Biochemistry and Molecular Biology

| Peer-Reviewed |

Distinct Role of Transforming Growth Factor-Beta 1 and Fibroblast Growth Factors in Human Amelobastoma Epithelial Cell Proliferation

Received: 30 January 2017    Accepted: 22 February 2017    Published: 9 March 2017
Views:       Downloads:

Share This Article

Abstract

Ameloblastoma is a locally invasive benign epithelial odontogenic tumor and its histopathological structures are similar to the enamel organ. Although various studies have investigated cell proliferation in ameloblastoma to elucidate the biological behavior and clinicopathological mechanisms, it remains poorly understood. The studies on the development of the enamel organ reports that FGF-9, -10, and TGF-β1 are strongly involved in dental epithelial cell differentiation and cell proliferation. In this study, we attempt to evaluate the effect of these growth factors on ameloblastoma cells. Both collagen-coated and normal plastic cell culture plate cell growth curves were steeper in the presence of growth supplement than in the absence of growth supplement. The presence of TGF-β1 at each dose (1 to 10 ng/ml), however, suppressed the number of cells cultured on the collagen-coated plate but made no significant difference on the normal plastic plate. The number of cells was increased in the presence of FGF-10 at 100 ng/ml, but not in the presence of FGF-9 after 48 h culture. These results suggest that FGF-10 and TGF-β1 play distinct roles in the cell proliferation of human ameloblastoma cells.

DOI 10.11648/j.bmb.20170201.11
Published in Biochemistry and Molecular Biology (Volume 2, Issue 1, January 2017)
Page(s) 1-5
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Fibroblast Growth Factor (FGF), Transforming Growth Factor-Beta 1 (TGF-β1), Dental Epithelial Cell, Cell Proliferation

