Cementum- and periodontal ligament-like tissue formation by dental follicle cell sheets co-cultured with Hertwig's epithelial root sheath cells

被引:100
作者
Bai, Yudi [1 ,2 ,3 ,4 ]
Bai, Yuxiang [5 ]
Matsuzaka, Kenichi [2 ,3 ]
Hashimoto, Sadamitsu [6 ]
Fukuyama, Tatsuro [4 ]
Wu, Lian [1 ]
Miwa, Tsuneyuki [2 ,3 ]
Liu, Xiaohui [1 ]
Wang, Xiaojing [1 ]
Inoue, Takashi [2 ,3 ]
机构
[1] Fourth Mil Med Univ, Sch Stomatol, Dept Pediat Dent, Xian 710032, Peoples R China
[2] Tokyo Dent Coll, Dept Clin Pathophysiol, Mihama Ku, Chiba 2618502, Japan
[3] Tokyo Dent Coll, Oral Hlth Sci Ctr, Mihama Ku, Chiba 2618502, Japan
[4] Tokyo Dent Coll, Dept Pediat Dent, Chiba, Japan
[5] Fourth Mil Med Univ, Dept Hlth Stat, Xian 710032, Peoples R China
[6] Tokyo Dent Coll, Dept Pathol, Chiba, Japan
基金
中国国家自然科学基金;
关键词
Extracellular matrix; Cell sheet; Co-culture; Dental follicle cell; Hertwig's epithelial root sheath; ENAMEL MATRIX; GAP-JUNCTIONS; STEM-CELLS; IN-VITRO; DIFFERENTIATION; EXPRESSION; VIVO; CEMENTOBLASTS; REGENERATION; PHENOTYPE;
D O I
10.1016/j.bone.2011.02.016
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Dental follicle cells (DFCs) are believed contain the precursor cells of the periodontium and can form cell sheets by secreting extracellular matrix (ECM) proteins. Cell sheet engineering has been recently developed and applied successfully in the field of tissue regeneration. However, research on the in vitro characteristics of DFC sheets is lacking and an assessment of whether DFC sheets can produce periodontal tissues in vivo has not been reported. To test the characteristics and applicability of DFC sheets in this field, we established a co-culture system of rat DFCs and Hertwig's epithelial root sheath (HERS) cells in vitro, and included the following controls: a co-culture of DFCs and alveolar mucosa epithelial cells, DFCs with no cells in the upper chamber, and DFCs cultured without an upper chamber. After 3 weeks of co-culturing the cells, the DFC sheets were transplanted into adult male rats' omenta. One week after co-culturing DFCs with HERS cells, mRNA levels of collagen type I (COL-1), alkaline phosphatase (ALP), runt related transcription factor 2 (Runx 2) and bone sialoprotein (BSP) were increased significantly. In addition, after 3 weeks of co-culturing the cells, the numbers of ALP-, osteocalcin (OCN)-, BSP- and osteoprotegerin (OPG)-positive DFCs increased. The DFCs also produced more calcified nodules and exhibited an increased number of subcellular organelles, which are important for protein synthesis and secretion. Moreover, gap junctions were found between the experimental DFCs within the sheet. Five weeks of in vivo growth of DFC sheets pre-exposed to HERS cells led to the formation of cementum-like tissues, which were positive for OCN, BSP and OPG, as well as the formation of periodontal ligament-like tissues, which were positive for COL-1. In contrast, control cells only produced fibrous tissues. These results indicate that the DFC sheets induced by HERS cells are able to produce periodontal tissues through epithelial-mesenchymal interactions. Therefore, DFC sheets may be useful in the field of periodontium regeneration. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:1417 / 1426
页数:10
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