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Human haematopoietic stem cell lineage commitment is a continuous process

Blood formation is believed to occur through step-wise progression of haematopoietic stem cells (HSCs) following a tree-like hierarchy of oligo-, bi- and unipotent progenitors. However, this model is based on the analysis of predefined flow-sorted cell populations. Here we integrated flow cytometric...

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Autores principales: Velten, Lars, Haas, Simon F., Raffel, Simon, Blaszkiewicz, Sandra, Islam, Saiful, Hennig, Bianca P., Hirche, Christoph, Lutz, Christoph, Buss, Eike C., Nowak, Daniel, Boch, Tobias, Hofmann, Wolf-Karsten, Ho, Anthony D., Huber, Wolfgang, Trumpp, Andreas, Essers, Marieke A.G., Steinmetz, Lars M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496982/
https://www.ncbi.nlm.nih.gov/pubmed/28319093
http://dx.doi.org/10.1038/ncb3493
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author Velten, Lars
Haas, Simon F.
Raffel, Simon
Blaszkiewicz, Sandra
Islam, Saiful
Hennig, Bianca P.
Hirche, Christoph
Lutz, Christoph
Buss, Eike C.
Nowak, Daniel
Boch, Tobias
Hofmann, Wolf-Karsten
Ho, Anthony D.
Huber, Wolfgang
Trumpp, Andreas
Essers, Marieke A.G.
Steinmetz, Lars M.
author_facet Velten, Lars
Haas, Simon F.
Raffel, Simon
Blaszkiewicz, Sandra
Islam, Saiful
Hennig, Bianca P.
Hirche, Christoph
Lutz, Christoph
Buss, Eike C.
Nowak, Daniel
Boch, Tobias
Hofmann, Wolf-Karsten
Ho, Anthony D.
Huber, Wolfgang
Trumpp, Andreas
Essers, Marieke A.G.
Steinmetz, Lars M.
author_sort Velten, Lars
collection PubMed
description Blood formation is believed to occur through step-wise progression of haematopoietic stem cells (HSCs) following a tree-like hierarchy of oligo-, bi- and unipotent progenitors. However, this model is based on the analysis of predefined flow-sorted cell populations. Here we integrated flow cytometric, transcriptomic and functional data at single-cell resolution to quantitatively map early differentiation of human HSCs towards lineage commitment. During homeostasis, individual HSCs gradually acquire lineage biases along multiple directions without passing through discrete hierarchically organized progenitor populations. Instead, unilineage-restricted cells emerge directly from a “Continuum of LOw primed UnDifferentiated hematopoietic stem- and progenitor cells” (CLOUD-HSPCs). Distinct gene expression modules operate in a combinatorial manner to control stemness, early lineage priming and the subsequent progression into all major branches of haematopoiesis. These data reveal a continuous landscape of human steady state haematopoiesis downstream of HSCs and provide a basis for the understanding of hematopoietic malignancies.
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spelling pubmed-54969822017-09-20 Human haematopoietic stem cell lineage commitment is a continuous process Velten, Lars Haas, Simon F. Raffel, Simon Blaszkiewicz, Sandra Islam, Saiful Hennig, Bianca P. Hirche, Christoph Lutz, Christoph Buss, Eike C. Nowak, Daniel Boch, Tobias Hofmann, Wolf-Karsten Ho, Anthony D. Huber, Wolfgang Trumpp, Andreas Essers, Marieke A.G. Steinmetz, Lars M. Nat Cell Biol Article Blood formation is believed to occur through step-wise progression of haematopoietic stem cells (HSCs) following a tree-like hierarchy of oligo-, bi- and unipotent progenitors. However, this model is based on the analysis of predefined flow-sorted cell populations. Here we integrated flow cytometric, transcriptomic and functional data at single-cell resolution to quantitatively map early differentiation of human HSCs towards lineage commitment. During homeostasis, individual HSCs gradually acquire lineage biases along multiple directions without passing through discrete hierarchically organized progenitor populations. Instead, unilineage-restricted cells emerge directly from a “Continuum of LOw primed UnDifferentiated hematopoietic stem- and progenitor cells” (CLOUD-HSPCs). Distinct gene expression modules operate in a combinatorial manner to control stemness, early lineage priming and the subsequent progression into all major branches of haematopoiesis. These data reveal a continuous landscape of human steady state haematopoiesis downstream of HSCs and provide a basis for the understanding of hematopoietic malignancies. 2017-03-20 2017-04 /pmc/articles/PMC5496982/ /pubmed/28319093 http://dx.doi.org/10.1038/ncb3493 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Velten, Lars
Haas, Simon F.
Raffel, Simon
Blaszkiewicz, Sandra
Islam, Saiful
Hennig, Bianca P.
Hirche, Christoph
Lutz, Christoph
Buss, Eike C.
Nowak, Daniel
Boch, Tobias
Hofmann, Wolf-Karsten
Ho, Anthony D.
Huber, Wolfgang
Trumpp, Andreas
Essers, Marieke A.G.
Steinmetz, Lars M.
Human haematopoietic stem cell lineage commitment is a continuous process
title Human haematopoietic stem cell lineage commitment is a continuous process
title_full Human haematopoietic stem cell lineage commitment is a continuous process
title_fullStr Human haematopoietic stem cell lineage commitment is a continuous process
title_full_unstemmed Human haematopoietic stem cell lineage commitment is a continuous process
title_short Human haematopoietic stem cell lineage commitment is a continuous process
title_sort human haematopoietic stem cell lineage commitment is a continuous process
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496982/
https://www.ncbi.nlm.nih.gov/pubmed/28319093
http://dx.doi.org/10.1038/ncb3493
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