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Assessment of the Immunomodulatory Properties of Human Mesenchymal Stem Cells MSCs
Published on: December 24, 2015
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Low-dose radiation modulates human mesenchymal stem cell proliferation through regulating CDK and Rb
Lei Yang1, Ziling Liu1, Chen Chen1
1Cancer Center, The First Hospital of Jilin UniversityChangchun 130021, China.
American Journal of Translational Research
|May 5, 2017
Summary
Low-dose radiation (LDR) significantly boosts human bone marrow mesenchymal stem cell (BMSC) proliferation and enhances their ability to modulate T-cell activity. This suggests LDR could be a valuable tool for expanding BMSCs for clinical cell therapy.
Area of Science:
- Stem cell biology
- Radiation biology
- Immunology
Background:
- Low-dose radiation (LDR) is known to stimulate cell proliferation.
- The specific effects of LDR on human bone marrow mesenchymal stem cells (BMSCs) require further investigation.
Purpose of the Study:
- To investigate the impact of LDR on human BMSC proliferation.
- To elucidate the underlying mechanisms of LDR-induced BMSC proliferation.
Main Methods:
- Human BMSCs were isolated and cultured with or without LDR (75 mGy).
- Cell proliferation was assessed using MTT assays.
- Cytokine production and cell cycle-associated proteins were analyzed via ELISA and immunoblotting, respectively.
Main Results:
- LDR significantly stimulated human BMSC proliferation and increased the S-phase proportion.
- LDR enhanced the production of stem cell factor (SCF), granulocyte-macrophage colony-stimulating factor (GM-CSF), and interleukin-11 (IL-11).
- LDR augmented the modulatory effect of BMSCs on T-cell proliferation, with cell cycle proteins like Rb, CDK1, and CDC25B mediating these effects.
Conclusions:
- LDR effectively stimulates human BMSC proliferation and enhances their immunomodulatory functions.
- LDR presents a potential physical stimulant for large-scale BMSC expansion for clinical applications in cell therapy.
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