J Neurosci Res, 2019 · DOI: 10.1002/jnr.24351 · Published: February 1, 2019
Transplanting neural progenitor cells is a promising approach for repairing the injured central nervous system. Early studies showed that transplanting embryonic spinal cord tissue could facilitate repair, leading to clinical studies in patients with spinal cord injuries. These early studies also analyzed the structure of the transplanted tissue to understand how it promotes repair, revealing a mix of neurons and glia that become vascularized and maintain spinal cord morphology. Current research focuses on identifying specific interneuronal phenotypes within donor tissues that could be optimal for transplantation, particularly ventrally-derived phenotypes, which are associated with motor functions.
V2a SpINs, as excitatory pre-motor interneurons, could improve motor function in SCI and ALS models.
Identifying optimal donor cells for transplantation could lead to more effective therapies for spinal cord repair.
Transplanted spinal interneurons (SpINs) are key cellular elements for neuroplasticity after injury and may represent an important therapeutic target.