A comparison study of dental pulp stem cells derived from healthy and orthodontically intruded human permanent teeth for mesenchymal stem cell characterisation.
May Nak LauWijenthiran KunasekaranYue Yuan OnLi Jin TanNurshafiqah Athirah ZaharinSarah H A GhaniSabri MusaRoziana M RaziGokula MohanPublished in: PloS one (2022)
The objective of this study was to compare the characteristics of Dental Pulp Stem Cells (DPSCs) derived from healthy human permanent teeth with those that were orthodontically-intruded to serve as potential Mesenchymal Stem Cells (MSC). Recruited subjects were treated with orthodontic intrusion on one side of the maxillary first premolar while the opposite side served as the control for a period of six weeks before the dental pulp was extracted. Isolated DPSCs from both the control and intruded samples were analyzed, looking at the morphology, growth kinetics, cell surface marker profile, and multilineage differentiation for MSC characterisation. Our study showed that cells isolated from both groups were able to attach to the cell culture flask, exhibited fibroblast-like morphology under light microscopy, able to differentiate into osteogenic, adipogenic and chondrogenic lineages as well as tested positive for MSCs cell surface markers CD90 and CD105 but negative for haematopoietic cell surface markers CD34 and HLA-DR. Both groups displayed a trend of gradually increasing population doubling time from passage 1 to passage 5. Viable DPSCs from both groups were successfully recovered from their cryopreserved state. In conclusion, DPSCs in the dental pulp of upper premolar not only remained viable after 6 weeks of orthodontic intrusion using fixed appliances but also able to develop into MSCs.
Keyphrases
- mesenchymal stem cells
- cell surface
- umbilical cord
- stem cells
- cell therapy
- endothelial cells
- bone marrow
- induced apoptosis
- induced pluripotent stem cells
- pluripotent stem cells
- high resolution
- optical coherence tomography
- cell cycle arrest
- oral health
- gestational age
- risk assessment
- cell proliferation
- signaling pathway
- newly diagnosed
- human health
- oxidative stress