Novel biological activity of ameloblastin in enamel matrix derivative

Authors

  • Sachiko KURAMITSU-FUJIMOTO Kyushu Dental University; Department of Growth Development of Functions; Division of Orofacial Functions and Orthodontics
  • Wataru ARIYOSHI Kyushu Dental University; Department of Health Promotion; Division of Infections and Molecular Biology
  • Noriko SAITO Kyushu Dental University; Department of Cariology and Periodontology; Division of Pulp Biology, Operative Dentistry and Endodontics
  • Toshinori OKINAGA Kyushu Dental University; Department of Health Promotion; Division of Infections and Molecular Biology
  • Masaharu KAMO Iwate Medical University; Department of Biochemistry; Division of Cellular Biosignal Sciences
  • Akira ISHISAKI Iwate Medical University; Department of Biochemistry; Division of Cellular Biosignal Sciences
  • Takashi TAKATA Hiroshima University; Institute of Biomedical and Health Sciences; Department of Oral and Maxillofacial Pathobiology
  • Kazunori YAMAGUCHI Kyushu Dental University; Department of Growth Development of Functions; Division of Orofacial Functions and Orthodontics
  • Tatsuji NISHIHARA Kyushu Dental University; Department of Health Promotion; Division of Infections and Molecular Biology

DOI:

https://doi.org/10.1590/1678-775720140291

Abstract

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.

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Published

2015-02-01

Issue

Section

Original Articles

How to Cite

Novel biological activity of ameloblastin in enamel matrix derivative . (2015). Journal of Applied Oral Science, 23(1), 49-55. https://doi.org/10.1590/1678-775720140291