Cultivation of Cryopreserved Human Dental Pulp Stem Cells-A New Approach to Maintaining Dental Pulp Tissue

Int J Mol Sci. 2022 Sep 29;23(19):11485. doi: 10.3390/ijms231911485.

Abstract

Human dental pulp stem cells (hDPSCs) are multipotent mesenchymal stem cells (MSCs) that are capable of self-renewal with multilineage differentiation potential. After being cryopreserved, hDPSCs were reported to maintain a high level of proliferation and multi-differentiation abilities. In order to optimize cryopreservation techniques, decrease storage requirements and lower contamination risks, the feasibility of new whole-tooth cryopreservation and its effects on hDPSCs were tested. The survival rates, morphology, proliferation rates, cell activity, surface antigens and differentiation abilities of hDPSCs isolated from fresh teeth were compared with those of one-month cryopreserved teeth in 5% and 10% DMSO. The data of the present study indicated that the new cryopreservation approach did not reduce the capabilities or stemness of hDPSCs, with the exception that it extended the first appearance time of hDPSCs in the teeth that were cryopreserved in 10% DMSO, and reduced their recovery rate. With the novel strategy of freezing, the hDPSCs still expressed the typical surface markers of MSCs and maintained excellent proliferation capacity. Three consecutive weeks of osteogenic and adipogenic induction also showed that the expression of the key genes in hDPSCs, including lipoprotein lipase (LPL), peroxisome proliferator-activated receptor-γ (PPAR-γ), alkaline phosphatase (ALP), runt-related transcription factor 2 (RUNX2), type I collagen (COL I) and osteocalcin (OSC) was not affected, indicating that their differentiation abilities remained intact, which are crucial parameters for hDPSCs as cell-therapy candidates. These results demonstrated that the new cryopreservation method is low-cost and effective for the good preservation of hDPSCs without compromising cell performance, and can provide ideas and evidence for the future application of stem-cell therapies and the establishment of dental banks.

Keywords: cellular differentiation; cryopreservation; dimethyl sulfoxide; human dental pulp stem cells; methodology; teeth.

MeSH terms

  • Alkaline Phosphatase / metabolism
  • Antigens, Surface / metabolism
  • Cell Differentiation
  • Cell Proliferation
  • Cells, Cultured
  • Collagen Type I / metabolism
  • Core Binding Factor Alpha 1 Subunit* / metabolism
  • Cryopreservation / methods
  • Dental Pulp / metabolism
  • Dimethyl Sulfoxide / metabolism
  • Humans
  • Lipoprotein Lipase* / metabolism
  • Osteocalcin / genetics
  • Osteocalcin / metabolism
  • Osteogenesis
  • Peroxisome Proliferator-Activated Receptors / metabolism
  • Stem Cells / metabolism

Substances

  • Antigens, Surface
  • Collagen Type I
  • Core Binding Factor Alpha 1 Subunit
  • Peroxisome Proliferator-Activated Receptors
  • Osteocalcin
  • Lipoprotein Lipase
  • Alkaline Phosphatase
  • Dimethyl Sulfoxide

Grants and funding

This research was funded by Merit Scholarship for International Students, grant number No.7238065.