Iwasaki Hiromi, Mizuno Shin-ichi, Arinobu Yojiro, Ozawa Hidetoshi, Mori Yasuo, Shigematsu Hirokazu, Takatsu Kiyoshi, Tenen Daniel G, Akashi Koichi
Center for Cellular and Molecular Medicine, Kyushu University Hospital, Fukuoka, Japan.
Genes Dev. 2006 Nov 1;20(21):3010-21. doi: 10.1101/gad.1493506.
The mechanism of lineage specification in multipotent stem cells has not been fully understood. We recently isolated progenitors with the eosinophil, basophil, or mast cell lineage potential, all of which originate from granulocyte/monocyte progenitors (GMPs). By using these prospectively purified progenitors, we show here that the expression timing of GATA-2 and CCAAT enhancer-binding protein alpha (C/EBPalpha) can differentially control their lineage commitment. The expression of GATA-2 instructed C/EBPalpha-expressing GMPs to commit exclusively into the eosinophil lineage, while it induced basophil and/or mast cell lineage commitment if C/EBPalpha was suppressed at the GMP stage. Furthermore, simply by switching the order of C/EBPalpha and GATA-2 transduction, even lymphoid-committed progenitors recaptured these developmental processes to be reprogrammed into each of these lineages. We propose that the order of expression of key transcription factors is critical for their interplay to selectively drive lineage specification programs, by which stem cells could generate multiple lineage cells in a hierarchical manner.
多能干细胞中谱系特化的机制尚未完全明确。我们最近分离出了具有嗜酸性粒细胞、嗜碱性粒细胞或肥大细胞谱系潜能的祖细胞,它们均起源于粒细胞/单核细胞祖细胞(GMPs)。通过使用这些经前瞻性纯化的祖细胞,我们在此表明,GATA-2和CCAAT增强子结合蛋白α(C/EBPα)的表达时机可差异性地控制它们的谱系定向。GATA-2的表达促使表达C/EBPα的GMPs专门定向分化为嗜酸性粒细胞谱系,而如果在GMP阶段C/EBPα受到抑制,它则诱导嗜碱性粒细胞和/或肥大细胞谱系的定向分化。此外,仅仅通过改变C/EBPα和GATA-2转导的顺序,即使是已定向分化为淋巴细胞的祖细胞也能重新经历这些发育过程,从而被重新编程为这些谱系中的每一种细胞。我们提出,关键转录因子的表达顺序对于它们相互作用以选择性驱动谱系特化程序至关重要,通过这一过程干细胞能够以分级方式产生多种谱系细胞。