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Combined single-cell and spatial transcriptomics reveal the molecular, cellular and spatial bone marrow niche organization.


ABSTRACT: The bone marrow constitutes the primary site for life-long blood production and skeletal regeneration. However, its cellular and spatial organization remains controversial. Here, we combine single-cell and spatially resolved transcriptomics to systematically map the molecular, cellular and spatial composition of distinct bone marrow niches. This allowed us to transcriptionally profile all major bone-marrow-resident cell types, determine their localization and clarify sources of pro-haematopoietic factors. Our data demonstrate that Cxcl12-abundant-reticular (CAR) cell subsets (Adipo-CAR and Osteo-CAR) differentially localize to sinusoidal and arteriolar surfaces, act locally as 'professional cytokine-secreting cells' and thereby establish peri-vascular micro-niches. Importantly, the three-dimensional bone-marrow organization can be accurately inferred from single-cell transcriptome data using the RNA-Magnet algorithm described here. Together, our study reveals the cellular and spatial organization of bone marrow niches and offers a systematic approach to dissect the complex organization of whole organs.

SUBMITTER: Baccin C 

PROVIDER: S-EPMC7610809 | biostudies-literature | 2020 Jan

REPOSITORIES: biostudies-literature

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Combined single-cell and spatial transcriptomics reveal the molecular, cellular and spatial bone marrow niche organization.

Baccin Chiara C   Al-Sabah Jude J   Velten Lars L   Helbling Patrick M PM   Grünschläger Florian F   Hernández-Malmierca Pablo P   Nombela-Arrieta César C   Steinmetz Lars M LM   Trumpp Andreas A   Haas Simon S  

Nature cell biology 20191223 1


The bone marrow constitutes the primary site for life-long blood production and skeletal regeneration. However, its cellular and spatial organization remains controversial. Here, we combine single-cell and spatially resolved transcriptomics to systematically map the molecular, cellular and spatial composition of distinct bone marrow niches. This allowed us to transcriptionally profile all major bone-marrow-resident cell types, determine their localization and clarify sources of pro-haematopoieti  ...[more]

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