RETRACTED: Activation of murine peritoneal macrophages by sulfated exopolysaccharide from marine microalgal Gyrodinium impudicum (strain KG03):: Involvement of the NF-κB and JNK pathway (Retracted article. See vol. 99, 2021)

被引:37
作者
Bae, SY
Yim, JH
Lee, HK
Pyo, S [1 ]
机构
[1] Sungkyunkwan Univ, Coll Pharm, Div Immunopharmacol, Suwon 440746, Kyunggi, South Korea
[2] KORDI, Korea Polar Res Inst, Ansan 425600, Kyunggi, South Korea
关键词
Gyrodinium impudicum; microalgal sulfated exopolysaccharide; macrophages; tumoricidal activity; NF-kappa B; JNK;
D O I
10.1016/j.intimp.2005.09.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
This study examined the ability of microalgal sulfated exopolysaccharide (MSE) from marine microalgal Gyrodinium impudicum (strain KG03) to induce secretory and cellular responses in murine peritoneal macrophages. The cytotoxicity induced by preincubating tumor cells with MSE was demonstrated to be concentration-dependent. The MSE-induced tumoricidal activity was partially abrogated by a NO inhibitor, whereas the anti-TNF-alpha and anti-IFN-alpha/beta antibodies as well as the scavengers of reactive oxygen intermediates had no effect. In addition, supernatants from murine peritoneal macrophages treated with MSE contained nitrite and their iNOS enzymatic activity was significantly increased. Therefore, the tumoricidal activity induced by MSE appeared to be mediated by the production of NO. Treating the macrophages with a JNK inhibitor (SP600125) partially blocked the tumoricidal activation and NO production induced by MSE, whereas inhibitors of the other kinases did not have an inhibitory effect. These results suggest that MSE induces NO production via the JNK dependent pathway. Furthermore, electrophoretic mobility shift assay analyses revealed that the MSE treatment induced the activation of the NF-kappa B transcription factor. Overall, these results indicate that the tumoricidal activity induced by MSE is mainly due to NO production, and the activation of macrophage by MSE is mediated probably via the NF-kappa B and JNK pathway. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:473 / 484
页数:12
相关论文
共 55 条
[1]
Evidence for nucleotide receptor modulation of cross talk between MAP kinase and NF-κB signaling pathways in murine RAW 264.7 macrophages [J].
Aga, M ;
Watters, JJ ;
Pfeiffer, ZA ;
Wiepz, GJ ;
Sommer, JA ;
Bertics, PJ .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 286 (04) :C923-C930
[2]
Safflower polysaccharides activate the transcription factor NF-κB via Toll-like receptor 4 and induce cytokine production by macrophages [J].
Ando, I ;
Tsukumo, Y ;
Wakabayashi, T ;
Akashi, S ;
Miyake, K ;
Kataoka, T ;
Nagai, K .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2002, 2 (08) :1155-1162
[3]
ARDEN L, 1985, LYMPHOKINES, V10, P175
[4]
INTERFERONS AS MACROPHAGE-ACTIVATING FACTORS .2. ENHANCED SECRETION OF INTERLEUKIN-1 BY LIPOPOLYSACCHARIDE-STIMULATED HUMAN-MONOCYTES [J].
ARENZANASEISDEDOS, F ;
VIRELIZIER, JL .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1983, 13 (06) :437-440
[5]
BATINIC D, 1992, J BIOL CHEM, V267, P6664
[6]
Boisson-Vidal C., 1995, Drugs of the Future, V20, P1237
[7]
COMPOSITION AND ANTIVIRAL ACTIVITIES OF A SULFATED POLYSACCHARIDE FROM SCHIZYMENIA-DUBYI (RHODOPHYTA, GIGARTINALES) [J].
BOURGOUGNON, N ;
LAHAYE, M ;
CHERMANN, JC ;
KORNPROBST, JM .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1993, 3 (06) :1141-1146
[8]
NF-κB family of transcription factors:: Central regulators of innate and adaptive immune functions [J].
Caamaño, J ;
Hunter, CA .
CLINICAL MICROBIOLOGY REVIEWS, 2002, 15 (03) :414-+
[9]
Potential role of the JNK/SAPK signal transduction pathway in the induction of iNOS by TNF-α [J].
Chan, ED ;
Riches, DWH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 253 (03) :790-796
[10]
Induction of apoptosis and expression of apoptosis related genes in human epithelial carcinoma cells by Helicobacter pylori VacA toxin [J].
Cho, SJ ;
Kang, NS ;
Park, SY ;
Kim, BO ;
Rhee, DK ;
Pyo, S .
TOXICON, 2003, 42 (06) :601-611