| Literature DB >> 26627738 |
Franziska Paul1, Ya'ara Arkin2, Amir Giladi1, Diego Adhemar Jaitin1, Ephraim Kenigsberg2, Hadas Keren-Shaul1, Deborah Winter1, David Lara-Astiaso1, Meital Gury1, Assaf Weiner1, Eyal David1, Nadav Cohen2, Felicia Kathrine Bratt Lauridsen3, Simon Haas4, Andreas Schlitzer5, Alexander Mildner1, Florent Ginhoux6, Steffen Jung1, Andreas Trumpp4, Bo Torben Porse3, Amos Tanay7, Ido Amit8.
Abstract
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.Mesh:
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Year: 2015 PMID: 26627738 DOI: 10.1016/j.cell.2015.11.013
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582