Modification of Pluripotency and Neural Crest-Related Genes' expression in Murine Skin-Derived Precursor Cells by Leukemia Inhibitory Factor (LIF).
- Author:
Sang Kyu PARK
1
;
Sangho ROH
Author Information
1. Cellular Reprogramming and Embryo Biotechnology Laboratory, Dental Research Institute, and CLS21, Seoul National University School of Dentistry, Seoul, Korea. sangho@snu.ac.kr
- Publication Type:Original Article
- Keywords:
Skin precursor cell;
Leukemia inhibitory factor;
Oct4;
Nanog;
Ngfr
- MeSH:
Adult Stem Cells;
Animals;
Cell Proliferation;
Dermis;
Durapatite;
Embryonic Stem Cells;
Leukemia;
Leukemia Inhibitory Factor;
Mesenchymal Stromal Cells;
Mice;
Neural Crest;
Pluripotent Stem Cells
- From:International Journal of Oral Biology
2012;37(4):175-180
- CountryRepublic of Korea
- Language:English
-
Abstract:
Skin-derived precursor cells (SKPs) are multipotent, sphere-forming and embryonic neural crest-related precursor cells that can be isolated from dermis. It is known that the properties of porcine SKPs can be enhanced by leukemia inhibitory factor (LIF) which is an essential factor for the generation of embryonic stem cells in mice. In our present study, to enhance or maintain the properties of murine SKPs, LIF was added to the culture medium. SKPs were treated with 1,000 IU LIF for 72 hours after passage 3. Quantitative real time RT-PCR was then performed to quantify the expression of the pluripotent stem cell specific genes Oct4, Nanog, Klf4 and c-Myc, and the neural crest specific genes Snai2 and Ngfr. The results show that the expression of Oct4 is increased in murine SKPs by LIF treatment whereas the level of Ngfr is decreased under these conditions. Interestingly, LIF treatment reduced Nanog expression which is also important for cell proliferation in adult stem cells and for osteogenic induction in mesenchymal stem cells. These findings implicate LIF in the maintenance of stemness in SKPs through the suppression of lineage differentiation and in part through the control of cell proliferation.
