Comparison of osteo/odontogenic differentiation of human adult dental pulp stem cells and stem cells from apical papilla in the presence of platelet lysate

被引:50
作者
Abuarqoub, Duaa [1 ]
Awidi, Abdalla [1 ]
Abuharfeil, Nizar [2 ]
机构
[1] Univ Jordan, Fac Med, Cell Therapy Ctr, Amman, Jordan
[2] Jordan Univ Sci & Technol, Dept Appl Biol, Irbid, Jordan
关键词
Dental stem cells; DPSC; SCAP; Platelet lysate; MESENCHYMAL STROMAL CELLS; HUMAN UMBILICAL-CORD; FETAL BOVINE SERUM; OSTEOGENIC DIFFERENTIATION; IN-VITRO; BONE; EXPANSION; GROWTH; PROLIFERATION; THERAPY;
D O I
10.1016/j.archoralbio.2015.07.007
中图分类号
R78 [口腔科学];
学科分类号
100302 [口腔临床医学];
摘要
Introduction: Human dental pulp cells (DPSCs) and stem cells from apical papilla have been used for the repair of damaged tooth tissues. Human platelet lysate (PL) has been suggested as a substitute for fetal bovine serum (FBS) for large scale expansion of dental stem cells. However, biological effects and optimal concentrations of PL for proliferation and differentiation of human dental stem cells remain to be elucidated. Methodology: DPSCs and SCAP cells were isolated from impacted third molars of young healthy donors, at the stage of root development and identified by markers using flow cytometry. For comparison the cells were cultured in media containing PL (1%, 5% and 10%) and FBS, with subsequent induction for osteogenic/odontogenic differentiation. The cultures were analyzed for; morphology, growth characteristics, mineralization potential (Alizarin Red method) and differentiation markers using ELISA and real time -polymerase chain reaction (qPCR). Results: The proliferation rates of DPSCs and SCAP significantly increased when cells were treated with 5% PL (7X doubling time) as compared to FBS. 5% PL also enhanced mineralized differentiation of DPSCs and SCAP, as indicated by the measurement of alkaline phosphatase activity, osteocalcin and osteopontin, calcium deposition and q-PCR. Conclusion: Our findings suggest that using 5% platelet lysate, proliferation and osteo/odontogenesis of DPSCs and SCAP for a short period of time (15 days), was significantly improved. This may imply its use as an optimum concentration for expansion of dental stem cells in bone regeneration. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1545 / 1553
页数:9
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