12-oxo-phytodienoic acid, a plant-derived oxylipin, attenuates lipopolysaccharide-induced inflammation in microglia

被引:20
作者
Taki-Nakano, Nozomi [1 ,2 ]
Kotera, Jun [2 ]
Ohta, Hiroyuki [1 ,3 ]
机构
[1] Tokyo Inst Technol, Grad Sch Biosci & Biotechnol, Midori Ku, 4259-B-65 Nagatsuta Cho, Yokohama, Kanagawa 2268501, Japan
[2] Mitsubishi Tanabe Pharma Corp, Sohyaku Innovat Res Div, Adv Drug Res Labs, 2-2-50 Kawagishi, Toda, Saitama 3358505, Japan
[3] Tokyo Inst Technol, Sch Life Sci & Technol, Midori Ku, 4259-B-65 Nagatsuta Cho, Yokohama, Kanagawa 2268501, Japan
关键词
Plant oxylipins; Jasmonates; OPDA; Anti-inflammatory activity; Microglia; NF-KAPPA-B; CYTOKINE UP-REGULATION; OXIDATIVE STRESS; SIGNAL-TRANSDUCTION; P38-ALPHA MAPK; NITRIC-OXIDE; JASMONATE; J(2); MECHANISMS; EXPRESSION;
D O I
10.1016/j.bbrc.2016.04.060
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Jasmonates are plant lipid-derived oxylipins that act as key signaling compounds in plant immunity, germination, and development. Although some physiological activities of natural jasmonates in mammalian cells have been investigated, their anti-inflammatory actions in mammalian cells remain unclear. Here, we investigated whether jasmonates protect mouse microglial MG5 cells against lipopolysaccharide (LPS)-induced inflammation. Among the jasmonates tested, only 12-oxo-phytodienoic acid (OPDA) suppressed LPS-induced expression of the typical inflammatory cytokines interleukin-6 and tumor necrosis factor alpha. In addition, only OPDA reduced LPS-induced nitric oxide production through a decrease in the level of inducible nitric oxide synthase. Further mechanistic studies showed that OPDA suppressed neuroinflammation by inhibiting nuclear factor kappa B and p38 mitogen-activated protein kinase signaling in LPS-activated MG5 cells. In addition, OPDA induced expression of suppressor of cytokine signaling-1 (SOCS-1), a negative regulator of inflammation, in MG5 cells. Finally, we found that the nuclear factor erythroid 2-related factor 2 signaling cascade induced by OPDA is not involved in the anti-inflammatory effects of OPDA. These results demonstrate that OPDA inhibited LPS-induced cell inflammation in mouse microglial cells via multiple pathways, including suppression of nuclear factor kappa B, inhibition of p38, and activation of SOCS-1 signaling. (C) 2016 The Authors. Published by Elsevier Inc.
引用
收藏
页码:1288 / 1294
页数:7
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