Inflammation perturbs hematopoiesis by remodeling specific compartments of the bone marrow niche

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 stromal cells to abandon their normal stromal functions and instead adopt an inflammatory phenotype associated with overproduction of chemokines that modulate local monocyte dynamics in the surrounding microenvironment. Our results provide a comprehensive method for molecular and functional stromal characterization and highlight the importance of altered stomal cell activity in regulating hematopoietic responses to inflammatory challenges.

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Publication Details

Journal
Blood
Published
2025-10-08
DOI
https://doi.org/10.1182/blood.2025029513
Citations
2
Primary Topic
Immune cells in cancer
Type
article
Field-Weighted Citation Impact
1.59

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Inflammation perturbs hematopoiesis by remodeling specific compartments of the bone marrow niche

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Inflammation perturbs hematopoiesis by remodeling specific compartments of the bone marrow niche

Peter Shyu, Emmanuelle Passegué, Berthold Göttgens, Lei Ding, Evgenia Verovskaya, Brian Heubel, Melissa Proven, Fernando J. Calero‐Nieto, Ruiyuan Zhang, James W. Swann, Xiaonan Wang, X. Edward Guo, Hiroyuki Hirakawa
article en
2 citations

Abstract

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 stromal cells to abandon their normal stromal functions and instead adopt an inflammatory phenotype associated with overproduction of chemokines that modulate local monocyte dynamics in the surrounding microenvironment. Our results provide a comprehensive method for molecular and functional stromal characterization and highlight the importance of altered stomal cell activity in regulating hematopoietic responses to inflammatory challenges.

BloodVol. 147(7)
Shanghai Jiao Tong University (CN), Wellcome/MRC Cambridge Stem Cell Institute (GB), University of Cambridge (GB), CHI Health Creighton University Medical Center - Bergan Mercy (US), Stem Cell Institute (PA), Thermo Fisher Scientific (United States) (US), Broad Center (US), Columbia University (US)
Damon Runyon Cancer Research Foundation, New York State Stem Cell Science, York University, Cancer Research UK, National Institutes of Health, Irving Medical Center, Columbia University, National Cancer Institute
Openalex Percentile: Top 14%
Immune cells in cancer
1.59
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