Trans-10, cis-12-conjugated linoleic acid attenuates tumor necrosis factor-α production by lipopolysaccharide-stimulated porcine peripheral blood mononuclear cells through induction of interleukin-10

被引:10
作者
Kim, Keun-Hwa [1 ]
Kim, Dong-In [1 ]
Kim, Soo-Hyun [1 ]
Jung, Eui-Man [2 ,3 ]
Kang, Ji-Houn [1 ]
Jeung, Eui-Bae [2 ,3 ]
Yang, Mhan-Pyo [1 ]
机构
[1] Chungbuk Natl Univ, Dept Vet Med, Coll Vet Med, Lab Vet Internal Med, Cheongju 361763, Chungbuk, South Korea
[2] Chungbuk Natl Univ, Dept Vet Med, Coll Vet Med, Lab Vet Biochem & Mol Biol, Cheongju 361763, Chungbuk, South Korea
[3] Chungbuk Natl Univ, Vet Med Res Inst, Cheongju 361763, Chungbuk, South Korea
关键词
Trans-10; cis-12-conjugated linoleic acid; Lipopolysaccharide; Tumor necrosis factor-alpha; Interleukin-10; Peripheral blood mononuclear cells; NF-KAPPA-B; EXPRESSION; IL-10; PHAGOCYTOSIS; MACROPHAGES; GENE;
D O I
10.1016/j.cyto.2011.06.019
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
Conjugated linoleic acid (CLA) can stimulate or inhibit immune cell function, and among CLA isomers, trans-10, Cis-12 (t10c12)-CLA was shown to participate in the modulation of pro- or anti-inflammatory cytokine secretion. The objective of this study was to examine the effect of t10c12-CLA on tumor necrosis factor (TNF)-alpha production by lipopolysaccharide (LPS)-stimulated porcine peripheral blood mononuclear cells (PBMCs). In addition, we determined whether these effects were associated with the induction of interleukin (IL)-10. Treatment of LPS-unstimulated porcine PBMCs with t10c12-CLA increased both TNF-alpha expression and IL-10 production. However, treatment of LPS-stimulated porcine PBMCs with t10c12-CLA suppressed TNF-alpha production and increased the levels of IL-10. Furthermore, treatment of LPS-stimulated porcine PBMCs with IL-10 suppressed the production of TNF-alpha. The effects of t10c12-CLA on TNF-alpha expression by both LPS-naive and LPS-stimulated PBMCs were inhibited by IL-10 treatment. The suppressive effects of t10c12-CLA on TNF-alpha production by LPS-stimulated porcine PBMCs were inhibited by an anti-IL-10 polyclonal antibody. These findings suggest that t10c12-CLA has an immunostimulatory effect on porcine PBMCs mediated via the up-regulation of TNF-alpha production, and an anti-inflammatory effect in LPS-stimulated PBMCs mediated via the down-regulation of TNE-alpha production, and that both is likely to be associated with the induction of IL-10. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:224 / 230
页数:7
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