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September 18, 2025International Journal of Molecular Sciences3 citationsOpen Access

Interactions of Hematopoietic and Associated Mesenchymal Stem Cell Populations in the Bone Marrow Microenvironment, In Vivo and In Vitro Model

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DBDarina BačenkováMTMarianna TrebuňováEDErik Dosedla

Key Points

  • The interactions between hematopoietic stem cells and mesenchymal stem cells are crucial for maintaining stemness in the bone marrow.
  • In vitro simulations of the bone marrow microenvironment using biomaterials can advance our understanding of hematopoiesis.
  • The study identifies specific phenotypes characterizing MSC subclusters that interact within the bone marrow.
  • Understanding the complex microenvironment is vital for both physiological and pathological research in hematopoiesis.

Abstract

Multipotent hematopoietic stem cells (HSC) reside in specialized niches of the bone marrow (BM). The maintenance of their stemness requires a precisely regulated bone marrow microenvironment (BMM), supported by mesenchymal stem cells (MSCs), stromal reticular cells, and endothelial and nerve cells located within the vascular and endosteal niches. The heterogeneity of the niche environment is caused by the diversity of cell populations from HSCs to more mature hematopoietic cell types and MSCs, which collectively influence the complex intercellular interactions involved in hematopoiesis. MSC subclusters in BM are characterized by the phenotypes of CXC-chemokine ligand 12, leptin receptor, neuron-glial antigen 2, and Nestin+ cells. The article presents a detailed characterization of individual stem cell types in the BM, their reciprocal interaction, and the possibility of in vitro simulation of the bone marrow niche as a dynamic structure. Development of a suitable simulation of the BMM is essential for advancing research into both physiological and pathological processes of hematopoiesis. The main goal is to simulate 3D cell culture using biomaterials that mimic the BM niche in the form of hydrogels and scaffolds, in combination with extracellular matrix components.

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Cite This Study

Bačenková et al. (2025) studied this question.

synapsesocial.com/papers/68d462ca31b076d99fa62049https://doi.org/10.3390/ijms26189036
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Mesenchymal stem cells1991 · 6,525 citations
  2. 2Short-Term Hematopoietic Stem Cells (ST-HSC) Have Full Long-Term Capacity with Sustained but Reduced Potential Compared with LT-HSC.2009 · 2 citations
  3. 3Handbook of the Hemopoietic Microenvironment1989 · 34 citations
  4. 4Adhesion and homing of blood-borne cells in bone marrow microvessels1999 · 124 citations
  5. 5Osteoclast-Mediated Bone Resorption Is Stimulated During Short-Term Administration of Granulocyte Colony-Stimulating Factor But Is Not Responsible for Hematopoietic Progenitor Cell Mobilization1998 · 136 citations