Volume 110, Issue 2 pp. 130-136

Physiologic levels of Epidermal Growth Factor in saliva stimulate cell migration of an oral epithelial cell line, HO-1-N-1

Mitsuhiro Ohshima

Mitsuhiro Ohshima

Department of Biochemistry, Nihon University School of Dentistry, Kanda-Surugadai, Chiyoda-ku, Tokyo, Japan

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Masashi Sato

Masashi Sato

Department of Biochemistry, Nihon University School of Dentistry, Kanda-Surugadai, Chiyoda-ku, Tokyo, Japan

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Masako Ishikawa

Masako Ishikawa

Department of Biochemistry, Nihon University School of Dentistry, Kanda-Surugadai, Chiyoda-ku, Tokyo, Japan

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Masao Maeno

Masao Maeno

Department of Biochemistry, Nihon University School of Dentistry, Kanda-Surugadai, Chiyoda-ku, Tokyo, Japan

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Kichibee Otsuka

Kichibee Otsuka

Department of Biochemistry, Nihon University School of Dentistry, Kanda-Surugadai, Chiyoda-ku, Tokyo, Japan

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First published: 30 April 2002
Citations: 39
Mitsuhiro Ohshima, Department of Biochemistry, Nihon University School of Dentistry, 1-8-13 Kanda-Surugadai, Chiyoda-ku, Tokyo 101–8310, Japan
Telefax: +81–3–32198334
E-mail: [email protected]

Abstract

An oral epithelial cell line derived from buccal mucosa squamous cell carcinoma, HO-1-N-1, was used to elucidate the role of epidermal growth factor (EGF) in saliva on wound healing of the oral mucosa. The effects of EGF on DNA synthesis, and cell migration was studied and the related signal transduction pathways examined. DNA synthesis by HO-1-N-1 cells was stimulated dose-dependently by 1–10 ng ml−1 EGF, but significantly inhibited by addition of a PI3-K inhibitor (wortmannin), a p38 MAPK inhibitor (SB203580) or an MEKs inhibitor (PD98059). Cell migration was also accelerated by addition of 1–10 ng ml−1 EGF; however, the migration rate was decreased to 30% by adding PD98059, to 40% by adding a tyrosine kinase inhibitor (herbimycin A), and to 60% by adding wortmannin or dexamethasone. These results indicate that the physiologic concentration of EGF in saliva may stimulate proliferation and migration of oral epithelial cells for wound healing, when the oral mucosa has been injured. Furthermore, this study revealed that EGF-stimulated signal transduction pathways for epithelial cell proliferation and cell migration are different.

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