References
[1] Gardner DG, Heikinheimo K, Shear M, Philipsen HP, Coleman H. “Ameloblastomas”, Pathology and Genetics of Head and Neck Tumours, World Health Organization Classification of Tumours. Barnes L, Eveson JW, Reichart P, Sidransky D edi, IARC Press, 2005, pp296-300.
[2] Li CY, Prochazka J, Goodwin AF, Klein OD. Fibroblast growth factor signaling in mammalian tooth development. Odontology. 2014, 102(1):1-13.
[3] Kettunen P, Karavanova I, Thesleff I. Responsiveness of developing dental tissues to fibroblast growth factors: expression of splicing alternatives of FGFR1, -2, -3, and of FGFR4; and stimulation of cell proliferation by FGF-2, -4, -8, and -9. Dev Genet. 1998, 22:374–85.
[4] Kettunen P, Thesleff I. Expression and function of FGFs-4, -8, and -9 suggest functional redundancy and repetitive use as epithelial signals during tooth morphogenesis. Dev Dyn. 1998, 211:256–68.
[5] Kettunen P, Laurikkala J, Itäranta P, Vainio S, Itoh N, Thesleff I. Associations of FGF-3 and FGF-10 with signaling networks regulating tooth morphogenesis. Dev Dyn. 2000, 219(3):322-32.
[6] Kurosaka H, Islam MN, Kuremoto K, Hayano S, Nakamura M, Kawanabe N, Yanagita T, Rice DP, Harada H, Taniuchi I, Yamashiro T. Core binding factor beta functions in the maintenance of stem cells and orchestrates continuous proliferation and differentiation in mouse incisors. Stem Cells. 2011, 29(11):1792-803.
[7] Kawano S, Saito M, Handa K, Morotomi T, Toyono T, Seta Y, Nakamura N, Uchida T, Toyoshima K, Ohishi M, Harada H. Characterization of dental epithelial progenitor cells derived from cervical-loop epithelium in a rat lower incisor. J Dent Res. 2004, 83(2):129-33.
[8] Tai YY, Chen RS, Lin Y, Ling TY, Chen MH. FGF-9 accelerates epithelial invagination for ectodermal organogenesis in real time bioengineered organ manipulation. Cell Commun Signal. 2012, 10(1):34.
[9] Miyazono K, Kusanagi K, Inoue H. Divergence and convergence of TGF-beta/BMP signaling. J Cell Physiol. 2001, 187(3):265-76.
[10] Sporn MB, Roberts AB. TGF-beta: problems and prospects. Cell Regul. 1990, 1(12):875-82.
[11] D’Souza RN, Happonen RP, Ritter NM, Butler WT. Temporal and spatial patterns of transforming growth factor-beta 1 expression in developing rat molars. Arch Oral Biol. 1990, 35(12):957-65.
[12] Haruyama N, Thyagarajan T, Skobe Z, Wright JT, Septier D, Sreenath TL, Goldberg M, Kulkarni AB. Overexpression of transforming growth factor-beta1 in teeth results in detachment of ameloblasts and enamel defects. Eur J Oral Sci. 2006, 114 Suppl 1:30-4; discussion 39-41, 379.
[13] Klopcic B, Maass T, Meyer E, Lehr HA, Metzger D, Chambon P, Mann A, Blessing M. TGF-beta superfamily signaling is essential for tooth and hair morphogenesis and differentiation. Eur J Cell Biol. 2007, 86(11-12):781-99.
[14] Gao Y, Li D, Han T, Sun Y, Zhang J. TGF-beta1 and TGFBR1 are expressed in ameloblasts and promote MMP20 expression. Anat Rec (Hoboken). 2009, 292(6):885-90.
[15] Tsuchiya M, Sharma R, Tye CE, Sugiyama T, Bartlett JD. Transforming growth factor-beta1 expression is up-regulated in maturation-stage enamel organ and may induce ameloblast apoptosis. Eur J Oral Sci. 2009, 117(2):105-12.
[16] Hatakeyama S, Mizusawa N, Tsutsumi R, Yoshimoto K, Mizuki H, Yasumoto S, Sato S, Takeda Y. Establishment of human dental epithelial cell lines expressing ameloblastin and enamelin by transfection of hTERT and cdk4 cDNAs. J Oral Pathol Med. 2011, 40(3):227-34.
[17] Matsuda Y, Hatakeyama Y, Nakashima K, Kamogashira N, Hatakeyama J, Tamaoki S, Sawa Y, Ishikawa H. Effect of a chemically synthesized leucine-rich amelogenin peptide (csLRAP) on chondrogenic and osteogenic cells. J Hard Tisse Biology. 2017, 26(1):51-60.
[18] Tabata MJ, Matsumura T, Fujii T, Abe M, Kurisu K. Fibronectin accelerates the growth and differentiation of ameloblast lineage cells in vitro. J Histochem Cytochem. 2003, 51(12):1673-9.
[19] Kim J, Yook JI. Immunohistochemical study on proliferating cell nuclear antigen expression in ameloblastomas. Eur J Cancer B Oral Oncol. 1994, 30 B(2):126-31.
[20] Meer S, Galpin JS, Altini M, Coleman H, Ali H. Proliferating cell nuclear antigen and Ki67 immunoreactivity in ameloblastomas. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2003, 95(2):213-21.
[21] Amaral FR, Mateus GC, Bonisson LA, Andrade BA, Mesquita RA, Horta MC, Marigo HA. Cell proliferation and apoptosis in ameloblastomas and keratocystic odontogenic tumors Braz Dent J. 2012, 23(2):91-96.
[22] Harada H, Mitsuyasu T, Nakamura N, Higuchi Y, Toyoshima K, Taniguchi A, Yasumoto S. Establishment of ameloblastoma cell line, AM-1. J Oral Pathol Med. 1998, 27(5):207-12.
[23] Nakao Y, Mitsuyasu T, Kawano S, Nakamura N, Kanda S, Nakamura S. Fibroblast growth factors 7 and 10 are involved in ameloblastoma proliferation via the mitogen-activated protein kinase pathway. Int J Oncol. 2013, 43(5):1377-84.
[24] Hatakeyama Y, Hatakeyama J, Takahashi A, Oka K, Tsuruga E, Inai T, Sawa Y. The effect of valproic acid on mesenchymal pluripotent cell proliferation and differentiation in extracellular matrices. Drug Target Insights. 2011, 5:1-9.
[25] Heikinheimo K, Jee KJ, Niini T, Aalto Y, Happonen RP, Leivo I, Knuutila S. Gene expression profiling of ameloblastoma and human tooth germ by means of a cDNA microarray. J Dent Res. 2002, 81(8):525-30.
[26] Yan Z, Chen G, Yang Y, Sun L, Jiang Z, Feng L, Yu M, Guo W, Tian W. Expression and roles of syndecan-4 in dental epithelial cell differentiation. Int J Mol Med. 2014, 34(5):1301-8.
[27] Ornitz DM, Itoh N. The fibroblast growth factor signaling pathway. Wiley Interdiscip Rev Dev Biol. 2015, 4(3):215-66.
Cite This Article
  • APA Style

