Comparative characterization of stem cells from human exfoliated deciduous teeth and dental pulp stem cells

被引:149
|
作者
Wang, Xi [1 ,2 ]
Sha, Xin-Jia [3 ]
Li, Guang-Hui [4 ]
Yang, Fu-Sheng [1 ]
Ji, Kun [1 ]
Wen, Ling-Ying [1 ]
Liu, Shi-Yu [2 ]
Chen, Lei [5 ]
Ding, Yin [2 ]
Xuan, Kun [1 ]
机构
[1] Fourth Mil Med Univ, Sch Stomatol, Dept Pediat Dent, Xian 710032, Shaanxi, Peoples R China
[2] Fourth Mil Med Univ, Sch Stomatol, Dept Orthodont, Xian 710032, Shaanxi, Peoples R China
[3] Fourth Mil Med Univ, Res & Dev Ctr Tissue Engn, Xian 710032, Shaanxi, Peoples R China
[4] Fourth Mil Med Univ, Sch Stomatol, Dept Oral & Maxillofacial Surg, Xian 710032, Shaanxi, Peoples R China
[5] Jinan Stomatol Hosp, Dept Orthodont, Jinan 250001, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Stem cells from human exfoliated deciduous teeth (SHED); Dental pulp stem cells (DPSCs); Proliferation rate; Osteogenic differentiation; Cell sheet; GENE-EXPRESSION; VITAMIN-C; IN-VITRO; DIFFERENTIATION; REPAIR; CRYOPRESERVATION; FIBROBLASTS; DPSCS; VIVO;
D O I
10.1016/j.archoralbio.2012.02.014
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: This study focused on the characterization of stem cells from human exfoliated deciduous teeth (SHED) in comparison with dental pulp stem cells (DPSCs) to certify SHED as a key element in tissue engineering. Methods: In the present study, SHED and DPSCs were assayed for their cell surface antigens and proliferation by measuring the cell cycles, growth rates, Ki67-positive efficiencies, and colony-forming units (CFUs). The evaluation of multi-differentiation was performed using alizarin red and oil red O and real-time PCR in vitro. The mineralization capability of the cells was examined in vivo by implanting with ceramic bovine bone (CBB) into subcutaneous of immunocompromised mice for 8 weeks. A three-dimensional pellet cultivation system is proposed for SHED and DPSCs to recreate the biological microenvironment that is similar to that of a regenerative milieu. Results: SHED showed a higher proliferation rate and differentiation capability in comparison with DPSCs in vitro, and the results of the in vivo transplantation suggest that SHED have a higher capability of mineralization than the DPSCs. The mRNA expression levels of inflammatory cytokines, including matrix metalloproteinase-1 (MMP1), tissue inhibitors of metalloproteinase-1 (TIMP1), matrix metalloproteinase-2 (MMP2), tissue inhibitors of metalloproteinase-2 (TIMP2) and interleukin-6 (IL-6) were higher in SHED than that in DPSCs. In addition, the expression levels of Col l and proliferating cell nuclear antigen (PCNA) in SHED sheets were significantly higher than those in DPSCs sheets. Conclusions: This study systematically demonstrated the differences in the growth and differentiation characteristics between SHED and DPSCs. Consequently, SHED may represent a suitable, accessible and potential alternative source for regenerative medicine and therapeutic applications. Crown Copyright (C) 2012 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1231 / 1240
页数:10
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