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  4. MiR-31 improves spinal cord injury in mice by promoting the migration of bone marrow mesenchymal stem cells

MiR-31 improves spinal cord injury in mice by promoting the migration of bone marrow mesenchymal stem cells

PLOS ONE, 2022 · DOI: https://doi.org/10.1371/journal.pone.0272499 · Published: September 6, 2022

Spinal Cord InjuryRegenerative MedicineGenetics

Simple Explanation

This study investigates the potential of miR-31, a small RNA molecule, to enhance the migration of bone marrow mesenchymal stem cells (BMSCs) towards spinal cord injuries in mice. Stem cell transplantation is a promising therapy for spinal cord injuries, but its effectiveness is limited by the poor migration of transplanted cells to the injury site. The researchers found that miR-31 promotes the proliferation and migration of BMSCs in vitro (in cell cultures). They also observed that miR-31 upregulates the expression of proteins called CXCR4 and MMP-2, which are known to play a role in cell migration. In vivo (in living mice) experiments confirmed that miR-31 enhances the migration of BMSCs to the injured spinal cord, reduces inflammation, and improves functional recovery. These findings suggest that miR-31 could be a valuable tool for improving stem cell-based therapies for spinal cord injuries.

Study Duration
Not specified
Participants
FVB mice (8–10 weeks, 18-25g)
Evidence Level
Not specified

Key Findings

  • 1
    MiR-31 promotes the proliferation of BMSCs in vitro, as demonstrated by CCK-8 and Cell-cycle assays.
  • 2
    MiR-31 enhances the migration of BMSCs in vitro, as evidenced by wound-healing and transwell assays.
  • 3
    In vivo experiments showed that miR-31agomir group showed enhanced cell-targeted migration ability (P<0.001), improved the function of damaged tissues (P<0.001), and upregulated CXCR4 and MMP-2 expression compared to the control group (P<0.001).

Research Summary

This study aimed to investigate the effects of miR-31 on the migration of bone marrow mesenchymal stem cells (BMSCs) and the regulation of MMP-2 and CXCR4 expression in vitro and in vivo. In vitro experiments showed that cells in the miR-31agomir group exhibited enhanced cell proliferation (P<0.05, P<0.001) and migration (P<0.001) and upregulated protein expression levels of CXCR4 (P<0.01) and MMP-2 (P<0.001) compared with cells in the control group. Our experiment demonstrated that miR-31 could promote the migration of BMSCs and miR-31 could repair and improve the function of damaged tissues in SCI.

Practical Implications

Enhanced Stem Cell Therapy

MiR-31 could be used to pretreat BMSCs to enhance their migration towards the injury site, potentially improving the efficacy of stem cell therapies for SCI.

Therapeutic Target

MiR-31 and its downstream targets (CXCR4, MMP-2) could be targeted by novel drugs to promote spinal cord repair.

Clinical Translation

The use of siRNA small molecule nucleic acid drugs such as miR-31 can be translated to clinical treatment of SCI and motor neuron diseases.

Study Limitations

  • 1
    The detailed mechanism of action, particularly whether miR-31 acts on CXCR4/AKT, requires further study.
  • 2
    The long-term effects of miR-31-mediated BMSC migration and SCI repair were not assessed.
  • 3
    This study was conducted in mice, and further research is needed to confirm these findings in larger animal models and eventually in humans.

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