PNAS, 2011 · DOI: 10.1073/pnas.1108077108 · Published: October 4, 2011
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.
hiPSC-NS transplantation could become a viable therapeutic option for SCI, offering a cell source without the ethical concerns associated with ESCs.
The study highlights the potential for significant improvements in motor function recovery following SCI through hiPSC-NS transplantation.
hiPSC-NSs promote neuroplasticity by supporting angiogenesis, axonal regeneration, and synapse formation in the injured spinal cord.