Extracellular Vesicles Define Discrete Nano‐Based Niches Within the Human Haematopoietic System

Stem cell niches are complex multi-signalling networks comprised of molecular cues and physical interactions, orchestrated by niche-resident cells and the extracellular factors they produce. The bone niche specifically houses haematopoietic stem cells (HSCs), a critical cell type responsible for producing all blood and immune cells throughout life. Currently, how niches facilitate an ideal environment with simultaneously coordinating both intrinsic and extrinsic cellular signals is unknown. Studies presented here identify the existence of unique extracellular vesicle (EV)-defined niches within the haematopoietic system of human individuals. Bridging studies using proteomic signatures, nanoparticle characterization at single-vesicle resolution and machine learning-based techniques reveal that EVs can be grouped by blood, bone marrow and trabeculae within a human individual. Stem cell assays demonstrate that these niche-defined EVs impart functional effects on stem cells/progenitors based on location within the haematopoietic system. Finally, using single-cell transcriptomic analyses, results identify for the first time how niche-sourced EVs differentially affect the most primitive human HSCs and progenitors. This study highlights the significance of nanoparticles on human immunity and blood production and provides evidence for a new role for EVs, namely the demarcation of distinct nano-niches within biological systems.

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Publication Details

Journal
Journal of Extracellular Vesicles
Published
2025-11-27
DOI
https://doi.org/10.1002/jev2.70181
Citations
1
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
0.81
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article

Extracellular Vesicles Define Discrete Nano‐Based Niches Within the Human Haematopoietic System

Simon Vilms Pedersen, Kathrin Tyryshkin, Sarah A. Dick, Jamie Beaulieu et al.
1 citations
Journal of Extracellular Vesicles
Extracellular vesicles in disease
0.81
article

Extracellular Vesicles Define Discrete Nano‐Based Niches Within the Human Haematopoietic System

Simon Vilms Pedersen, Kathrin Tyryshkin, Sarah A. Dick, Jamie Beaulieu, Isabelle Grenier‐Pleau, Lynne‐Marie Postovit, Stephen M. Mann, Michael Vermeulen, Jasleen Kaur, Mykhaylo Slobodyanyuk, S. Holmes, David J. H. F. Knapp, Jelle Penders, Éric Bonneil, Michael J. Rauh, Stephanie Zhi-Juan Xie, Sheela A. Abraham, Christine Hall, Amy J. M. McNaughton, Camille A. de Villiers, Murtaza S. Nagree, Jüri Reimand, Andrew W. Craig, C A Wells, John F. Rudan, Pierre Thibault, Edmond Y. W. Chan
article en
1 citations

Abstract

Stem cell niches are complex multi-signalling networks comprised of molecular cues and physical interactions, orchestrated by niche-resident cells and the extracellular factors they produce. The bone niche specifically houses haematopoietic stem cells (HSCs), a critical cell type responsible for producing all blood and immune cells throughout life. Currently, how niches facilitate an ideal environment with simultaneously coordinating both intrinsic and extrinsic cellular signals is unknown. Studies presented here identify the existence of unique extracellular vesicle (EV)-defined niches within the haematopoietic system of human individuals. Bridging studies using proteomic signatures, nanoparticle characterization at single-vesicle resolution and machine learning-based techniques reveal that EVs can be grouped by blood, bone marrow and trabeculae within a human individual. Stem cell assays demonstrate that these niche-defined EVs impart functional effects on stem cells/progenitors based on location within the haematopoietic system. Finally, using single-cell transcriptomic analyses, results identify for the first time how niche-sourced EVs differentially affect the most primitive human HSCs and progenitors. This study highlights the significance of nanoparticles on human immunity and blood production and provides evidence for a new role for EVs, namely the demarcation of distinct nano-niches within biological systems.

Journal of Extracellular VesiclesVol. 14(12)
Ontario Institute for Cancer Research (CA), University Health Network (CA), University of Southern Denmark (DK), University of Toronto (CA), Queen's University (CA), Princess Margaret Cancer Centre (CA), University of Oxford (GB), Institute for Research in Immunology and Cancer (CA), CRUK/MRC Oxford Institute for Radiation Oncology (GB), Sunny BioDiscovery (United States) (US), Imperial College London (GB)
Openalex Percentile: Top 21%
Extracellular vesicles in disease
0.81
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