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  4. Grafted human-induced pluripotent stem-cell–derived neurospheres promote motor functional recovery after spinal cord injury in mice

Grafted human-induced pluripotent stem-cell–derived neurospheres promote motor functional recovery after spinal cord injury in mice

PNAS, 2011 · DOI: 10.1073/pnas.1108077108 · Published: October 4, 2011

Spinal Cord InjuryRegenerative MedicineNeurology

Simple Explanation

The study explores the potential of using human-induced pluripotent stem cells (hiPSCs) to treat spinal cord injury (SCI) in mice. hiPSCs are a promising cell source because they don't raise the same ethical concerns as embryonic stem cells. Researchers transplanted neurospheres derived from hiPSCs (hiPSC-NSs) into mice with SCI. These transplanted cells survived, moved within the injured spinal cord, and transformed into different types of neural cells, including neurons, astrocytes, and oligodendrocytes. The transplanted hiPSC-NSs promoted several beneficial effects, such as new blood vessel formation, nerve fiber regrowth, and synapse formation with host neurons. Ultimately, these positive changes led to improved motor function recovery in the mice, without any signs of tumor formation.

Study Duration
112 d
Participants
NOD-SCID mice with spinal cord injury
Evidence Level
Level 2: Experimental study in animal model

Key Findings

  • 1
    Transplanted hiPSC-NSs survived, migrated, and differentiated into neurons, astrocytes, and oligodendrocytes within the injured spinal cord of mice.
  • 2
    hiPSC-NSs promoted angiogenesis, axonal regrowth, and myelination in the injured spinal cord, and formed synapses with host mouse neurons.
  • 3
    Mice treated with hiPSC-NSs showed significantly better motor functional recovery compared to control animals, and this recovery persisted for 112 days post-SCI, with no tumor formation observed.

Research Summary

This study investigated the therapeutic potential of human-induced pluripotent stem cell-derived neurospheres (hiPSC-NSs) for treating spinal cord injury (SCI) in mice. The findings demonstrated that grafted hiPSC-NSs survived, migrated, and differentiated into neural lineages, promoting angiogenesis, axonal regrowth, and synapse formation, leading to improved motor function recovery. The study suggests that hiPSC-NSs are a promising cell source for transplantation therapy for SCI, showing long-term functional recovery without tumor formation in the treated mice.

Practical Implications

Therapeutic Potential for SCI

hiPSC-NS transplantation could become a viable therapeutic option for SCI, offering a cell source without the ethical concerns associated with ESCs.

Improved Functional Recovery

The study highlights the potential for significant improvements in motor function recovery following SCI through hiPSC-NS transplantation.

Enhanced Neuroplasticity

hiPSC-NSs promote neuroplasticity by supporting angiogenesis, axonal regeneration, and synapse formation in the injured spinal cord.

Study Limitations

  • 1
    Study was conducted on NOD-SCID mice
  • 2
    Allodynia was not assessed
  • 3
    Present results are only a first step toward clinical applications

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