Neural Regeneration Research ›› 2023, Vol. 18 ›› Issue (9): 1861-1868.doi: 10.4103/1673-5374.367838

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Mesenchymal stem cells, extracellular vesicles, and transcranial magnetic stimulation for ferroptosis after spinal cord injury

Qi-Feng Song, Qian Cui, Ya-Shi Wang, Li-Xin Zhang*   

  1. Department of Rehabilitation, Shengjing Hospital of China Medical University, Shenyang, Liaoning Province, China
  • Online:2023-09-15 Published:2023-03-03
  • Contact: Li-Xin Zhang, PhD, uzhanglx@aliyun.com.
  • Supported by:
    This work was supported by a grant from funded by the National Natural Science Foundation of China (Youth Program), No. 81101462; Natural Science Foundation of Liaoning Province, Nos. 201602875 and 2019-KF-01-06; Liaoning Provincial Public Welfare Science Foundation Project, No. 2016003001; University of China Medical University Discipline Development Project, No. 112-3110119071 (all to LXZ).

Abstract: Spinal cord injury is characterized by different aetiologies, complex pathogenesis, and diverse pathological changes. Current treatments are not ideal, and prognosis is generally poor. After spinal cord injury, neurons die due to various forms of cell death. Among them, ferroptosis causes dysfunction after spinal cord injury, and no existing traditional treatments have been indicated to block its occurrence. Meanwhile, emerging therapies using mesenchymal stem cells, extracellular vesicles, and transcranial magnetic stimulation therapy are promising for reversing spinal cord neuronal ferroptosis after spinal cord injury. However, no definitive studies have demonstrated the effectiveness of these approaches. This review summarizes the existing research on the mechanisms of ferroptosis; ferroptosis after spinal cord injury; treatment of spinal cord injury with mesenchymal stem cells, extracellular vesicles, and transcranial magnetic stimulation; and treatment of ferroptosis using mesenchymal stem cells, extracellular vesicles, and transcranial magnetic stimulation. Inhibiting ferroptosis can promote the reversal of neurological dysfunction after spinal cord injury. In addition, mesenchymal stem cells, extracellular vesicles, and transcranial magnetic stimulation can reverse adverse outcomes of spinal cord injury and regulate ferroptosis-related factors. Thus, it can be inferred that mesenchymal stem cells, extracellular vesicles, and transcranial magnetic stimulation have the potential to inhibit ferroptosis after spinal cord injury. This review serves as a reference for future research to confirm these conclusions.

Key words: exosomes, extracellular vesicles, ferroptosis, iron overload, lipid peroxidation, mesenchymal stem cells, miRNAs, spinal cord injury, stem cells, transcranial magnetic stimulation