<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xu H</submitter><funding>Strategic Priority Research Program of the Chinese Academy of Sciences</funding><funding>National Key Research &amp; Developmental Program of China</funding><funding>National Key R&amp;D Program of China</funding><funding>National Natural Science Foundation of China Program</funding><funding>National Key Research and Development Program of China</funding><funding>Strategic Collaborative Research Program of the Ferring Institute of Reproductive Medicine</funding><pagination>e13490</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10623959</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>56(11)</volume><pubmed_abstract>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&lt;sup>-&lt;/sup> PU.1&lt;sup>dim&lt;/sup> GATA-1&lt;sup>-&lt;/sup> (LPG) cell subset. In vivo competitive repopulation assays demonstrate that bone marrow cells gated by LPG exhibit haematopoietic reconstitution activity which is</pubmed_abstract><journal>Cell proliferation</journal><pubmed_title>Lin&lt;sup>-&lt;/sup> PU.1&lt;sup>dim&lt;/sup> GATA-1&lt;sup>-&lt;/sup> defines haematopoietic stem cells with long-term multilineage reconstitution activity.</pubmed_title><pmcid>PMC10623959</pmcid><funding_grant_id>33</funding_grant_id><funding_grant_id>XDA16040501</funding_grant_id><funding_grant_id>31720103907</funding_grant_id><funding_grant_id>2018YFA0108402</funding_grant_id><funding_grant_id>XDA16030302</funding_grant_id><funding_grant_id>31621004</funding_grant_id><funding_grant_id>2022YFA1103601</funding_grant_id><funding_grant_id>31570995</funding_grant_id><pubmed_authors>Tian J</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Cao W</pubmed_authors><pubmed_authors>Cao J</pubmed_authors><pubmed_authors>Tan S</pubmed_authors><pubmed_authors>Wang F</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Zhao T</pubmed_authors><pubmed_authors>Xu H</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lin&lt;sup>-&lt;/sup> PU.1&lt;sup>dim&lt;/sup> GATA-1&lt;sup>-&lt;/sup> defines haematopoietic stem cells with long-term multilineage reconstitution activity.</name><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&lt;sup>-&lt;/sup> PU.1&lt;sup>dim&lt;/sup> GATA-1&lt;sup>-&lt;/sup> (LPG) cell subset. In vivo competitive repopulation assays demonstrate that bone marrow cells gated by LPG exhibit haematopoietic reconstitution activity which is</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2025-04-21T23:50:48.372Z</modification><creation>2025-04-05T19:22:10.151Z</creation></dates><accession>S-EPMC10623959</accession><cross_references><pubmed>37147872</pubmed><doi>10.1111/cpr.13490</doi></cross_references></HashMap>