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PGE2 inhibits MMP expression by suppressing MKK4–JNK MAP kinase–c‐JUN pathway via EP4 in human articular chondrocytes
Author(s) -
Nishitani Kohei,
Ito Hiromu,
Hiramitsu Teruko,
Tsutsumi Ryosuke,
Tanida Shimei,
Kitaori Toshiyuki,
Yoshitomi Hiroyuki,
Kobayashi Masahiko,
Nakamura Takashi
Publication year - 2009
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.22421
Subject(s) - prostaglandin e2 , phosphorylation , gene knockdown , kinase , mapk/erk pathway , chemistry , matrix metalloproteinase , microbiology and biotechnology , c jun , prostaglandin e2 receptor , endocrinology , agonist , biology , receptor , biochemistry , transcription factor , gene , apoptosis
Prostaglandin E2 (PGE2) is one of pro‐inflammatory mediators. PGE2 maintains the homeostasis of many organs including articular cartilage, and a previous report showed that continuous inhibition of PGE2 accelerates the progression of osteoarthritis (OA). While PGE2 inhibits matrix metalloprotease (MMP) expression in several types of cells, little is known on direct effects of PGE2 on MMP expression in articular chondrocytes. The objective of this study was to investigate direct effects of PGE2 on IL‐1β‐induced MMP‐1 and MMP‐13 expression and the intracellular signaling in articular chondrocytes. PGE2 showed inhibitory effects on IL‐1β‐induced MMP‐1 and MMP‐13 expression demonstrated by immunoblotting both in OA and normal chondrocytes, which was further confirmed by enzyme‐linked immunosorbent assay and immunohistochemistry of explant cultures of articular cartilages. An EP4 agonist, ONO‐AE1‐329, mimicked the inhibitory effect of PGE2, while an EP4 antagonist, ONO‐AE3‐208, blocked the effects. PGE2 suppressed the phosphorylation of JNK and ERK MAP kinases, but only knockdown of JNK by specific siRNA mimicked the effect of PGE2. PGE2 further inhibited the phosphorylation of MKK4 without suppression of MKK7 phosphorylation, and of c‐JUN to decrease expression levels of MMP‐1 and MMP‐13. These results demonstrate that PGE2 inhibits IL‐1β‐induced MMP‐1 and MMP‐13 productions via EP4 by suppressing MKK4–JNK MAP kinase–c‐JUN pathway. J. Cell. Biochem. 109: 425–433, 2010. © 2009 Wiley‐Liss, Inc.

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