Effect of Vitronectin Bound to Insulin-Like Growth Factor-I and Insulin-Like Growth Factor Binding Protein-3 on Porcine Enamel Organ-Derived Epithelial Cells

The aim of this paper was to determine whether the interaction between IGF, IGFBP, and VN modulates the functions of porcine EOE cells. Enamel organs from 6-month-old porcine third molars were dissociated into single epithelial cells and subcultured on culture dishes pretreated with VN, IGF-I, and I...

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Main Authors: Yoshinori Shinohara, Shuhei Tsuchiya, Kazuo Hatae, Masaki J. Honda
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:International Journal of Dentistry
Online Access:http://dx.doi.org/10.1155/2012/386282
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spelling doaj-e9ccccc9d4274bc58cc5ad3278a33bda2020-11-24T22:36:21ZengHindawi LimitedInternational Journal of Dentistry1687-87281687-87362012-01-01201210.1155/2012/386282386282Effect of Vitronectin Bound to Insulin-Like Growth Factor-I and Insulin-Like Growth Factor Binding Protein-3 on Porcine Enamel Organ-Derived Epithelial CellsYoshinori Shinohara0Shuhei Tsuchiya1Kazuo Hatae2Masaki J. Honda3Division of Stem Cell Engineering, Institute of Medical Science, The University of Tokyo, Minato-ku, Tokyo 108-8639, JapanDivision of Stem Cell Engineering, Institute of Medical Science, The University of Tokyo, Minato-ku, Tokyo 108-8639, JapanCOREFRONT Corporation, Shinjuku-ku, 160-0008 Tokyo, JapanDivision of Stem Cell Engineering, Institute of Medical Science, The University of Tokyo, Minato-ku, Tokyo 108-8639, JapanThe aim of this paper was to determine whether the interaction between IGF, IGFBP, and VN modulates the functions of porcine EOE cells. Enamel organs from 6-month-old porcine third molars were dissociated into single epithelial cells and subcultured on culture dishes pretreated with VN, IGF-I, and IGFBP-3 (IGF-IGFBP-VN complex). The subcultured EOE cells retained their capacity for ameloblast-related gene expression, as shown by semiquantitative reverse transcription-polymerase chain reaction. Amelogenin expression was detected in the subcultured EOE cells by immunostaining. The subcultured EOE cells were then seeded onto collagen sponge scaffolds in combination with fresh dental mesenchymal cells and transplanted into athymic rats. After 4 weeks, enamel-dentin-like complex structures were present in the implanted constructs. These results show that EOE cells cultured on IGF-IGFBP-VN complex differentiated into ameloblasts-like cells that were able to secrete amelogenin proteins and form enamel-like tissues in vivo. Functional assays demonstrated that the IGF/IGFBP/VN complex significantly enhanced porcine EOE cell proliferation and tissue forming capacity for enamel. This is the first study to demonstrate a functional role of the IGF-IGFBP-VN complex in EOE cells. This application of the subculturing technique provides a foundation for further tooth-tissue engineering and for improving our understanding of ameloblast biology.http://dx.doi.org/10.1155/2012/386282
collection DOAJ
language English
format Article
sources DOAJ
author Yoshinori Shinohara
Shuhei Tsuchiya
Kazuo Hatae
Masaki J. Honda
spellingShingle Yoshinori Shinohara
Shuhei Tsuchiya
Kazuo Hatae
Masaki J. Honda
Effect of Vitronectin Bound to Insulin-Like Growth Factor-I and Insulin-Like Growth Factor Binding Protein-3 on Porcine Enamel Organ-Derived Epithelial Cells
International Journal of Dentistry
author_facet Yoshinori Shinohara
Shuhei Tsuchiya
Kazuo Hatae
Masaki J. Honda
author_sort Yoshinori Shinohara
title Effect of Vitronectin Bound to Insulin-Like Growth Factor-I and Insulin-Like Growth Factor Binding Protein-3 on Porcine Enamel Organ-Derived Epithelial Cells
title_short Effect of Vitronectin Bound to Insulin-Like Growth Factor-I and Insulin-Like Growth Factor Binding Protein-3 on Porcine Enamel Organ-Derived Epithelial Cells
title_full Effect of Vitronectin Bound to Insulin-Like Growth Factor-I and Insulin-Like Growth Factor Binding Protein-3 on Porcine Enamel Organ-Derived Epithelial Cells
title_fullStr Effect of Vitronectin Bound to Insulin-Like Growth Factor-I and Insulin-Like Growth Factor Binding Protein-3 on Porcine Enamel Organ-Derived Epithelial Cells
title_full_unstemmed Effect of Vitronectin Bound to Insulin-Like Growth Factor-I and Insulin-Like Growth Factor Binding Protein-3 on Porcine Enamel Organ-Derived Epithelial Cells
title_sort effect of vitronectin bound to insulin-like growth factor-i and insulin-like growth factor binding protein-3 on porcine enamel organ-derived epithelial cells
publisher Hindawi Limited
series International Journal of Dentistry
issn 1687-8728
1687-8736
publishDate 2012-01-01
description The aim of this paper was to determine whether the interaction between IGF, IGFBP, and VN modulates the functions of porcine EOE cells. Enamel organs from 6-month-old porcine third molars were dissociated into single epithelial cells and subcultured on culture dishes pretreated with VN, IGF-I, and IGFBP-3 (IGF-IGFBP-VN complex). The subcultured EOE cells retained their capacity for ameloblast-related gene expression, as shown by semiquantitative reverse transcription-polymerase chain reaction. Amelogenin expression was detected in the subcultured EOE cells by immunostaining. The subcultured EOE cells were then seeded onto collagen sponge scaffolds in combination with fresh dental mesenchymal cells and transplanted into athymic rats. After 4 weeks, enamel-dentin-like complex structures were present in the implanted constructs. These results show that EOE cells cultured on IGF-IGFBP-VN complex differentiated into ameloblasts-like cells that were able to secrete amelogenin proteins and form enamel-like tissues in vivo. Functional assays demonstrated that the IGF/IGFBP/VN complex significantly enhanced porcine EOE cell proliferation and tissue forming capacity for enamel. This is the first study to demonstrate a functional role of the IGF-IGFBP-VN complex in EOE cells. This application of the subculturing technique provides a foundation for further tooth-tissue engineering and for improving our understanding of ameloblast biology.
url http://dx.doi.org/10.1155/2012/386282
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