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The anacardic 6-pentadecyl salicylic acid induces macrophage activation via the phosphorylation of ERK1/2, JNK, P38 kinases and NF-κB
被引:30
|作者:
Gnanaprakasam, J. N. Rashida
[1
]
Estrada-Muniz, Elizabet
[1
]
Vega, Libia
[1
]
机构:
[1] Natl Polytech Inst, Ctr Res & Adv Studies, Dept Toxicol, Mexico City 07360, DF, Mexico
关键词:
6-pentadecyl salicylic acid;
MAP kinases;
Macrophages;
Immuno-modulation;
STABILIZING ANTINEOPLASTIC AGENT;
NITRIC-OXIDE;
MAP KINASES;
IMMUNOSTIMULATORY ACTIVITY;
SIGNALING PATHWAY;
CELLS;
PROLIFERATION;
TAXOL;
LIPOPOLYSACCHARIDE;
POLYSACCHARIDES;
D O I:
10.1016/j.intimp.2015.08.038
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Amphipterygium adstringens is a plant traditionally used to treat gingivitis, gastric ulcer and even gastric cancer but the mechanism involved in the regulation of the immune response is not elucidated yet. The 6-pentadecylsalicylic acid (6SA) is the main anacardic acid found in A. adstringens. In order to evaluate the immune-modulatory abilities of 6SA, we used mouse splenocytes and determined the phosphorylation of the transcription factor NF-kappa B and MAP kinases ERK1/2, JNK and p38 in helper and cytotoxic T cells, natural killer (NK) cells and F4/80(+) macrophages. Treatment with 6SA was not cytotoxic as measured by both trypan blue exclusion and tetrazolium salts (MU) tests. Additionally, 6SA did not alter the proportion of helper and cytotoxic T lymphocytes, NK cells or macrophages. Moreover, 6SA treatment significantly increased the phosphorylation of ERK1/2, JNK, P38 and NF-kappa B mainly in macrophages. In this cells (peritoneal macrophages), treatment with 6SA increased the secretion of nitric oxide (NO), interleukin (IL)-6 and tumour necrosis factor (TNF)-alpha and decreased the secretion of IL-4 and IL-10 depending on MARK and NF-kappa B phosphorylation. In addition, 6SA increased the migration and phagocytic activity of macrophages also depending on the phosphorylation of different kinases. These data suggest that 6SA induces the classical activation pathway in macrophages via the phosphorylation of MAP kinases and NF-kappa B thus activating the adaptive immune system. (C) 2015 Elsevier B.V. All rights reserved.
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页码:808 / 817
页数:10
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