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Exosomes derived from bone marrow mesenchymal stem cells facilitate repair of radiation-Induced skin injury by attenuating inflammation and apoptosis
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  • Published: 02 February 2026

Exosomes derived from bone marrow mesenchymal stem cells facilitate repair of radiation-Induced skin injury by attenuating inflammation and apoptosis

  • Yuxin Wen1,
  • Yiwei Song2,
  • Shichao Pan3,
  • Na Zhang4 &
  • …
  • Xu Tong4 

Scientific Reports , Article number:  (2026) Cite this article

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Cell biology
  • Molecular biology
  • Stem cells

Abstract

Radiation-induced skin injury (RISI) refers to injury to the skin resulting from exposure to ionizing radiation, for which current treatment options are limited. Exosomes derived from bone marrow mesenchymal stem cells (BMSCs-Exos) have demonstrated significant potential in tissue repair. This study evaluated the healing efficacy of BMSCs‑Exos in a rat model of RISI. BMSCs-Exos were isolated and delivered via subcutaneous injection into the RISI. Our findings revealed that BMSCs-Exos reduced the wound area and lowered the radiation injury score, thereby indicating their capacity to facilitate RISI healing. Histological analysis revealed that BMSCs-Exos enhanced epidermal repair and collagen deposition. Immunological assays revealed significantly higher CD31 and α‑SMA expression of the BMSCs‑Exos treatment group (EXO) than that of the irradiation group (IR), suggesting that BMSCs-Exos promoted angiogenesis. In the EXO group, there was also a downregulation of CD86, Inducible Nitric Oxide Synthase (INOS), Tumor Necrosis Factor-α (TNF-α) and Interleukin-1β (IL-1β) expression, coupled with an upregulation of Macrophage Mannose Receptor 1 (CD206), Arginase-1 (Arg-1), and Interleukin-10 (IL-10) expression, indicating that BMSCs-Exos can induce macrophage polarization towards the M2 phenotype and suppress inflammation. Additionally, BMSCs-Exos decreased the number of TUNEL-positive cells. Western blot analysis of apoptosis-related proteins showed that BMSCs-Exos increased the Bcl-2 expression and reduced Bax expression and promoted phosphorylation of the Akt signaling pathway, which implied suppression of cellular apoptosis. In summary, our findings demonstrate that BMSCs-Exos promote RISI repair by regulating the inflammatory microenvironment, and inhibiting cell apoptosis.

Data availability

The data used to support the findings of this study are available from the corresponding author upon request.

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Acknowledgements

The authors would like to thank Xu Tong for their valuable contributions to the study design and manuscript revisions. We also appreciate the Qiqihar Medical University for offering the experimental animals. Special thanks to all animals involved in the study.

Funding

This research was supported by the Joint Fund Cultivation Project of Heilongjiang Provincial Natural Science Foundation (PL2024H261), the Qiqihar Medical University Graduate Innovation Fund (QYYCX2023-12), and the Construction Project of Dominant Characteristic Disciplines of Qiqihar Medical University (QYZDXK-025, Oncology).

Author information

Authors and Affiliations

  1. College of Medical Technology, Qiqihar Medical University, Qiqihar, 161006, China

    Yuxin Wen

  2. The Third Clinical Medical College, Qiqihar Medical University, Qiqihar, 161006, China

    Yiwei Song

  3. Department of Radiology, Affiliated Hospital of Jining Medical University, Jining, 272000, China

    Shichao Pan

  4. Department of Radiation Oncology, The Third Affiliated Hospital of Qiqihar Medical University, Qiqihar, 161000, China

    Na Zhang & Xu Tong

Authors
  1. Yuxin Wen
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  2. Yiwei Song
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Contributions

Yuxin Wen and Xu Tong conceptualized the study; Shichao Pan and Na Zhang developed the methodology; Yuxin Wen and Yiwei Song performed the experiments and collected the data; Yuxin Wen analyzed the data and drafted the manuscript; Xu Tong and Shichao Pan reviewed and edited the manuscript. All authors reviewed and approved the final version of the paper.

Corresponding author

Correspondence to Xu Tong.

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Competing interests

The authors declare no competing interests.

Ethics approval and consent to participate

All experimental procedures and animal experiments were approved by the Animal Ethics Committee of Qiqihar Medical University, with approval number QMU-AECC-2024-7.

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Cite this article

Wen, Y., Song, Y., Pan, S. et al. Exosomes derived from bone marrow mesenchymal stem cells facilitate repair of radiation-Induced skin injury by attenuating inflammation and apoptosis. Sci Rep (2026). https://doi.org/10.1038/s41598-026-38306-z

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  • Received: 03 September 2025

  • Accepted: 29 January 2026

  • Published: 02 February 2026

  • DOI: https://doi.org/10.1038/s41598-026-38306-z

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Keywords

  • Radiation-induced skin injury
  • Exosomes
  • Bone marrow mesenchymal stem cells
  • Macrophage polarization
  • Inflammation
  • Apoptosis
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