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Single cell analyses identify a highly regenerative and homogenous human CD34+ hematopoietic stem cell population

The heterogeneous nature of human CD34(+) hematopoietic stem cells (HSCs) has hampered our understanding of the cellular and molecular trajectories that HSCs navigate during lineage commitment. Using various platforms including single cell RNA-sequencing and extensive xenotransplantation, we have un...

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Autores principales: Anjos-Afonso, Fernando, Buettner, Florian, Mian, Syed A., Rhys, Hefin, Perez-Lloret, Jimena, Garcia-Albornoz, Manuel, Rastogi, Namrata, Ariza-McNaughton, Linda, Bonnet, Dominique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018830/
https://www.ncbi.nlm.nih.gov/pubmed/35440586
http://dx.doi.org/10.1038/s41467-022-29675-w
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author Anjos-Afonso, Fernando
Buettner, Florian
Mian, Syed A.
Rhys, Hefin
Perez-Lloret, Jimena
Garcia-Albornoz, Manuel
Rastogi, Namrata
Ariza-McNaughton, Linda
Bonnet, Dominique
author_facet Anjos-Afonso, Fernando
Buettner, Florian
Mian, Syed A.
Rhys, Hefin
Perez-Lloret, Jimena
Garcia-Albornoz, Manuel
Rastogi, Namrata
Ariza-McNaughton, Linda
Bonnet, Dominique
author_sort Anjos-Afonso, Fernando
collection PubMed
description The heterogeneous nature of human CD34(+) hematopoietic stem cells (HSCs) has hampered our understanding of the cellular and molecular trajectories that HSCs navigate during lineage commitment. Using various platforms including single cell RNA-sequencing and extensive xenotransplantation, we have uncovered an uncharacterized human CD34(+) HSC population. These CD34(+)EPCR(+)(CD38/CD45RA)(−) (simply as EPCR(+)) HSCs have a high repopulating and self-renewal abilities, reaching a stem cell frequency of ~1 in 3 cells, the highest described to date. Their unique transcriptomic wiring in which many gene modules associated with differentiated cell lineages confers their multilineage lineage output both in vivo and in vitro. At the single cell level, EPCR(+) HSCs are the most transcriptomically and functionally homogenous human HSC population defined to date and can also be easily identified in post-natal tissues. Therefore, this EPCR(+) population not only offers a high human HSC resolution but also a well-structured human hematopoietic hierarchical organization at the most primitive level.
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spelling pubmed-90188302022-04-28 Single cell analyses identify a highly regenerative and homogenous human CD34+ hematopoietic stem cell population Anjos-Afonso, Fernando Buettner, Florian Mian, Syed A. Rhys, Hefin Perez-Lloret, Jimena Garcia-Albornoz, Manuel Rastogi, Namrata Ariza-McNaughton, Linda Bonnet, Dominique Nat Commun Article The heterogeneous nature of human CD34(+) hematopoietic stem cells (HSCs) has hampered our understanding of the cellular and molecular trajectories that HSCs navigate during lineage commitment. Using various platforms including single cell RNA-sequencing and extensive xenotransplantation, we have uncovered an uncharacterized human CD34(+) HSC population. These CD34(+)EPCR(+)(CD38/CD45RA)(−) (simply as EPCR(+)) HSCs have a high repopulating and self-renewal abilities, reaching a stem cell frequency of ~1 in 3 cells, the highest described to date. Their unique transcriptomic wiring in which many gene modules associated with differentiated cell lineages confers their multilineage lineage output both in vivo and in vitro. At the single cell level, EPCR(+) HSCs are the most transcriptomically and functionally homogenous human HSC population defined to date and can also be easily identified in post-natal tissues. Therefore, this EPCR(+) population not only offers a high human HSC resolution but also a well-structured human hematopoietic hierarchical organization at the most primitive level. Nature Publishing Group UK 2022-04-19 /pmc/articles/PMC9018830/ /pubmed/35440586 http://dx.doi.org/10.1038/s41467-022-29675-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Anjos-Afonso, Fernando
Buettner, Florian
Mian, Syed A.
Rhys, Hefin
Perez-Lloret, Jimena
Garcia-Albornoz, Manuel
Rastogi, Namrata
Ariza-McNaughton, Linda
Bonnet, Dominique
Single cell analyses identify a highly regenerative and homogenous human CD34+ hematopoietic stem cell population
title Single cell analyses identify a highly regenerative and homogenous human CD34+ hematopoietic stem cell population
title_full Single cell analyses identify a highly regenerative and homogenous human CD34+ hematopoietic stem cell population
title_fullStr Single cell analyses identify a highly regenerative and homogenous human CD34+ hematopoietic stem cell population
title_full_unstemmed Single cell analyses identify a highly regenerative and homogenous human CD34+ hematopoietic stem cell population
title_short Single cell analyses identify a highly regenerative and homogenous human CD34+ hematopoietic stem cell population
title_sort single cell analyses identify a highly regenerative and homogenous human cd34+ hematopoietic stem cell population
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018830/
https://www.ncbi.nlm.nih.gov/pubmed/35440586
http://dx.doi.org/10.1038/s41467-022-29675-w
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