    Yuko Matsuda, Naoko Kamogashira, Yuji Hatakeyama, Toshinari Mikami, Kazuki Nakashima, et al. (2017). Distinct Role of Transforming Growth Factor-Beta 1 and Fibroblast Growth Factors in Human Amelobastoma Epithelial Cell Proliferation. Biochemistry and Molecular Biology, 2(1), 1-5. https://doi.org/10.11648/j.bmb.20170201.11

    Copy | Download

    ACS Style

    Yuko Matsuda; Naoko Kamogashira; Yuji Hatakeyama; Toshinari Mikami; Kazuki Nakashima, et al. Distinct Role of Transforming Growth Factor-Beta 1 and Fibroblast Growth Factors in Human Amelobastoma Epithelial Cell Proliferation. Biochem. Mol. Biol. 2017, 2(1), 1-5. doi: 10.11648/j.bmb.20170201.11

    Copy | Download

    AMA Style

    Yuko Matsuda, Naoko Kamogashira, Yuji Hatakeyama, Toshinari Mikami, Kazuki Nakashima, et al. Distinct Role of Transforming Growth Factor-Beta 1 and Fibroblast Growth Factors in Human Amelobastoma Epithelial Cell Proliferation. Biochem Mol Biol. 2017;2(1):1-5. doi: 10.11648/j.bmb.20170201.11

    Copy | Download

  • @article{10.11648/j.bmb.20170201.11,
      author = {Yuko Matsuda and Naoko Kamogashira and Yuji Hatakeyama and Toshinari Mikami and Kazuki Nakashima and Junko Hatakeyama and Sachio Tamaoki and Yoshihiko Sawa and Hiroyuki Ishikawa},
      title = {Distinct Role of Transforming Growth Factor-Beta 1 and Fibroblast Growth Factors in Human Amelobastoma Epithelial Cell Proliferation},
      journal = {Biochemistry and Molecular Biology},
      volume = {2},
      number = {1},
      pages = {1-5},
      doi = {10.11648/j.bmb.20170201.11},
      url = {https://doi.org/10.11648/j.bmb.20170201.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.bmb.20170201.11},
      abstract = {Ameloblastoma is a locally invasive benign epithelial odontogenic tumor and its histopathological structures are similar to the enamel organ. Although various studies have investigated cell proliferation in ameloblastoma to elucidate the biological behavior and clinicopathological mechanisms, it remains poorly understood. The studies on the development of the enamel organ reports that FGF-9, -10, and TGF-β1 are strongly involved in dental epithelial cell differentiation and cell proliferation. In this study, we attempt to evaluate the effect of these growth factors on ameloblastoma cells. Both collagen-coated and normal plastic cell culture plate cell growth curves were steeper in the presence of growth supplement than in the absence of growth supplement. The presence of TGF-β1 at each dose (1 to 10 ng/ml), however, suppressed the number of cells cultured on the collagen-coated plate but made no significant difference on the normal plastic plate. The number of cells was increased in the presence of FGF-10 at 100 ng/ml, but not in the presence of FGF-9 after 48 h culture. These results suggest that FGF-10 and TGF-β1 play distinct roles in the cell proliferation of human ameloblastoma cells.},
     year = {2017}
    }
    

