<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Swann JW</submitter><funding>NIDDK NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>Wellcome Trust</funding><pagination>739-754</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7618457</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>147(7)</volume><pubmed_abstract>&lt;h4>Abstract&lt;/h4>Hematopoietic stem and progenitor cells are regulated by interactions with stromal cells in the bone marrow (BM) cavity, which can be segregated into 2 spatially defined central marrow (CM) and endosteal (Endo) compartments. However, the importance of this spatial compartmentalization for BM responses to complex conditions such as inflammation remains largely unknown. Here, we extensively validate a combination of single-cell RNA sequencing profiling and matching flow cytometry isolation that reproducibly identifies 7 key CM and Endo populations and accurately surveys both niche locations. We demonstrate that inflammatory perturbations exert specific effects on different cellular compartments, with type I interferon responses causing leptin receptor-expressing mesenchymal </pubmed_abstract><journal>Blood</journal><pubmed_title>Inflammation perturbs hematopoiesis by remodeling specific compartments of the bone marrow niche.</pubmed_title><pmcid>PMC7618457</pmcid><funding_grant_id>206328</funding_grant_id><funding_grant_id>R01 CA184014</funding_grant_id><funding_grant_id>TL1 DK136048</funding_grant_id><funding_grant_id>R35 HL135763</funding_grant_id><funding_grant_id>P30 CA013696</funding_grant_id><pubmed_authors>Gottgens B</pubmed_authors><pubmed_authors>Guo XE</pubmed_authors><pubmed_authors>Zhang R</pubmed_authors><pubmed_authors>Ding L</pubmed_authors><pubmed_authors>Shyu PT</pubmed_authors><pubmed_authors>Heubel BP</pubmed_authors><pubmed_authors>Verovskaya EV</pubmed_authors><pubmed_authors>Hirakawa H</pubmed_authors><pubmed_authors>Passegue E</pubmed_authors><pubmed_authors>Calero-Nieto FJ</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Proven MA</pubmed_authors><pubmed_authors>Swann JW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Inflammation perturbs hematopoiesis by remodeling specific compartments of the bone marrow niche.</name><description>&lt;h4>Abstract&lt;/h4>Hematopoietic stem and progenitor cells are regulated by interactions with stromal cells in the bone marrow (BM) cavity, which can be segregated into 2 spatially defined central marrow (CM) and endosteal (Endo) compartments. However, the importance of this spatial compartmentalization for BM responses to complex conditions such as inflammation remains largely unknown. Here, we extensively validate a combination of single-cell RNA sequencing profiling and matching flow cytometry isolation that reproducibly identifies 7 key CM and Endo populations and accurately surveys both niche locations. We demonstrate that inflammatory perturbations exert specific effects on different cellular compartments, with type I interferon responses causing leptin receptor-expressing mesenchymal </description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-16T09:42:31.056Z</modification><creation>2026-07-09T10:46:57.175Z</creation></dates><accession>S-EPMC7618457</accession><cross_references><pubmed>41060335</pubmed><doi>10.1182/blood.2025029513</doi></cross_references></HashMap>