TY - JOUR
T1 - Transcriptional Heterogeneity and Lineage Commitment in Myeloid Progenitors
AU - Paul, Franziska
AU - Arkin, Ya'Ara
AU - Giladi, Amir
AU - Jaitin, Diego Adhemar
AU - Kenigsberg, Ephraim
AU - Keren-Shaul, Hadas
AU - Winter, Deborah
AU - Lara-Astiaso, David
AU - Gury, Meital
AU - Weiner, Assaf
AU - David, Eyal
AU - Cohen, Nadav
AU - Lauridsen, Felicia Kathrine Bratt
AU - Haas, Simon
AU - Schlitzer, Andreas
AU - Mildner, Alexander
AU - Ginhoux, Florent
AU - Jung, Steffen
AU - Trumpp, Andreas
AU - Porse, Bo Torben
AU - Tanay, Amos
AU - Amit, Ido
N1 - Publisher Copyright:
© 2015 Elsevier Inc. All rights reserved.
PY - 2015/12/17
Y1 - 2015/12/17
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84950290139&partnerID=8YFLogxK
U2 - 10.1016/j.cell.2015.11.013
DO - 10.1016/j.cell.2015.11.013
M3 - Article
C2 - 26627738
AN - SCOPUS:84950290139
SN - 0092-8674
VL - 163
SP - 1663
EP - 1677
JO - Cell
JF - Cell
IS - 7
ER -