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ORIGINAL RESEARCH article

Front. Bioeng. Biotechnol.

Sec. Tissue Engineering and Regenerative Medicine

Volume 13 - 2025 | doi: 10.3389/fbioe.2025.1554292

This article is part of the Research Topic Application of Tissue Engineering in Bone, Joints, Ligaments Injuries and Cartilage Regeneration View all 3 articles

MRI Monitoring of USPIO-Labeled BMSCs Combined with Alginate Scaffold for Cartilage Defect Repair

Provisionally accepted
Shanyu Lu Shanyu Lu 1,2Zhenyu Liu Zhenyu Liu 1,2Meiling Qi Meiling Qi 1,2Haocheng Zhen Haocheng Zhen 3Jing Luo Jing Luo 4Yingchao Wang Yingchao Wang 1,2Le Chang Le Chang 1,2Xiaolong Bai Xiaolong Bai 1,2Yingguang Jiao Yingguang Jiao 1,2Xinyao Chen Xinyao Chen 1,2Junping Zhen Junping Zhen 2*
  • 1 College of Medical Imaging, Shanxi Medical University, Taiyuan, Shanxi Province, China
  • 2 Department of Imaging, Second Hospital of Shanxi Medical University, Taiyuan, China
  • 3 Shandong First Medical University, Tai'an, Shandong, China
  • 4 Shanxi Key Laboratory for Immunomicroecology, Second Hospital of Shanxi Medical University, Taiyuan, China

The final, formatted version of the article will be published soon.

    Objective: This study aimed to evaluate the effectiveness of bone marrow mesenchymal stem cells (BMSCs) combined with sodium alginate scaffolds in repairing knee cartilage defects in New Zealand rabbits. Additionally, it assessed the potential of functional magnetic resonance imaging (fMRI) for non-invasive monitoring of the dynamic repair process.Methods: Rabbits were randomly divided into four groups: Group A (control), Group B (sodium alginate scaffold), Group C (BMSCs-sodium alginate scaffold), and Group D (USPIO-labeled BMSCs-sodium alginate scaffold). A cartilage defect model was created, and the respective materials were implanted into the defect regions. T2 mapping MRI was performed at weeks 1, 2, and 4 post-surgery to evaluate the repair process, followed by histological analysis to confirm the outcomes.Results: BMSCs significantly promoted cartilage defect repair and accelerated the degradation of sodium alginate scaffolds. Macroscopic and histological evaluations revealed repair tissue formation in Groups C and D by week 1, with most defect regions filled with new cartilage by week 4. T2 mapping analysis showed a gradual decline in T2 values in Group B, a more pronounced decrease in Group C, and consistently lower T2 values in Group D compared to Group C, with a slow upward trend over time.Conclusion: This study demonstrated that BMSCs exhibit significant regenerative potential for cartilage defect repair. USPIO labeling enables non-invasive, dynamic monitoring of the repair process without adverse effects on cell viability or differentiation. These findings provide experimental evidence supporting the application of BMSCs combined with magnetic labeling technology in cartilage regeneration.

    Keywords: cartilage repair, T2 mapping MRI, USPIO, Bone marrow mesenchymal stem cells, non-invasive monitoring

    Received: 01 Jan 2025; Accepted: 03 Mar 2025.

    Copyright: © 2025 Lu, Liu, Qi, Zhen, Luo, Wang, Chang, Bai, Jiao, Chen and Zhen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Junping Zhen, Department of Imaging, Second Hospital of Shanxi Medical University, Taiyuan, China

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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