<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang C</submitter><funding>Yinfeng Plan of Tangdu hospital</funding><funding>National Natural Science Foundation of China</funding><pagination>155</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12607142</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Osteoporosis (OP) could lead to the alteration of bone marrow microenvironment and non-homeostasis of hematopoiesis, which could increase the incidence of hematologic malignancies. However, whether myeloid-biased hematopoiesis occurred and contributed to the leukemogenesis under the condition of OP remains unclear.&lt;h4>Results&lt;/h4>This study successfully induced a mouse model for OP by hindlimb unloading, which shows increased myeloid cells and decreased B cells in the peripheral blood (PB). Furthermore, our study demonstrates that the myeloid-biased subset of HSPCs (hematopoietic stem and progenitor cells) with reduced differentiation and apoptosis, including multipotent progenitor 3 (MPP3) and granulocyte-monocyte progenitors (GMPs), were expanded in the OP mice. The ex</pubmed_abstract><journal>Cell &amp; bioscience</journal><pubmed_title>Single-cell transcriptome analysis profiles the enlarged subsets of myeloid-biased HSPCs with preleukemic characters in disuse osteoporosis mice.</pubmed_title><pmcid>PMC12607142</pmcid><funding_grant_id>82200171</funding_grant_id><funding_grant_id>2021YFJH009</funding_grant_id><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Lou D</pubmed_authors><pubmed_authors>Liang H</pubmed_authors><pubmed_authors>Gu F</pubmed_authors><pubmed_authors>Wan Z</pubmed_authors><pubmed_authors>Ji Y</pubmed_authors><pubmed_authors>Gao X</pubmed_authors><pubmed_authors>Qin W</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-cell transcriptome analysis profiles the enlarged subsets of myeloid-biased HSPCs with preleukemic characters in disuse osteoporosis mice.</name><description>&lt;h4>Background&lt;/h4>Osteoporosis (OP) could lead to the alteration of bone marrow microenvironment and non-homeostasis of hematopoiesis, which could increase the incidence of hematologic malignancies. However, whether myeloid-biased hematopoiesis occurred and contributed to the leukemogenesis under the condition of OP remains unclear.&lt;h4>Results&lt;/h4>This study successfully induced a mouse model for OP by hindlimb unloading, which shows increased myeloid cells and decreased B cells in the peripheral blood (PB). Furthermore, our study demonstrates that the myeloid-biased subset of HSPCs (hematopoietic stem and progenitor cells) with reduced differentiation and apoptosis, including multipotent progenitor 3 (MPP3) and granulocyte-monocyte progenitors (GMPs), were expanded in the OP mice. The ex</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-10T03:14:32.067Z</modification><creation>2026-06-10T03:07:57.523Z</creation></dates><accession>S-EPMC12607142</accession><cross_references><pubmed>41225641</pubmed><doi>10.1186/s13578-025-01499-3</doi></cross_references></HashMap>