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Lin(−) PU.1(dim)GATA‐1(−) defines haematopoietic stem cells with long‐term multilineage reconstitution activity
Despite extensive characterization of the state and function of haematopoietic stem cells (HSCs), the use of transcription factors to define the HSC population is still limited. We show here that the HSC population in mouse bone marrow can be defined by the distinct expression levels of Spi1 and Gat...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623959/ https://www.ncbi.nlm.nih.gov/pubmed/37147872 http://dx.doi.org/10.1111/cpr.13490 |
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author | Xu, Haoyu Tan, Shaojing Zhao, Yu Zhang, Lin Cao, Weiyun Li, Xing Tian, Jiayi Wang, Xiaojing Li, Xiaoyan Wang, Fengchao Cao, Jiani Zhao, Tongbiao |
author_facet | Xu, Haoyu Tan, Shaojing Zhao, Yu Zhang, Lin Cao, Weiyun Li, Xing Tian, Jiayi Wang, Xiaojing Li, Xiaoyan Wang, Fengchao Cao, Jiani Zhao, Tongbiao |
author_sort | Xu, Haoyu |
collection | PubMed |
description | Despite extensive characterization of the state and function of haematopoietic stem cells (HSCs), the use of transcription factors to define the HSC population is still limited. We show here that the HSC population in mouse bone marrow can be defined by the distinct expression levels of Spi1 and Gata1. By using a double fluorescence knock‐in mouse model, PGdKI, in which the expression levels of PU.1 and GATA‐1 are indicated by the expression of GFP and mCherry, respectively, we uncover that the HSCs with lymphoid and myeloid repopulating activity are specifically enriched in a Lin(−)PU.1(dim)GATA‐1(−) (LPG) cell subset. In vivo competitive repopulation assays demonstrate that bone marrow cells gated by LPG exhibit haematopoietic reconstitution activity which is comparable to that of classical Lin(−)Sca1(+)c‐kit(+) (LSK). The integrated analysis of single‐cell RNA sequence data from LPG and LSK‐gated cells reveals that a transcriptional network governed by core TFs contributes to regulation of HSC multipotency. These discoveries provide new clues for HSC characterization and functional study. |
format | Online Article Text |
id | pubmed-10623959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106239592023-11-04 Lin(−) PU.1(dim)GATA‐1(−) defines haematopoietic stem cells with long‐term multilineage reconstitution activity Xu, Haoyu Tan, Shaojing Zhao, Yu Zhang, Lin Cao, Weiyun Li, Xing Tian, Jiayi Wang, Xiaojing Li, Xiaoyan Wang, Fengchao Cao, Jiani Zhao, Tongbiao Cell Prolif Original Articles Despite extensive characterization of the state and function of haematopoietic stem cells (HSCs), the use of transcription factors to define the HSC population is still limited. We show here that the HSC population in mouse bone marrow can be defined by the distinct expression levels of Spi1 and Gata1. By using a double fluorescence knock‐in mouse model, PGdKI, in which the expression levels of PU.1 and GATA‐1 are indicated by the expression of GFP and mCherry, respectively, we uncover that the HSCs with lymphoid and myeloid repopulating activity are specifically enriched in a Lin(−)PU.1(dim)GATA‐1(−) (LPG) cell subset. In vivo competitive repopulation assays demonstrate that bone marrow cells gated by LPG exhibit haematopoietic reconstitution activity which is comparable to that of classical Lin(−)Sca1(+)c‐kit(+) (LSK). The integrated analysis of single‐cell RNA sequence data from LPG and LSK‐gated cells reveals that a transcriptional network governed by core TFs contributes to regulation of HSC multipotency. These discoveries provide new clues for HSC characterization and functional study. John Wiley and Sons Inc. 2023-05-05 /pmc/articles/PMC10623959/ /pubmed/37147872 http://dx.doi.org/10.1111/cpr.13490 Text en © 2023 The Authors. Cell Proliferation published by Beijing Institute for Stem Cell and Regenerative Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Xu, Haoyu Tan, Shaojing Zhao, Yu Zhang, Lin Cao, Weiyun Li, Xing Tian, Jiayi Wang, Xiaojing Li, Xiaoyan Wang, Fengchao Cao, Jiani Zhao, Tongbiao Lin(−) PU.1(dim)GATA‐1(−) defines haematopoietic stem cells with long‐term multilineage reconstitution activity |
title | Lin(−)
PU.1(dim)GATA‐1(−) defines haematopoietic stem cells with long‐term multilineage reconstitution activity |
title_full | Lin(−)
PU.1(dim)GATA‐1(−) defines haematopoietic stem cells with long‐term multilineage reconstitution activity |
title_fullStr | Lin(−)
PU.1(dim)GATA‐1(−) defines haematopoietic stem cells with long‐term multilineage reconstitution activity |
title_full_unstemmed | Lin(−)
PU.1(dim)GATA‐1(−) defines haematopoietic stem cells with long‐term multilineage reconstitution activity |
title_short | Lin(−)
PU.1(dim)GATA‐1(−) defines haematopoietic stem cells with long‐term multilineage reconstitution activity |
title_sort | lin(−)
pu.1(dim)gata‐1(−) defines haematopoietic stem cells with long‐term multilineage reconstitution activity |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623959/ https://www.ncbi.nlm.nih.gov/pubmed/37147872 http://dx.doi.org/10.1111/cpr.13490 |
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