IL-10 plays a pivotal role in anti-inflammatory effects of resveratrol in activated microglia cells

被引:156
作者
Cianciulli, Antonia [1 ]
Dragone, Teresa [1 ]
Calvello, Rosa [1 ]
Porro, Chiara [2 ]
Trotta, Teresa [2 ]
Lofrumento, Dario Domenico [3 ]
Panaro, Maria Antonietta [1 ]
机构
[1] Univ Bari, Dept Biosci Biotechnol & Biopharmaceut, I-70121 Bari, Italy
[2] Univ Foggia, Dept Clin & Expt Med, Foggia, Italy
[3] Univ Salento, Sect Human Anat, Dept Biol & Environm Sci & Technol, Lecce, Italy
关键词
Microglia; Resveratrol; IL-10; Inflammation; Neurological diseases; MACROPHAGE ACTIVATION; INFLAMMATORY RESPONSE; CYTOKINE RECEPTORS; MURINE MICROGLIA; TNF-ALPHA; INTERLEUKIN-10; MECHANISMS; MONOCYTE; RELEASE; INHIBITORS;
D O I
10.1016/j.intimp.2014.12.035
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The development of agents that can modulate microglial activation has been suggested as one potential strategy for the treatment or prevention of neurodegenerative diseases. Among these agents, resveratrol, with its anti-inflammatory action, has been described to have neuroprotective effects. In this paper we demonstrate that in LPS-stimulated microglia resveratrol pretreatment reduced, in a dose-dependent manner, pro-inflammatory cytokines IL-13, TNF-alpha and IL-6 mRNA expression and increased the release of anti-inflammatory interleukin (IL)-10. Moreover, resveratrol pretreatment up-regulated the phosphorylated forms of JAK1 and STAT3, as well as suppressor of cytokine signaling (SOCS)3 protein expression in LPS activated cells, demonstrating that the JAK-STAT signaling pathway is involved in the anti-inflammatory effect exerted by resveratrol. By supplementing the cultures with an IL-10 neutralizing antibody (IL-10NA) we obtained the opposite effect. Taken together, these data allow us to conclude that the LPS-induced pro-inflammatory response in microglial cells can be markedly reduced by resveratrol, through IL-10 dependent up-regulation of SOCS3, requiring the JAR-STAT signaling pathway. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:369 / 376
页数:8
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