| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3150139 | Journal of Endodontics | 2016 | 6 Pages |
•We isolated dental pulp stem cells (DPSCs) from fresh and cryopreserved pulp gained from endodontic treatment.•We characterized DPSCs of these 2 groups and compared them with each other.•Dental pulp can be cryopreserved without losing normal properties of their DPSCs.•Cryopreservation of inflamed pulp tissues is a retrievable DPSC source.•Our preliminary data facilitate the development of future current Good Tissue Practice (cGTP) protocols.
IntroductionHuman dental pulp stem cells (DPSCs) are becoming an attractive target for therapeutic purposes because of their neural crest origin and propensity. Although DPSCs can be successfully cryopreserved, there are hardly any reports on cryopreservation of dental pulp tissues obtained from teeth diagnosed with symptomatic irreversible pulpitis during endodontic treatment and isolation and characterization of DPSCs from such cryopreserved pulp. The aim of this study was to cryopreserve the said pulp tissues to propagate and characterize isolated DPSCs.MethodsA medium consisting of 90% fetal bovine serum and 10% dimethyl sulfoxide was used for cryopreservation of pulp tissues. DPSCs were isolated from fresh and cryopreserved pulp tissues using an enzymatic method. Cell viability and proliferation were determined using the MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assay. DPSC migration and interaction were analyzed with the wound healing assay. Mesenchymal characteristics of DPSCs were verified by flow cytometric analysis of cell surface CD markers. The osteogenic and adipogenic potential of DPSCs was shown by von Kossa and oil red O staining methods, respectively, and the polymerase chain reaction method.ResultWe found no significant difference in CD marker expression and osteogenic and adipogenic differentiation potential of DPSCs obtained from fresh and cryopreserved dental pulp tissue.ConclusionsOur study shows that dental pulp can be successfully cryopreserved without losing normal characteristics and differentiation potential of their DPSCs, thus making them suitable for dental banking and future therapeutic purposes.
