The Enhancing Effects and Underlying Mechanism of Ionizing Radiation on Adipogenic Differentiation of Mesenchymal Stem Cells via Regulating Oxidative Stress Pathway.
10.19746/j.cnki.issn.1009-2137.2025.01.037
- Author:
Fu-Hao YU
1
;
Bo-Feng YIN
2
;
Pei-Lin LI
2
;
Xiao-Tong LI
2
;
Jia-Yi TIAN
3
;
Run-Xiang XU
1
;
Jie TANG
2
;
Xiao-Yu ZHANG
2
;
Wen-Jing ZHANG
2
;
Heng ZHU
2
;
Li DING
1
Author Information
1. Graduate School of Air Force Medical University, Xi'an 710032, Shaanxi Province, China.
2. Institute of Radiation Medicine, Military Medical College, Beijing 100850, China.
3. Department of Hematology, Air Force Medical University, Air Force Medical Center, PLA, Beijing 100142, China.
- Publication Type:Journal Article
- Keywords:
ionizing radiation;
bone marrow microenvironment;
mesenchymal stem cells;
adipogenic differentiation;
oxidative stress
- MeSH:
Mesenchymal Stem Cells/cytology*;
Oxidative Stress/radiation effects*;
Animals;
Adipogenesis/radiation effects*;
Mice;
Radiation, Ionizing;
Cell Differentiation/radiation effects*;
Humans;
NF-E2-Related Factor 2/metabolism*;
PPAR gamma;
Cells, Cultured
- From:
Journal of Experimental Hematology
2025;33(1):246-254
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the effects and underlying mechanism of ionizing radiation on the adipogenic of mesenchymal stem cells (MSCs).
METHODS:Mouse MSCs were cultured in vitro and treated with 2 Gy and 6 Gy radiation with 60Co, and the radiation dose rate was 0.98 Gy/min. Bulk RNA-seq was performed on control and irradiated MSCs. The changes of adipogenic differentiation and oxidative stress pathways of MSC were revealed by bioinformatics analysis. Oil Red O staining was used to detect the adipogenic differentiation ability of MSCs in vitro, and real-time fluorescence quantitative PCR (qPCR) was used to detect the expression differences of key regulatory factors Cebpa, Lpl and Pparg after radiation treatment. At the same time, qPCR and Western blot were used to detect the effect of inhibition of Nrf2, a key factor of antioxidant stress pathway, on the expression of key regulatory factors of adipogenesis. Moreover, the species conservation of the irradiation response of human bone marrow MSCs and mouse MSC was determined by qPCR.
RESULTS:Bulk RNA-seq suggested that ionizing radiation promotes adipogenic differentiation of MSCs and up-regulation of oxidative stress-related genes and pathways. The results of Oil Red O staining and qPCR showed that ionizing radiation promoted the adipogenesis of MSCs, with high expression of Cebpa, Lpl and Pparg, as well as oxidative stress-related gene Nrf2. Nrf2 pathway inhibitors could further enhance the adipogenesis of MSCs in bone marrow after radiation. Notably, the similar regulation of oxidative pathways and enhanced adipogenesis post irradiation were observed in human bone marrow MSCs. In addition, irradiation exposure led to up-regulated mRNA expression of interleukin-6 and down-regulated mRNA expression of colony stimulating factor 2 in human bone marrow MSCs.
CONCLUSION:Ionizing radiation promotes adipogenesis of MSCs in mice, and oxidative stress pathway participates in this effect, blocking Nrf2 further promotes the adipogenesis of MSCs. Additionally, irradiation activates oxidative pathways and promotes adipogenic differentiation of human bone marrow MSCs.
