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Stem Cell Proliferation Pathways Comparison between Human Exfoliated Deciduous Teeth and Dental Pulp Stem Cells by Gene Expression Profile from Promising Dental Pulp

牙髓干细胞 间充质干细胞 干细胞 生物 骨髓 细胞生物学 干细胞标记物 再生医学 干细胞移植修复关节软骨 细胞分化 成体干细胞 癌症研究 免疫学 基因 遗传学
作者
Sayaka Nakamura,Yoichi Yamada,Wataru Katagiri,T Sugito,Kenji Ito,Minoru Ueda
出处
期刊:Journal of Endodontics [Elsevier BV]
卷期号:35 (11): 1536-1542 被引量:223
标识
DOI:10.1016/j.joen.2009.07.024
摘要

Introduction Mesenchymal stem cells (MSCs) have been used for clinical application in tissue engineering and regenerative medicine (TERM). To date, the most common source of MSCs has been bone marrow. However, the bone marrow aspirate is an invasive and painful procedure for the donor. Thus, the identification and characterization of alternative sources of MSCs are of great importance. This study focused on the characterization of stem cells from human exfoliated deciduous teeth (SHED) compared with dental pulp stem cells (DPSCs) and bone marrow–derived mesenchymal stem cells (BMMSCs). Methods We have compared “stemness” such as the proliferation rate and the expression of stem cell marker of DPSCs, SHED, and BMMSCs. In addition, gene expression profile of DPSCs and SHED were analyzed by using DNA microarray. Results All cells isolated from the three sources exhibited MSC characteristics including a fibroblastic morphology, and the expression of mesenchymal stem-cell markers. The proliferation rate of SHED was significantly higher than that of DPSCs and BMMSCs (P < 0.05). The comparison of the gene expression profiles indicated 4386 genes with a changed expression between DPSCs and SHED by 2.0-fold or more. Higher expression in SHED was observed for genes that participate in pathways related to cell proliferation and extracellular matrix, including several cytokines such as fibroblast growth factor and tumor growth factor beta. Conclusions Because of its advantages of a higher proliferation capability, abundant cell supply, and painless stem cell collection with minimal invasion, SHED could be a desirable option as a cell source for potential therapeutic applications.

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