Human neural stem cells differentiate and promote locomotor recovery in spinal cord-injured mice

B. Cummings(Salk Institute for Biological Studies), Nobuko Uchida(Salk Institute for Biological Studies), Stanley Tamaki(Salk Institute for Biological Studies), Desirée L. Salazar(Salk Institute for Biological Studies), Mitra J. Hooshmand(Salk Institute for Biological Studies), Robert G. Summers(Salk Institute for Biological Studies), Fred H. Gage(Salk Institute for Biological Studies), Aileen J. Anderson(Salk Institute for Biological Studies)
Proceedings of the National Academy of Sciences
September 19, 2005
Cited by 722Open Access
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Abstract

We report that prospectively isolated, human CNS stem cells grown as neurospheres (hCNS-SCns) survive, migrate, and express differentiation markers for neurons and oligodendrocytes after long-term engraftment in spinal cord-injured NOD-scid mice. hCNS-SCns engraftment was associated with locomotor recovery, an observation that was abolished by selective ablation of engrafted cells by diphtheria toxin. Remyelination by hCNS-SCns was found in both the spinal cord injury NOD-scid model and myelin-deficient shiverer mice. Moreover, electron microscopic evidence consistent with synapse formation between hCNS-SCns and mouse host neurons was observed. Glial fibrillary acidic protein-positive astrocytic differentiation was rare, and hCNS-SCns did not appear to contribute to the scar. These data suggest that hCNS-SCns may possess therapeutic potential for CNS injury and disease.


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