Novel biological activity of ameloblastin in enamel matrix derivative

被引:2
|
作者
Kuramitsu-Fujimoto, Sachiko [1 ]
Ariyoshi, Wataru [2 ]
Saito, Noriko [3 ]
Okinaga, Toshinori [2 ]
Kamo, Masaharu [4 ]
Ishisaki, Akira [4 ]
Takata, Takashi [5 ]
Yamaguchi, Kazunori [1 ]
Nishihara, Tatsuji [2 ]
机构
[1] Kyushu Dent Univ, Dept Growth Dev Funct, Div Orofacial Funct & Orthodont, Fukuoka, Japan
[2] Kyushu Dent Univ, Dept Hlth Promot, Div Infect & Mol Biol, Fukuoka, Japan
[3] Kyushu Dent Univ, Dept Cariol & Periodontol, Div Pulp Biol Operat Dent & Endodont, Fukuoka, Japan
[4] Iwate Med Univ, Dept Biochem, Div Cellular Biosignal Sci, Morioka, Iwate, Japan
[5] Hiroshima Univ, Inst Biomed & Hlth Sci, Dept Oral & Maxillofacial Pathobiol, Hiroshima, Japan
关键词
Periodontitis; Periodontal guided tissue regeneration; Epithelial cells; Dental enamel proteins; IN-VITRO; CALCIUM-BINDING; CELLS; PROLIFERATION; PROTEINS; GENE;
D O I
10.1590/1678-775720140291
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: Enamel matrix derivative (EMD) is used clinically to promote periodontal tissue regeneration. However, the effects of EMD on gingival epithelial cells during regeneration of periodontal tissues are unclear. In this in vitro study, we purified ameloblastin from EMD and investigated its biological effects on epithelial cells. Material and Methods: Bioactive fractions were purified from EMD by reversed-phase high-performance liquid chromatography using hydrophobic support with a C18 column. The mouse gingival epithelial cell line GE-1 and human oral squamous cell carcinoma line SCC-25 were treated with purified EMD fraction, and cell survival was assessed with a WST-1 assay. To identify the proteins in bioactive fractions of EMD, we used proteome analysis with two-dimensional gel electrophoresis followed by identification with liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis. Results: Purified fractions from EMD suppressed proliferation of GE-1 and SCC-25. LC-MS/MS revealed that ameloblastin in EMD is the component responsible for inhibiting epithelial cell proliferation. The inhibitory effect of ameloblastin on the proliferation of GE-1 and SCC-25 was confirmed using recombinant protein. Conclusion: The inhibitory effects of EMD on epithelial cell proliferation are caused by the biological activities of ameloblastin, which suggests that ameloblastin is involved in regulating epithelial downgrowth in periodontal tissues.
引用
收藏
页码:49 / 55
页数:7
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