A human pathophysiological 3D-bone marrow model reveals immune and stromal cell heterogeneity

The bone marrow niche is a complex microenvironment composed of stromal, endothelial, immune and hematopoietic cells. Dysregulated interactions within this niche can contribute to hematological malignancies and also occur in the context of solid cancer metastases. Here, we present a standardized three-dimensional human bone marrow (3D-BOM) model that recapitulates key features of the human niche. Indeed, we show that monocytes/macrophages from different sources acquire enhanced pro-inflammatory phenotype in 3D compared to 2D cultures. Hematopoietic progenitor cells are also influenced by this 3D niche while maintaining stemness characteristics over extended serial culture. Single-cell transcriptomics analysis highlighted human-like stromal and endothelial cells heterogeneity. In addition, we observed monocyte/macrophage and endothelial cell remodeling in the context of acute myeloid leukemia, suggesting dynamic interactions within the 3D-BOM. These findings highlight the potential of this model to investigate cellular dynamics underlying human bone marrow physiology and pathology.

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Publication Details

Journal
Communications Biology
Published
2026-01-03
DOI
https://doi.org/10.1038/s42003-025-09433-6
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00

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article

A human pathophysiological 3D-bone marrow model reveals immune and stromal cell heterogeneity

Sylvain Lefort, Kevin Geistlich, Véronique Maguer‐Satta, Mariette Giannini et al.
Communications Biology
Single-cell and spatial transcriptomics
article

A human pathophysiological 3D-bone marrow model reveals immune and stromal cell heterogeneity

Sylvain Lefort, Kevin Geistlich, Véronique Maguer‐Satta, Mariette Giannini, Giulia Campione, Julie Leca, Léa Torcq, Sophia Bounaud, Sandrine Jeanpierre, Maroua Bencheikh, Sylvain Donadelli
article en

Abstract

The bone marrow niche is a complex microenvironment composed of stromal, endothelial, immune and hematopoietic cells. Dysregulated interactions within this niche can contribute to hematological malignancies and also occur in the context of solid cancer metastases. Here, we present a standardized three-dimensional human bone marrow (3D-BOM) model that recapitulates key features of the human niche. Indeed, we show that monocytes/macrophages from different sources acquire enhanced pro-inflammatory phenotype in 3D compared to 2D cultures. Hematopoietic progenitor cells are also influenced by this 3D niche while maintaining stemness characteristics over extended serial culture. Single-cell transcriptomics analysis highlighted human-like stromal and endothelial cells heterogeneity. In addition, we observed monocyte/macrophage and endothelial cell remodeling in the context of acute myeloid leukemia, suggesting dynamic interactions within the 3D-BOM. These findings highlight the potential of this model to investigate cellular dynamics underlying human bone marrow physiology and pathology.

Communications BiologyVol. 9(1)
Université Claude Bernard Lyon 1 (FR), Centre National de la Recherche Scientifique (FR), Inserm (FR), Centre de Recherche en Cancérologie de Lyon (FR)
Institut National de la Santé et de la Recherche Médicale, Fondation de France, Centre National de la Recherche Scientifique, Institut National Du Cancer, Université Claude Bernard Lyon 1, Université de Lyon, Centre Léon Bérard
Good health and well-being
Openalex Percentile: Top 98%
Single-cell and spatial transcriptomics
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