Authors: Arai, Toru
Hirata, Haruhiko
Hoshino, Shigenori
Inoue, Koji
Kawase, Ichiro
Kida, Hiroshi
Kijima, Takashi
Kumagai, Toru
Osaki, Tadashi
Tachibana, Isao
Takimoto, Takayuki
Yanagita, Masahiko
Yano, Yukihiro
Yoshida, Mitsuhiro
Title: IL-10 Inhibits Transforming Growth Factor-ß-Induction of Type I Collagen mRNA Expression via Both JNK and p38 Pathways in Human Lung Fibroblasts
Language (ISO): en
Abstract: Transforming growth factor-ß (TGF-ß) is a key factor for understanding the pathogenesis of fibrotic disorders such as idiopathic pulmonary fibrosis (IPF). We have demonstrated that interleukin-10 (IL-10) suppresses TGF-ß-induced expression of type I collagen (COL1) mRNA in a human lung fibroblast cell line (WI-38). However, the inhibitory mechanism has not yet been clearly elucidated. Thus, in the current study, we investigate the effects of IL-10 blockade of TGF-ß signaling which regulates COL1 mRNA expression. In WI-38 cells, IL-10 inhibits TGF-ß-mediated phosphorylation of both, c-Jun HN2-terminal kinase (JNK) and p38, but does not suppress TGF-ß- mediated phosphorylation of Smad2 or affect TGF-ß-upregulation of Smad7 mRNA expression. In addition, SP600125 and SB203580, specific inhibitors of JNK and p38, respectively, attenuate TGF-ß-induced COL1 mRNA expression in WI-38 cells. These results suggest that IL-10 inhibits TGF-ß-induced COL1 mRNA expression via both JNK and p38 pathways but not Smad pathways in WI-38 cells. This inhibitory mechanism may provide a novel insight into therapeutic strategies for fibrotic disorders such as IPF.
Subject Headings: collagen
IL-10
JNK
Smad
TGF-ß
URI: http://hdl.handle.net/2003/25650
http://dx.doi.org/10.17877/DE290R-8281
Issue Date: 2005-08-11
Appears in Collections:Original Articles

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