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Epidermal neural crest stem cell (EPI-NCSC)--mediated recovery of sensory function in a mouse model of spinal cord injury. Stem Cell Rev Rep 2010 Jun;6(2):186-98

Date

04/24/2010

Pubmed ID

20414748

Pubmed Central ID

PMC2887506

DOI

10.1007/s12015-010-9152-3

Scopus ID

2-s2.0-77953914847 (requires institutional sign-in at Scopus site)   67 Citations

Abstract

Here we show that epidermal neural crest stem cell (EPI-NCSC) transplants in the contused spinal cord caused a 24% improvement in sensory connectivity and a substantial recovery of touch perception. Furthermore we present a novel method for the ex vivo expansion of EPI-NCSC into millions of stem cells that takes advantage of the migratory ability of neural crest stem cells and is based on a new culture medium and the use of microcarriers. Functional improvement was shown by two independent methods, spinal somatosensory evoked potentials (SpSEP) and the Semmes-Weinstein touch test. Subsets of transplanted cells differentiated into myelinating oligodendrocytes. Unilateral injections of EPI-NCSC into the lesion of midline contused mouse spinal cords elicited bilateral improvements. Intraspinal EPI-NCSC did not migrate laterally in the spinal cord or invade the spinal roots and dorsal root ganglia, thus implicating diffusible factors. EPI-NCSC expressed neurotrophic factors, angiogenic factors, and metalloproteases. The strength of EPI-NCSC thus is that they can exert a combination of pertinent functions in the contused spinal cord, including cell replacement, neuroprotection, angiogenesis and modulation of scar formation. EPI-NCSC are uniquely qualified for cell-based therapy in spinal cord injury, as neural crest cells and neural tube stem cells share a higher order stem cell and are thus ontologically closely related.

Author List

Hu YF, Gourab K, Wells C, Clewes O, Schmit BD, Sieber-Blum M

Author

Brian Schmit PhD Professor in the Biomedical Engineering department at Marquette University




MESH terms used to index this publication - Major topics in bold

Animals
Evoked Potentials, Somatosensory
Mice
Mice, Inbred C57BL
Mice, Mutant Strains
Microscopy, Electron, Transmission
Models, Biological
Neural Crest
Polymerase Chain Reaction
Spinal Cord
Spinal Cord Injuries
Stem Cell Transplantation
Stem Cells