Induction of distinct sets of secretory phospholipase A2 in rodents during inflammation |
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Authors: | Katsuhiko Hamaguchi Hiroshi Kuwata Kumiko Yoshihara Seiko Masuda Satoko Shimbara Sachiko Oh-ishi Makoto Murakami Ichiro Kudo |
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Affiliation: | 1. Department of Health Chemistry, School of Pharmaceutical Sciences, Showa University, 1-5-8 Hatanodai, Shinagawa, Tokyo 142-8555, Japan;2. Corporate Licensing Department, Yamanouchi Pharmaceutical Co., Ltd., 2-3-11 Nihonbashi-Honcho, Chuo, Tokyo 103-8411, Japan |
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Abstract: | ![]() Although the expression of the prototypic secretory phospholipase A2 (sPLA2), group IIA (sPLA2-IIA), is known to be up-regulated during inflammation, it remains uncertain if other sPLA2 enzymes display similar or distinct profiles of induction under pathological conditions. In this study, we investigated the expression of several sPLA2s in rodent inflammation models. In lipopolysaccharide (LPS)-treated mice, the expression of sPLA2-V, and to a lesser extent that of sPLA2-IID, -IIE, and -IIF, were increased, whereas that of sPLA2-X was rather constant, in distinct tissues. 12-O-Tetradecanoylphorbol-13-acetate (TPA)-induced mouse ear edema, in which the expression of sPLA2-IID, -IIF and -V was increased, was significantly reduced by YM-26734, a competitive sPLA2-IIA inhibitor that turned out to inhibit sPLA2-IID, -IIE, -V and -X as well. In contrast, sPLA2-IIA was dominant in carageenin-induced pleurisy in rats, where the accumulation of exudate fluids and leukocytes was significantly ameliorated by YM-26734. These results indicate that distinct sPLA2s can participate in inflammatory diseases according to tissues, animal species, and types of inflammation. |
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