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Updated: Oct 7, 2025

Bioengineering of Humanized Bone Marrow Microenvironments in Mouse and Their Visualization by Live Imaging
Published on: August 1, 2017
The bone marrow niche components are adversely affected in sepsis
Fan Yin1, Han Qian1, Caiwen Duan2
1Department of Pediatric Intensive Care Unit, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, 1678 Dongfang Road, Shanghai, China.
Sepsis causes early and significant bone marrow (BM) damage, altering BM niche components like vascular structures and regulatory T cells. These findings highlight adaptive changes within the BM niche during sepsis.
Area of Science:
- Immunology
- Hematology
- Pathology
Background:
- Sepsis-induced multiple organ dysfunction is a leading cause of mortality.
- The impact of sepsis on the bone marrow (BM) niche and its cellular components remains understudied.
Purpose of the Study:
- To investigate the early pathological changes in the mouse bone marrow (BM) niche during sepsis.
- To analyze alterations in vascular structures, mesenchymal stem cells, and regulatory T cells within the BM niche.
Main Methods:
- Established mouse models of sepsis using lipopolysaccharide (LPS) injection and cecal ligation and puncture (CLP).
- Observed and analyzed major BM niche components, including vascular structures, mesenchymal stem cells, and regulatory T cells (Tregs).
Main Results:
- Bone marrow (BM) pathological changes were observed earlier and were more pronounced than in other organs.
- Significant alterations in BM niche cell components were detected, including transient increases in vascular endothelial cells with remodeling.
- A sustained decrease in regulatory T cells (Tregs) was observed over time.
Conclusions:
- Sepsis induces early and prominent pathological changes in the bone marrow (BM).
- The BM niche undergoes significant adaptive cellular changes in response to sepsis.
- Alterations in vascular endothelial cells and regulatory T cells are key features of the BM response to sepsis.
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