Highly purified glycosylphosphatidylinositols from Trypanosoma cruzi are potent proinflammatory agents

被引:202
作者
Almeida, IC
Camargo, MM
Procópio, DO
Silva, LS
Mehlert, A
Travassos, LR
Gazzinelli, RT
Ferguson, MAJ [1 ]
机构
[1] Univ Dundee, Dept Biochem, Div Mol Parasitol & Biol Chem, Dundee DD1 5EH, Scotland
[2] Univ Fed Minas Gerais, Dept Biochem & Immunol, Belo Horizonte, MG, Brazil
[3] Univ Fed Sao Paulo, Dept Microbiol Immunol & Parasitol, Discipline Cell Biol, BR-0423062 Sao Paulo, Brazil
[4] Fundacao Oswaldo Cruz, Ctr Pesquisas Rene Rachou, BR-30190002 Belo Horizonte, MG, Brazil
关键词
Chagas' disease; cytokines; glycosylphosphatidylinositol; inflammation; nitric oxide;
D O I
10.1093/emboj/19.7.1476
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Intracellular protozoan parasites are potent stimulators of cell-mediated immunity. The induction of macrophage proinflammatory cytokines by Trypanosoma cruzi is considered to be important in controlling the infection and the outcome of Chagas' disease. Here we show that the potent tumour necrosis factor-alpha-, interleukin-12- and nitric oxide-inducing activities of T.cruzi trypomastigote mucins were recovered quantitatively in a highly purified and characterized glycosylphosphatidylinositol (GPI) anchor fraction of this material. The bioactive trypomastigote GPI fraction was compared with a relatively inactive GPI fraction prepared from T.cruzi epimastigote mucins, The trypomastigote GPI structures were found to contain additional galactose residues and unsaturated, instead of saturated, fatty acids in the sn-2 position of the alkyl-acylglycerolipid component. The latter feature is essential for the extreme potency of the trypomastigote GPI fraction, which is at least as active as bacterial endotoxin and Mycoplasma lipopeptide and, therefore, one of the most potent microbial proinflammatory agents known.
引用
收藏
页码:1476 / 1485
页数:10
相关论文
共 50 条
[21]   Two distinct groups of mucin-like genes are differentially expressed in the developmental stages of Trypanosoma cruzi [J].
Freitas-Junior, LHG ;
Briones, MRS ;
Schenkman, S .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1998, 93 (01) :101-114
[22]   INTERLEUKIN-12 IS REQUIRED FOR THE T-LYMPHOCYTE-INDEPENDENT INDUCTION OF INTERFERON-GAMMA BY AN INTRACELLULAR PARASITE AND INDUCES RESISTANCE IN T-CELL-DEFICIENT HOSTS [J].
GAZZINELLI, RT ;
HIENY, S ;
WYNN, TA ;
WOLF, S ;
SHER, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (13) :6115-6119
[23]   GALACTOFURANOSE-CONTAINING GLYCOCONJUGATES OF EPIMASTIGOTE AND TRYPOMASTIGOTE FORMS OF TRYPANOSOMA-CRUZI [J].
GOLGHER, DB ;
COLLI, W ;
SOUTOPADRON, T ;
ZINGALES, B .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1993, 60 (02) :249-264
[24]  
GUTHER MLS, 1992, J BIOL CHEM, V267, P6820
[25]   IMMUNOHISTOCHEMICAL CHARACTERIZATION OF INFILTRATING CELLS IN HUMAN CHRONIC CHAGASIC MYOCARDITIS - COMPARISON WITH MYOCARDIAL REJECTION PROCESS [J].
HIGUCHI, MD ;
GUTIERREZ, PS ;
AIELLO, VD ;
PALOMINO, S ;
BOCCHI, E ;
KALIL, J ;
BELLOTTI, G ;
PILEGGI, F .
VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY, 1993, 423 (03) :157-160
[26]   DEVELOPMENT OF TH1 CD4+ T-CELLS THROUGH IL-12 PRODUCED BY LISTERIA-INDUCED MACROPHAGES [J].
HSIEH, CS ;
MACATONIA, SE ;
TRIPP, CS ;
WOLF, SF ;
OGARRA, A ;
MURPHY, KM .
SCIENCE, 1993, 260 (5107) :547-549
[27]   Transfer of exogenous glycosylphos-phatidylinositol (GPI)-linked molecules to plasma membranes [J].
Ilangumaran, S ;
Robinson, PJ ;
Hoessli, DC .
TRENDS IN CELL BIOLOGY, 1996, 6 (05) :163-167
[28]   AMPLIFICATION OF A TRYPANOSOMA-CRUZI DNA-SEQUENCE FROM INFLAMMATORY LESIONS IN HUMAN CHAGASIC CARDIOMYOPATHY [J].
JONES, EM ;
COLLEY, DG ;
TOSTES, S ;
LOPES, ER ;
VNENCAKJONES, CL ;
MCCURLEY, TL .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1993, 48 (03) :348-357
[29]  
Magez S, 1998, J IMMUNOL, V160, P1949
[30]   Cell-surface engineering with GPI-anchored proteins [J].
Medof, ME ;
Nagarajan, S ;
Tykocinski, ML .
FASEB JOURNAL, 1996, 10 (05) :574-586