    Copy | Download

  • TY  - JOUR
    T1  - Distinct Role of Transforming Growth Factor-Beta 1 and Fibroblast Growth Factors in Human Amelobastoma Epithelial Cell Proliferation
    AU  - Yuko Matsuda
    AU  - Naoko Kamogashira
    AU  - Yuji Hatakeyama
    AU  - Toshinari Mikami
    AU  - Kazuki Nakashima
    AU  - Junko Hatakeyama
    AU  - Sachio Tamaoki
    AU  - Yoshihiko Sawa
    AU  - Hiroyuki Ishikawa
    Y1  - 2017/03/09
    PY  - 2017
    N1  - https://doi.org/10.11648/j.bmb.20170201.11
    DO  - 10.11648/j.bmb.20170201.11
    T2  - Biochemistry and Molecular Biology
    JF  - Biochemistry and Molecular Biology
    JO  - Biochemistry and Molecular Biology
    SP  - 1
    EP  - 5
    PB  - Science Publishing Group
    SN  - 2575-5048
    UR  - https://doi.org/10.11648/j.bmb.20170201.11
    AB  - Ameloblastoma is a locally invasive benign epithelial odontogenic tumor and its histopathological structures are similar to the enamel organ. Although various studies have investigated cell proliferation in ameloblastoma to elucidate the biological behavior and clinicopathological mechanisms, it remains poorly understood. The studies on the development of the enamel organ reports that FGF-9, -10, and TGF-β1 are strongly involved in dental epithelial cell differentiation and cell proliferation. In this study, we attempt to evaluate the effect of these growth factors on ameloblastoma cells. Both collagen-coated and normal plastic cell culture plate cell growth curves were steeper in the presence of growth supplement than in the absence of growth supplement. The presence of TGF-β1 at each dose (1 to 10 ng/ml), however, suppressed the number of cells cultured on the collagen-coated plate but made no significant difference on the normal plastic plate. The number of cells was increased in the presence of FGF-10 at 100 ng/ml, but not in the presence of FGF-9 after 48 h culture. These results suggest that FGF-10 and TGF-β1 play distinct roles in the cell proliferation of human ameloblastoma cells.
    VL  - 2
    IS  - 1
    ER  - 

    Copy | Download

Author Information
  • Section of Orthodontics, Department of Oral Growth and Development, Fukuoka Dental College, Fukuoka, Japan

  • Section of Orthodontics, Department of Oral Growth and Development, Fukuoka Dental College, Fukuoka, Japan

  • Section of Functional Structure, Department of Morphological Biology, Fukuoka Dental College, Fukuoka, Japan

  • Division of Anatomical and Cellular Pathology, Department of Pathology, Iwate Medical University, Iwate, Japan

  • Section of Orthodontics, Department of Oral Growth and Development, Fukuoka Dental College, Fukuoka, Japan

  • Section of Operative Dentistry and Endodontology, Department of Odontology, Fukuoka Dental College, Fukuoka, Japan

  • Section of Orthodontics, Department of Oral Growth and Development, Fukuoka Dental College, Fukuoka, Japan

  • Section of Functional Structure, Department of Morphological Biology, Fukuoka Dental College, Fukuoka, Japan

  • Section of Orthodontics, Department of Oral Growth and Development, Fukuoka Dental College, Fukuoka, Japan

  • Sections