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RESEARCH PRODUCT

Growth kinetics and characterization of human dental pulp stem cells: Comparison between third molar and first premolar teeth

Parisa MahdiyarDavood MehrabaniShahrokh ZareAmin TamadonMehdi DianatpourReza RobatiKianoosh Torabi

subject

MolarCD34DentistryOdontologíaOperative Dentistry and EndodonticsAndrology030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicinestomatognathic systemTissue engineeringDental pulp stem cellsPremolarmedicineCD90General Dentistrybusiness.industryChemistryResearchMesenchymal stem cell030206 dentistry:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludstomatognathic diseasesmedicine.anatomical_structureUNESCO::CIENCIAS MÉDICASStem cellbusiness

description

Background Dental pulp stem cells (DPSCs) play an important role in tissue regeneration. This study compares the growth kinetics and characterization of third molar and first premolar human DPSCs. Material and Methods Dental pulp tissues were isolated from human first premolar and third molar teeth and were digested by treating them with collagenase type I. Single-cell suspensions from each dental pulp were seeded in T25 culture flasks and the media were replaced every 3 days until 70% confluence. The cells were enumerated to determine the population doubling time (PDT). Cells were characterized using flow cytometry, RT-PCR and osteogenic medium for differentiation of DPSCs. Karyotyping assay was also performed till passage 7th. Results The DPSCs had spindle-shaped morphology. There was an increase in PDT in third molar DPSCs when compared to first premolar teeth. Positive expression of CD44, CD73, and CD90 and negative expression of CD34 and CD45 were illustrated. A normal karyotype was visible for all seven passages. The Alizarin red staining was positive for osteogenic induction of DPSCs. Conclusions When DPSCs are needed, third molar teeth can be a good and convenient candidate for cell transplantation, yielding high number of cells with mesenchymal characteristics. They can be a source for further investigations in vitro and work on tissue engineering protocols. Key words:Stem cells, dental pulp, growth kinetics, characterization.

https://doi.org/10.4317/jced.52824