Document Type
Article
Language
eng
Format of Original
8 p.
Publication Date
6-2010
Publisher
Human Press
Source Publication
Stem Cell Reviews and Reports
Source ISSN
1550-8943
Original Item ID
DOI: 10.1007/s12015-010-9152-3
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.
Recommended Citation
Hu, Yao Fei; Gourab, Krishnaj; Wells, Clive; Clives, Oliver; Schmit, Brian D.; and Sieber-Blum, Maya, "Epidermal Neural Crest Stem Cell (EPI-NCSC)--Mediated Recovery of Sensory Function in a Mouse Model of Spinal Cord Injury" (2010). Biomedical Engineering Faculty Research and Publications. 309.
https://epublications.marquette.edu/bioengin_fac/309
Comments
Accepted version. Stem Cell Reviews and Reports, Vol. 6, No. 2 (June 2010): 186-198. DOI. © 2010 Humana Press. Used with permission.