Recently, several studies have demonstrated that periodontal ligament (PDL) cells differentiate into cementoblastic cells and adipogenic cells
in vitro. Therefore, the PDL probably contains pluripotent progenitor cells or putative stem cells. Until now, bone-marrow-derived MSCs (BMMSCs) are good candidates for the treatment of mesenchymal tissue as a source of cells for cell-based therapeutic strategies. Although BMMSCs are very usuful for clinical applications, bone marrow aspiration for MSCs extraction is an invasive and painful procedure for the donor. In addition, the number, proliferation and differentiation potential of BMMSCs decline with increasing age. However, isolating MSCs derived from PDL tissue of deciduous tooth can be non-invasive and economical procedure when permanent tooth replace deciduous tooth.Therefore, it has been thought that PDL cell line from deciduous teeth could be useful tool for the investigation of regenerative medicine. Nevertheless, clonal PDL cell lines have not been established from deciduous teeth.Here, we used human telomerase reverse transcriptase (
hTERT) induction to establish the first immortalized PDL cell lines derived from deciduous teeth. We successfully obtained 3 single-cell clones, and named them single cell derived from human deciduous PDL (SH) 9, 10 and 11. All the SH cells showed
hTERT expression and stable proliferation after >80 population doublings and expressed the marker genes of PDL cells, including scleraxis, periostin, cementum-derived protein 23,and tenomodulin. Although all the clones expressed osteoblastic markers, only the clones from the SH9 cell line differentiated into mature osteoblastic cells which could form calcified nodules
in vitro. Recent study have showed that stromal cell-derived factor (SDF)-1
α play a crucial role in stem cell homing and recruitment to injured sites. However, no information is available about SDF-1
α in periodontal tissues. The second aim of this study was to evaluate whether fibroblast growth factor (FGF)-2 and transforming growth factor (TGF)-
β1 could affect SDF-1
α expression by immortalized PDL cells derived from deciduous tooth (SH 9 cells)
in vitro. FGF-2 inhibited SDF-1
α expression at about 10% of control by 48 h, TGF-
β1 induced it at about 6 fold of control between 6 h and 12 h after treatment. These results suggested that SDF-1
α produced by PDL might play an important role in adult stem cell and progenitor cell release, recruitment and homing to injury sites.This is the review of the immortalization of PDL cells derived from deciduous teeth and the regulation of SDF-1
α expression in PDL cells with FGF-2 and TGF-
β1. These cells could be useful in studies investigating the cellular mechanisms and regenerative processes of human PDL cells.
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