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.
引用
收藏
页码:808 / 817
页数:10
相关论文
共 50 条
  • [31] Mechanical stimulation of human tendon stem/progenitor cells results in upregulation of matrix proteins, integrins and MMPs, and activation of p38 and ERK1/2 kinases
    Popov, Cvetan
    Burggraf, Martina
    Kreja, Ludwika
    Ignatius, Anita
    Schieker, Matthias
    Docheva, Denitsa
    BMC MOLECULAR BIOLOGY, 2015, 16
  • [32] Methoxychlor-induced inducible nitric oxide synthase and proinflammatory cytokines expression in macrophages via NF-κB, ERK, and p38 mitogen-activated protein kinases
    Kim, JY
    Oh, KN
    Han, EH
    Kim, DH
    Jeong, TC
    Lee, ES
    Jeong, HG
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 333 (04) : 1234 - 1240
  • [33] IL-17 Stimulates Migration of Carotid Artery Vascular Smooth Muscle Cells in an MMP-9 Dependent Manner via p38 MAPK and ERK1/2-Dependent NF-κB and AP-1 Activation
    Gao Cheng
    Liu Wei
    Wang Xiurong
    Liu Xiangzhen
    Zhao Shiguang
    Fu Songbin
    CELLULAR AND MOLECULAR NEUROBIOLOGY, 2009, 29 (08) : 1161 - 1168
  • [34] Aciculatin inhibits lipopolysaccharide-mediated inducible nitric oxide synthase and cyclooxygenase-2 expression via suppressing NF-κB and JNK/p38 MAPK activation pathways
    Hsieh, I-Ni
    Chang, Anita Shin-Yuan
    Teng, Che-Ming
    Chen, Chien-Chih
    Yang, Chia-Ron
    JOURNAL OF BIOMEDICAL SCIENCE, 2011, 18
  • [35] Aciculatin inhibits lipopolysaccharide-mediated inducible nitric oxide synthase and cyclooxygenase-2 expression via suppressing NF-κB and JNK/p38 MAPK activation pathways
    I-Ni Hsieh
    Anita Shin-Yuan Chang
    Che-Ming Teng
    Chien-Chih Chen
    Chia-Ron Yang
    Journal of Biomedical Science, 18
  • [36] Moxifloxacin but not ciprofloxacin or azithromycin selectively inhibits IL-8, IL-6, ERK1/2, JNK, and NF-κB activation in a cystic fibrosis epithelial cell line
    Blau, Hannah
    Klein, Keren
    Shalit, Itamar
    Halperin, Drora
    Fabian, Ina
    AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2007, 292 (01) : L343 - L352
  • [37] Icariin induces cell differentiation and cell cycle arrest in mouse melanoma B16 cells via Erk1/2-p38-JNK-dependent pathway
    Wang, Dan
    Xu, Wenjuan
    Chen, Xiaoyu
    Han, Jichun
    Yu, Lina
    Gao, Caixia
    Hao, Wenjin
    Liu, Xiaona
    Zheng, Qiusheng
    Li, Defang
    ONCOTARGET, 2017, 8 (59) : 99504 - 99513
  • [38] Methyl-1-hydroxy-2-naphthoate, a novel naphthol derivative, inhibits lipopolysaccharide-induced inflammatory response in macrophages via suppression of NF-κB, JNK and p38 MAPK pathways
    Zhang, Jun-Yan
    Jin, Hong
    Wang, Guang-Fa
    Yu, Peng-Jiu
    Wu, Shao-Yu
    Zhu, Zheng-Guang
    Li, Zhong-Huang
    Tian, Yuan-Xin
    Xu, Wei
    Zhang, Jia-Jie
    Wu, Shu-Guang
    INFLAMMATION RESEARCH, 2011, 60 (09) : 851 - 859
  • [39] Adiponectin-stimulated CXCL8 release in primary human hepatocytes is regulated by ERK1/ERK2, p38 MAPK, NF-κB, and STAT3 signaling pathways
    Wanninger, Josef
    Neumeier, Markus
    Weigert, Johanna
    Bauer, Sabrina
    Weiss, Thomas S.
    Schaeffler, Andreas
    Krempl, Corinna
    Bleyl, Cornelia
    Aslanidis, Charalampos
    Schoelmerich, Juergen
    Buechler, Christa
    AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2009, 297 (03): : G611 - G618
  • [40] Newly Synthesized 'Hidabeni' Chalcone Derivatives Potently Suppress LPS-Induced NO Production via Inhibition of STAT1, but Not NF-κB, JNK, and p38, Pathways in Microglia
    Hara, Hirokazu
    Ikeda, Ryoko
    Ninomiya, Masayuki
    Kamiya, Tetsuro
    Koketsu, Mamoru
    Adachi, Tetsuo
    BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2014, 37 (06) : 1042 - 1049