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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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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. |
format | Online Article Text |
id | pubmed-5496982 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
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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