Volume 24, Issue 4 pp. 501-508

Thrombin-stimulated proliferation is mediated by endothelin-1 in cultured rat gingival fibroblasts

Nozomi Ohuchi

Corresponding Author

Nozomi Ohuchi

Laboratory of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Josai International University, 1 Gumyo, Togane, Chiba 283-8555, Japan

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Kazuhiko Hayashi

Kazuhiko Hayashi

Nihon University School of Dentistry at Matsudo, Matsudo, Chiba 271-8587, Japan

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Keishi Iwamoto

Keishi Iwamoto

Department of Pharmacology, Toho University School of Pharmaceutical Sciences, Miyama, Funabashi, Chiba 274-8510, Japan

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Katsuo Koike

Katsuo Koike

Department of Pharmacology, Toho University School of Pharmaceutical Sciences, Miyama, Funabashi, Chiba 274-8510, Japan

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Yasuo Kizawa

Yasuo Kizawa

Department of Physiology and Anatomy, Nihon University College of Pharmacy, Narashinodai, Funabashi, Chiba 274-8555, Japan

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Michiyoshi Nukaga

Michiyoshi Nukaga

Laboratory of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Josai International University, 1 Gumyo, Togane, Chiba 283-8555, Japan

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Tomohito Kakegawa

Tomohito Kakegawa

Laboratory of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Josai International University, 1 Gumyo, Togane, Chiba 283-8555, Japan

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Hajime Murakami

Hajime Murakami

Department of Pharmacology, Toho University School of Pharmaceutical Sciences, Miyama, Funabashi, Chiba 274-8510, Japan

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First published: 06 July 2010
Citations: 11

Abstract

Endothelin-1 (ET-1) appears to be involved in drug-induced proliferation of gingival fibroblasts. Thrombin induces proliferation of human gingival fibroblasts via protease-activated receptor 1 (PAR1). In this study, using cultured rat gingival fibroblasts, we investigated whether thrombin-induced proliferation of gingival fibroblasts is mediated by ET-1. Thrombin-induced proliferation (0.05–2.5 U/mL). Proliferation was also induced by a PAR1-specific agonist (TFLLR-NH2, 0.1–30 μm), but not by a PAR2-specific agonist (SLIGRL-NH2). Thrombin (2.5 U/mL) induced an increase in immunoreactive ET-1 expression, which was inhibited by cycloheximide (10 μg/mL), and an increase in preproET-1 mRNA expression, as assessed by reverse transcription polymerase chain reaction. TFLLR-NH2 increased ET-1 release into the culture medium in both a concentration (0.01–10 μm)- and time (6–24 h)-dependent manner, as assessed by solid phase sandwich enzyme-linked immunosorbent assay. The thrombin (2.5 U/mL)-induced proliferation was inhibited by a PAR1-selective inhibitor, SCH79797 (0.1 μm) and an ETA antagonist, BQ-123 (1 μm), but not by an ETB antagonist, BQ-788 (1 μm). These findings suggest that thrombin, acting via PAR1, induced proliferation of cultured rat gingival fibroblasts that was mediated by ET-1 acting via ETA.

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