Dexamethasone inhibits basic fibroblast growth factor-stimulated gastric epithelial cell proliferation

被引：41

作者：

Luo, Jiing-Chyuan ^{[2
,3
]}

Lin, Hsiao-Yi ^{[3
,4
]}

Lu, Ching-Liang ^{[2
,3
]}

Wang, Lung-Yao ^{[2
]}

Chang, Full-Young ^{[2
,3
]}

Lin, Han-Chieh ^{[2
,3
]}

Huang, Yi-Chen ^{[2
]}

Ng, Ka-Man ^{[2
,3
]}

Chi, Chin-Wen ^{[1
,5
]}

Lee, Shou-Don ^{[2
,3
]}

机构：

[1] Taipei Vet Gen Hosp, Dept Med Res & Educ, Taipei 11217, Taiwan

[2] Taipei Vet Gen Hosp, Dept Med, Div Gastroenterol, Taipei 11217, Taiwan

[3] Natl Yang Ming Univ, Sch Med, Dept Med, Taipei 112, Taiwan

[4] Taipei Vet Gen Hosp, Dept Med, Div Rheumatol Allergy & Immunol, Taipei 11217, Taiwan

[5] Natl Yang Ming Univ, Sch Med, Inst Pharmacol, Taipei 112, Taiwan

来源：

BIOCHEMICAL PHARMACOLOGY | 2008年 / 76卷 / 07期

关键词：

bFGF; COX; dexamethasone; ERK1/ERK2; proliferation;

D O I：

10.1016/j.bcp.2008.07.010

中图分类号：

R9 [药学];

学科分类号：

1007 [药学];

摘要：

Basic fibroblast growth factor (bFGF) is essential for gastric ulcer healing, whereas glucocorticoids delay gastric ulcer healing. We found that dexamethasone inhibited bFGF-stimulated rat gastric epithelial RGM-1 cells proliferation and attempted to elucidate the possible mechanistic pathway. Flowcytometry was used to determine cell proliferation. Western blot and RT-PCR were performed to evaluate changes in signaling pathways. Results showed that bFGF significantly increased mRNA expression of FGF receptor (FGFR)l and FGFR2 at 10 min and increased expression of phosphorylated extracellular signal-regulated kinase (pERK1/pERK2) but not phosphorylated p38 mitogen-activated protein kinase (MAPK) or phosphorylated phosphatidylinositol 3-kinase (PI3K) within 30 min. This was followed by an increase of cyclooxygenase (COX)-2 mRNA and protein expression at 30 and 240 min, respectively. Mitogen-activated protein kinase kinase (MEK) inhibitor-PD98059 (10(-5) M) markedly suppressed bFGF-stimulated COX-2 expression and cell proliferation, but neither p38 MAPK inhibitor-SB203580 nor PI3K inhibitor-Wortmannin had any effect. Dexamethasone (10(-6) M) substantially reduced bFGF-stimulated ERK activation at 10 min, COX-2 mRNA and protein expression at 30 and 240 min, respectively, and prostaglandin E-2 synthesis at 8 h. Dexamethasone (10-6 M) also significantly decreased mRNA expression of FGFR1 and FGFR2 at basal and bFGF-stimulated conditions at 10 min. This study indicated that bFGF-stimulated gastric epithelial RGM-1 cells proliferation via up-regulating FGFR1 and FGFR2, activating ERK1/ERK2 signal transduction pathway and COX-2 pathway. Dexamethasone significantly suppresses bFGF-stimulated RGM-1 cells proliferation in part via down-regulation of FGFR1/FGFR2, then decreasing bFGF-stimulated activation of ERK1/ERK2, followed by inhibition of COX-2 activation, and finally DNA synthesis. (c) 2008 Elsevier Inc. All rights reserved.

引用

页码：841 / 849

页数：9

共 27 条

[1]

Biological roles of fibroblast growth factor-2 [J].