Inherent Differential Propensity of Dental Pulp Stem Cells Derived from Human Deciduous and Permanent Teeth

被引:135
作者
Govindasamy, Vijayendran [4 ]
Abdullah, Aimi Naim [2 ]
Ronald, Veronica Sainik [2 ]
Musa, Sabri [2 ]
Ab Aziz, Zeti Adura Che [1 ]
Zain, Rosnah Binti [3 ]
Totey, Satish [4 ]
Bhonde, Ramesh R. [4 ]
Abu Kasim, Noor Hayaty [1 ]
机构
[1] Univ Malaya, Fac Dent, Dept Conservat Dent, Kuala Lumpur 50603, Malaysia
[2] Univ Malaya, Fac Dent, Dept Childrens Dent & Orthodont, Kuala Lumpur 50603, Malaysia
[3] Univ Malaya, Fac Dent, Dept Oral Pathol Oral Med& Periodontol, OCRCC, Kuala Lumpur 50603, Malaysia
[4] Stempeut Res Malaysia Sdn Bhd, Kuala Lumpur, Malaysia
关键词
Deciduous teeth; dental pulp stem cells; inherent propensity; permanent teeth; IN-VITRO; EXPRESSION; MARROW; PLURIPOTENCY; GENERATION; POPULATION; THERAPY; NEURONS; NESTIN; TISSUE;
D O I
10.1016/j.joen.2010.05.006
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: Lately, several new stem cell sources and their effective isolation have been reported that claim to have potential for therapeutic applications. However, it is not yet clear which type of stem cell sources are most potent and best for targeted therapy. Lack of understanding of nature of these cells and their lineage-specific propensity might hinder their full potential. Therefore, understanding the gene expression profile that indicates their lineage-specific proclivity is fundamental to the development of successful cell-based therapies. Methods: We compared proliferation rate, gene expression profile, and lineage-specific propensity of stem cells derived from human deciduous (SCD) and permanent teeth (DPSCs) over 5 passages. Results: The proliferation rate of SCD was higher (cell number, 25 x 10(6) cells/mL; percent colony-forming units [CFUs], 151.67 +/- 10.5; percent cells in S/G2 phase, 12.4 +/- 1.48) than that of DPSCs (cell number, 21 x 10(6) cells/mL; percent CFUs, 133 +/- 17.62; percent cells in S/G2 phase, 10.4 +/- 1.18). It was observed that fold expression of several pluripotent markers such as OCT4, SOX2, NANOG, and REX1 were higher (>2) in SCD as compared with DPSCs. However, DPSCs showed higher expression of neuroectodermal markers PAX6, GBX2, and nestin (fold expression >100). Similarly, higher neurosphere formation and neuronal marker expression (NF, GFAP) were found in the differentiated DPSCs into neuron-like cells as compared with SCD. Conclusions: This study thus demonstrates that both SCD and DPSCs exhibit specific gene expression profile, with clear-cut inclination of DPSCs toward neuronal lineage. (J Endod 2010;36:1504-1515)
引用
收藏
页码:1504 / 1515
页数:12
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