{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Dawson A"],"funding":["Cancer Research UK","Kay Kendall Leukaemia Fund","Kay Kendall Leukaemia Fund (KKLF)"],"pagination":["1090"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10844594"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["15(1)"],"pubmed_abstract":["Macrophages are fundamental cells of the innate immune system that support normal haematopoiesis and play roles in both anti-cancer immunity and tumour progression. Here we use a chimeric mouse model of chronic myeloid leukaemia (CML) and human bone marrow (BM) derived macrophages to study the impact of the dysregulated BM microenvironment on bystander macrophages. Utilising single-cell RNA sequencing (scRNA-seq) of Philadelphia chromosome (Ph) negative macrophages we reveal unique subpopulations of immature macrophages residing in the CML BM microenvironment. CML exposed macrophages separate from their normal counterparts by reduced expression of the surface marker CD36, which significantly reduces clearance of apoptotic cells. We uncover aberrant production of CML-secreted factors, inclu"],"journal":["Nature communications"],"pubmed_title":["Leukaemia exposure alters the transcriptional profile and function of BCR::ABL1 negative macrophages in the bone marrow niche."],"pmcid":["PMC10844594"],"funding_grant_id":["KKL698","A29800","A29754"],"pubmed_authors":["Agarwal P","Tiong OS","Helgason GV","Bittencourt-Silvestre J","Bhatia R","Kerekes Z","Blanco GR","van Loon I","Dawson A","Kirschner K","Zerbst D","Krishnan V","Hsieh YC","Scott MT","Himonas E","Copland M","Vetrie D","Hopcroft LEM","McCluskey L","Baquero P","Zarou MM","Ianniciello A","Dunn K","Wheadon H","Zanivan S","Prasad B","Coffelt SB","Almasoudi H"],"additional_accession":[]},"is_claimable":false,"name":"Leukaemia exposure alters the transcriptional profile and function of BCR::ABL1 negative macrophages in the bone marrow niche.","description":"Macrophages are fundamental cells of the innate immune system that support normal haematopoiesis and play roles in both anti-cancer immunity and tumour progression. Here we use a chimeric mouse model of chronic myeloid leukaemia (CML) and human bone marrow (BM) derived macrophages to study the impact of the dysregulated BM microenvironment on bystander macrophages. Utilising single-cell RNA sequencing (scRNA-seq) of Philadelphia chromosome (Ph) negative macrophages we reveal unique subpopulations of immature macrophages residing in the CML BM microenvironment. CML exposed macrophages separate from their normal counterparts by reduced expression of the surface marker CD36, which significantly reduces clearance of apoptotic cells. We uncover aberrant production of CML-secreted factors, inclu","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Feb","modification":"2025-04-22T05:39:09.87Z","creation":"2025-04-05T21:24:59.086Z"},"accession":"S-EPMC10844594","cross_references":{"pubmed":["38316788"],"doi":["10.1038/s41467-024-45471-0"]}}