Human dental pulp stem cells--isolation and long term cultivation

• Published in: Acta medica Lékarskí fakulty Univerzity Karlovy v Hradci Králove Vol. 50; no. 3; pp. 195 - 201
• Main Authors: Suchánek, Jakub, Soukup, Tomás, Ivancaková, Romana, Karbanová, Jana, Hubková, Vera, Pytlík, Robert, Kucerová, Lenka
• Format: Journal Article
• Language: English
• Published: Czech Republic Karolinum Press 2007
• Subjects: Adolescent; Adult; Aged; Bone Marrow Cells - cytology; Cell Culture Techniques - methods; Child; Cultivation; Dental pulp; Dental Pulp - cytology; Doubling time; Female; Hayflick’s limit; Humans; Isolation; Male; Mesenchymal Stromal Cells - cytology; Stem cells; Stem Cells - cytology
• ISSN: 1211-4286; 1805-9694
• DOI: 10.14712/18059694.2017.82

Human adult mesenchymal stem cells (MSCs) are rare elements living in various organs (e.g. bone marrow, skeletal muscle), with capability to differentiate in various cell types (e.g. chondrocytes, adipocytes and osteoblasts). In the year 2000, Gronthos and co-workers isolated stem cells from the human dental pulp (DPSCs). Later on, stem cells from exfoliated tooth were also obtained. The aims of our study were to establish protocol of DPSCs isolation and to cultivate DPSCs either from adult or exfoliated tooth, and to compare these cells with mesenchymal progenitor cell (MPCs) cultures. MPCs were isolated from the human bone marrow of proximal femur. DPSCs were isolated from deciduous and permanent teeth. Both cell types were cultivated under the same conditions in the media with 2% of FCS supplemented with PDGF and EGF growth factors. We have cultivated undifferentiated DPSCs for long time, over 60 population doublings in cultivation media designed for bone marrow MPCs. After reaching Hayflick's limit, they still have normal karyotype. Initial doubling time of our cultures was from 12 to 50 hours for first 40 population doublings, after reaching 50 population doublings, doubling time had increased to 60-90 hours. Regression analysis of uncumulated population doublings proved tight dependence of population doublings on passage number and slow decrease of proliferation potential. In comparison with bone marrow MPCs, DPSCs share similar biological characteristics and stem cell properties. The results of our experiments proved that the DPSCs and MPCs are highly proliferative, clonogenic cells that can be expanded beyond Hayflick's limit and remain cytogenetically stable. Moreover we have probably isolated two different populations of DPSCs. These DPSCs lines differed one from another in morphology. Because of their high proliferative and differentiation potential, DPSCs can become more attractive, easily accessible source of adult stem cells for therapeutic purposes.