Author
Listed:
- Philipp S. Hoppe
(Department of Biosystems Science and Engineering
Research Unit Stem Cell Dynamics, Helmholtz Zentrum München)
- Michael Schwarzfischer
(Institute of Computational Biology, Helmholtz Zentrum München)
- Dirk Loeffler
(Department of Biosystems Science and Engineering
Research Unit Stem Cell Dynamics, Helmholtz Zentrum München)
- Konstantinos D. Kokkaliaris
(Department of Biosystems Science and Engineering
Research Unit Stem Cell Dynamics, Helmholtz Zentrum München)
- Oliver Hilsenbeck
(Department of Biosystems Science and Engineering
Research Unit Stem Cell Dynamics, Helmholtz Zentrum München
Institute of Computational Biology, Helmholtz Zentrum München)
- Nadine Moritz
(Research Unit Stem Cell Dynamics, Helmholtz Zentrum München)
- Max Endele
(Department of Biosystems Science and Engineering
Research Unit Stem Cell Dynamics, Helmholtz Zentrum München)
- Adam Filipczyk
(Research Unit Stem Cell Dynamics, Helmholtz Zentrum München)
- Adriana Gambardella
(MRC Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford)
- Nouraiz Ahmed
(Department of Biosystems Science and Engineering)
- Martin Etzrodt
(Department of Biosystems Science and Engineering)
- Daniel L. Coutu
(Department of Biosystems Science and Engineering)
- Michael A. Rieger
(Research Unit Stem Cell Dynamics, Helmholtz Zentrum München)
- Carsten Marr
(Institute of Computational Biology, Helmholtz Zentrum München)
- Michael K. Strasser
(Institute of Computational Biology, Helmholtz Zentrum München)
- Bernhard Schauberger
(Research Unit Stem Cell Dynamics, Helmholtz Zentrum München)
- Ingo Burtscher
(Institute of Diabetes and Regeneration Research, Institute of Stem Cell Research, Helmholtz Zentrum München)
- Olga Ermakova
(Istituto di Biologia Cellulare e Neurobiologia, CNR)
- Antje Bürger
(Institute of Developmental Genetics, Helmholtz Zentrum München)
- Heiko Lickert
(Institute of Diabetes and Regeneration Research, Institute of Stem Cell Research, Helmholtz Zentrum München
Beta Cell Biology, Medical Faculty, Technical University Munich (TUM))
- Claus Nerlov
(MRC Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, University of Oxford
EMBL Mouse Biology Unit)
- Fabian J. Theis
(Institute of Computational Biology, Helmholtz Zentrum München
Technical University Munich)
- Timm Schroeder
(Department of Biosystems Science and Engineering
Research Unit Stem Cell Dynamics, Helmholtz Zentrum München)
Abstract
Live imaging and single-cell analyses are used to show that decision-making by differentiating haematopoietic stem cells between the megakaryocytic–erythroid and granulocytic–monocytic lineages is not initiated by stochastic switching between the lineage-specific transcription factors PU.1 and GATA1, which challenges the previous model of early myeloid lineage choice.
Suggested Citation
Philipp S. Hoppe & Michael Schwarzfischer & Dirk Loeffler & Konstantinos D. Kokkaliaris & Oliver Hilsenbeck & Nadine Moritz & Max Endele & Adam Filipczyk & Adriana Gambardella & Nouraiz Ahmed & Martin, 2016.
"Early myeloid lineage choice is not initiated by random PU.1 to GATA1 protein ratios,"
Nature, Nature, vol. 535(7611), pages 299-302, July.
Handle:
RePEc:nat:nature:v:535:y:2016:i:7611:d:10.1038_nature18320
DOI: 10.1038/nature18320
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