The anacardic 6-pentadecyl salicylic acid induces macrophage activation via the phosphorylation of ERK1/2, JNK, P38 kinases and NF-κB

被引:29
|
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
  • [1] Cry1Ac toxin induces macrophage activation via ERK1/2, JNK and p38 mitogen-activated protein kinases
    Torres-Martinez, Marilu
    Rubio-Infante, Nestor
    Lilia Garcia-Hernandez, Ana
    Nava-Acosta, Raul
    Ilhuicatzi-Alvarado, Damaris
    Moreno-Fierros, Leticia
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2016, 78 : 106 - 115
  • [2] Protocatechuic Acid from Alpinia oxyphylla Induces Schwann Cell Migration via ERK1/2, JNK and p38 Activation
    Ju, Da-Tong
    Kuo, Wei-Wen
    Ho, Tsung-Jung
    Paul, Catherine Reena
    Kuo, Chia-Hua
    Viswanadha, Vijaya Padma
    Lin, Chien-Chung
    Chen, Yueh-Sheng
    Chang, Yung-Ming
    Huang, Chih-Yang
    AMERICAN JOURNAL OF CHINESE MEDICINE, 2015, 43 (04): : 653 - 665
  • [3] Stimulation of Macrophage TNFα Production by Orthopaedic Wear Particles Requires Activation of the ERK1/2/Egr-1 and NF-κB Pathways But Is Independent of p38 and JNK
    Beidelschies, Michelle A.
    Huang, Honglian
    McMullen, Megan R.
    Smith, Matthew V.
    Islam, Andrew S.
    Goldberg, Victor M.
    Chen, Xin
    Nagy, Laura E.
    Greenfield, Edward M.
    JOURNAL OF CELLULAR PHYSIOLOGY, 2008, 217 (03) : 652 - 666
  • [4] Adenosine 5′-monophosphate-induced hypothermia inhibits the activation of ERK1/2, JNK, p38 and NF-κB in endotoxemic rats
    Wang, Yunlong
    Zhang, Aihua
    Lu, Shulai
    Pan, Xinting
    Jia, Dongmei
    Yu, Wenjuan
    Jiang, Yanxia
    Li, Xinde
    Wang, Xuefeng
    Zhang, Jidong
    Hou, Lin
    Sun, Yunbo
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2014, 23 (01) : 205 - 210
  • [5] Src and Cas mediate JNK activation but not ERK1/2 and p38 kinases by reactive oxygen species
    Yoshizumi, M
    Abe, J
    Haendeler, J
    Huang, QH
    Berk, BC
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (16) : 11706 - 11712
  • [6] Infectious bursal disease virus infection induces macrophage activation via p38 MAPK and NF-κB pathways
    Khatri, Mahesh
    Sharma, Jagdev M.
    VIRUS RESEARCH, 2006, 118 (1-2) : 70 - 77
  • [7] Transcriptional Down-Regulation of Thromboxane A2 Receptor Expression via Activation of MAPK ERK1/2, p38/NF-κB Pathways
    Zhang, Wei
    Zhang, Yaping
    Edvinsson, Lars
    Xu, Cang-Bao
    JOURNAL OF VASCULAR RESEARCH, 2009, 46 (02) : 162 - 174
  • [8] Sphinganine induces phosphorylation of ERK1/ERK2, JNK1/JNK2, and p38 mitogen activated protein kinases in HT-29 human colon cancer cells.
    Ahn, EH
    Schroeder, JJ
    FASEB JOURNAL, 2002, 16 (05): : A974 - A974
  • [9] Ubiquitination and translocation of TRAF2 is required for activation of JNK but not of p38 or NF-κB
    Habelhah, H
    Takahashi, S
    Cho, SG
    Kadoya, T
    Watanabe, T
    Ronai, Z
    EMBO JOURNAL, 2004, 23 (02): : 322 - 332
  • [10] Azilsartan Modulates HMGB1/NF-κB/p38/ERK1/2/JNK and Apoptosis Pathways during Renal Ischemia Reperfusion Injury
    Alaaeldin, Rania
    Bakkar, Sally M.
    Mohyeldin, Reham H.
    Ali, Fares E. M.
    Abdel-Maqsoud, Nehad M. Reda
    Fathy, Moustafa
    CELLS, 2023, 12 (01)