and mast cell progenitors" (pre-BMPs). STAT5 signaling was required for the differentiation of pre-BMPs into both basophils and mast cells and was critical for inducing two downstream molecules: C/EBPα and MITF. We have identified C/EBPα as the critical basophil transcription factor for specifying basophil cell fate and MITF as the crucial transcription factor for specifying mast cell fate. C/EBPα and MITF silenced each other's transcription in a directly antagonistic fashion. Our study reveals how basophil and mast cell fate is specified.
目前尚不清楚嗜碱性粒细胞和肥大细胞是否来自共同的祖细胞。此外,嗜碱性粒细胞与肥大细胞命运的特化方式尚未得到研究。在这里,我们鉴定了一群粒细胞-巨噬细胞祖细胞(GMP),这些细胞高度富集于分化为嗜碱性粒细胞和肥大细胞的能力,同时保留了分化为髓样细胞的有限能力。我们将这些祖细胞命名为“前嗜碱性粒细胞和肥大细胞祖细胞”(pre-BMP)。STAT5 信号对于 pre-BMP 分化为嗜碱性粒细胞和肥大细胞是必需的,并且对于诱导两个下游分子:C/EBPα 和 MITF 至关重要。我们已经确定 C/EBPα 是决定嗜碱性粒细胞命运的关键转录因子,而 MITF 是决定肥大细胞命运的关键转录因子。C/EBPα 和 MITF 以直接拮抗的方式相互抑制对方的转录。我们的研究揭示了嗜碱性粒细胞和肥大细胞命运的特化方式。