Title |
Human Epidermal Neural Crest Stem Cells (hEPI-NCSC)—Characterization and Directed Differentiation into Osteocytes and Melanocytes
|
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Published in |
Stem Cell Reviews and Reports, April 2011
|
DOI | 10.1007/s12015-011-9255-5 |
Pubmed ID | |
Authors |
Oliver Clewes, Alla Narytnyk, Kevin R. Gillinder, Andrew D. Loughney, Alison P. Murdoch, Maya Sieber-Blum |
Abstract |
Here we describe the isolation, characterisation and ex-vivo expansion of human epidermal neural crest stem cells (hEPI-NCSC) and we provide protocols for their directed differentiation into osteocytes and melanocytes. hEPI-NCSC are neural crest-derived multipotent stem cells that persist into adulthood in the bulge of hair follicles. Multipotency and self-renewal were determined by in vitro clonal analyses. hEPI-NCSC generate all major neural crest derivatives, including bone/cartilage cells, neurons, Schwann cells, myofibroblasts and melanocytes. Furthermore, hEPI-NCSC express additional neural crest stem cell markers and global stem cell genes. To variable degrees and in a donor-dependent manner, hEPI-NCSC express the six essential pluripotency genes C-MYC, KLF4, SOX2, LIN28, OCT-4/POU5F1 and NANOG. hEPI-NCSC can be expanded ex vivo into millions of stem cells that remain mulitpotent and continue to express stem cell genes. The novelty of hEPI-NCSC lies in the combination of their highly desirable traits. hEPI-NCSC are embryonic remnants in a postnatal location, the bulge of hair follicles. Therefore they are readily accessible in the hairy skin by minimal invasive procedure. hEPI-NCSC are multipotent somatic stem cells that can be isolated reproducibly and with high yield. By taking advantage of their migratory ability, hEPI-NCSC can be isolated as a highly pure population of stem cells. hEPI-NCSC can undergo robust ex vivo expansion and directed differentiation. As somatic stem cells, hEPI-NCSC are conducive to autologous transplantation, which avoids graft rejection. Together, these traits make hEPI-NCSC novel and attractive candidates for future cell-based therapies and regenerative medicine. |
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Geographical breakdown
Country | Count | As % |
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United Kingdom | 2 | 2% |
Netherlands | 1 | 1% |
Canada | 1 | 1% |
China | 1 | 1% |
Japan | 1 | 1% |
Unknown | 90 | 94% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Ph. D. Student | 23 | 24% |
Researcher | 22 | 23% |
Student > Master | 10 | 10% |
Student > Bachelor | 10 | 10% |
Student > Doctoral Student | 5 | 5% |
Other | 15 | 16% |
Unknown | 11 | 11% |
Readers by discipline | Count | As % |
---|---|---|
Agricultural and Biological Sciences | 42 | 44% |
Biochemistry, Genetics and Molecular Biology | 18 | 19% |
Medicine and Dentistry | 15 | 16% |
Neuroscience | 5 | 5% |
Engineering | 2 | 2% |
Other | 3 | 3% |
Unknown | 11 | 11% |