生物
祖细胞
细胞生物学
启动(农业)
髓样
干细胞
细胞分化
造血
重编程
祖细胞
转录因子
骨髓
遗传学
细胞
免疫学
基因
植物
发芽
作者
Franziska Paul,Ya’ara Arkin,Amir Giladi,Diego Adhemar Jaitin,Ephraim Kenigsberg,Hadas Keren‐Shaul,Deborah R. Winter,David Lara‐Astiaso,Meital Gury,Assaf Weiner,Eyal David,Nadav Cohen,Felicia Kathrine Bratt Lauridsen,Simon Haas,Andreas Schlitzer,Alexander Mildner,Florent Ginhoux,Steffen Jung,Andreas Trumpp,Bo Porse
出处
期刊:Cell
[Cell Press]
日期:2015-11-25
卷期号:163 (7): 1663-1677
被引量:1154
标识
DOI:10.1016/j.cell.2015.11.013
摘要
Within the bone marrow, stem cells differentiate and give rise to diverse blood cell types and functions. Currently, hematopoietic progenitors are defined using surface markers combined with functional assays that are not directly linked with in vivo differentiation potential or gene regulatory mechanisms. Here, we comprehensively map myeloid progenitor subpopulations by transcriptional sorting of single cells from the bone marrow. We describe multiple progenitor subgroups, showing unexpected transcriptional priming toward seven differentiation fates but no progenitors with a mixed state. Transcriptional differentiation is correlated with combinations of known and previously undefined transcription factors, suggesting that the process is tightly regulated. Histone maps and knockout assays are consistent with early transcriptional priming, while traditional transplantation experiments suggest that in vivo priming may still allow for plasticity given strong perturbations. These data establish a reference model and general framework for studying hematopoiesis at single-cell resolution.
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