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  4. IPSC-Derived Sensory Neurons Directing Fate Commitment of Human BMSC-Derived Schwann Cells: Applications in Traumatic Neural Injuries

IPSC-Derived Sensory Neurons Directing Fate Commitment of Human BMSC-Derived Schwann Cells: Applications in Traumatic Neural Injuries

Cells, 2023 · DOI: 10.3390/cells12111479 · Published: May 25, 2023

Regenerative MedicineNeurologyGenetics

Simple Explanation

This study explores using human bone marrow stem cells (hBMSCs) to create Schwann cells, which are crucial for nerve regeneration after injury. The researchers used sensory neurons derived from induced pluripotent stem cells (iPSCs) to guide the development of hBMSCs into specialized Schwann cells (hBMSC-dSCs). These hBMSC-dSCs were then tested in rat models of sciatic nerve and spinal cord injuries to see if they could help repair damaged nerves and improve motor function.

Study Duration
12 weeks
Participants
Adult male SD rats (220–250 g)
Evidence Level
Not specified

Key Findings

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    hBMSC-dSCs, when transplanted into rats with sciatic nerve injuries, significantly improved gait compared to controls, suggesting nerve regeneration.
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    In rats with spinal cord injuries, hBMSC-dSCs combined with chondroitinase ABC (ChABC) led to significant improvements in hindlimb motor function.
  • 3
    Microscopic analysis confirmed that hBMSC-dSCs were capable of myelinating axons (forming a protective sheath around nerve fibers) in both peripheral and central nervous system injury models.

Research Summary

The study demonstrates a method for generating fate-committed Schwann cells from human bone marrow stromal cells (hBMSCs) using induced pluripotent stem-cell-derived sensory neurons (hiSNs). Transplantation of these hBMSC-derived Schwann cells (hBMSC-dSCs) into rat models of sciatic nerve injury and spinal cord injury showed significant improvements in nerve regeneration and motor function recovery. The results suggest that hBMSC-dSCs hold promise for autologous transplantation therapies aimed at remyelination and functional recovery after traumatic injuries to both the peripheral and central nervous systems.

Practical Implications

Clinical Translation Potential

The study provides a protocol for generating fate-committed Schwann cells from a patient's own bone marrow, reducing the risk of immune rejection in transplantation therapies.

Combination Therapies

The research highlights the potential of combining cell transplantation with other therapeutic interventions, such as ChABC treatment, to enhance nerve regeneration and functional recovery.

Improved Treatment Strategies

The findings contribute to the development of more effective strategies for treating traumatic nerve injuries in both the peripheral and central nervous systems.

Study Limitations

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