Gene Expression Profile of Dental Pulp Cells During Differentiation Into an Adipocyte Lineage
Gene Expression Profile of Dental Pulp Cells During Differentiation Into an Adipocyte Lineage
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DOI:
10.1254/jphs.10163fp
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发表时间:
2011-03-01
影响因子:
3.5
通讯作者:
Ohura, Kiyoshi
中科院分区:
文献类型:
--
作者:
Nozaki, Tadashige;Ohura, Kiyoshi
Gene regulation during in vitro differentiation into adipocytes was examined in dental pulp derived cells. Insulin, 3-isobutyl-1-methylxanthine, and dexamethasone were added to induce adipogenesis. Cells containing lipid droplets were observed after induction as in 3T3 L 1 cells. Rat dental pulp derived cells showed their potential to differentiate into adipocytes in vitro. In both types of cells, the pluripotent markers Oct-3/4 and Sox2 were downregulated during differentiation, whereas the expression of Nanog was not significantly changed during differentiation. Interestingly, in the dental pulp derived cells, the level of Oct-3/4 was transiently induced at I week after induction and then significantly decreased during differentiation. Based on the expression profiles determined using GeneChip Arrays, 3418 probes across 10 clusters showed a difference in expression at 1, 2, and 3 weeks after induction versus before induction. Notably, genes in the PPAR signaling pathway including Ppar gamma, Fabp4, and the C/EBP family were upregulated by more than 3-fold. Upregulation of the PPAR pathways seems to be a critical signal transduction pathway in this differentiation system. These findings indicate that dental pulp derived cells are a potential source of adipogenic cells, and their gene expression profile could be useful in future regenerative medicine applications.