Macrophage signaling by glycosylphosphatidylinositol-anchored mucin-like glycoproteins derived from Trypanosoma cruzi trypomastigotes

被引:57
|
作者
Ropert, C
Ferreira, LRP
Campos, MAS
Procópio, DO
Travassos, LR
Ferguson, MAJ
Reis, LFL
Teixeira, MM
Almeida, IC
Gazzinelli, RT
机构
[1] Fiocruz MS, CPqRR, Immunopathol Lab, BR-30190002 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, ICB, Dept Biochem & Immunol, BR-31270901 Belo Horizonte, MG, Brazil
[3] Ludwig Inst Canc Res, BR-01509010 Sao Paulo, Brazil
[4] Univ Fed Sao Paulo, Expt Oncol Unit, BR-04023062 Sao Paulo, Brazil
[5] Univ Dundee, Dept Biochem, Dundee DD1 5EH, Scotland
[6] Univ Sao Paulo, ICB, Dept Parasitol, BR-05508900 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Trypanosoma cruzi; GPI anchors; TLR-2; macrophages; chemokines;
D O I
10.1016/S1286-4579(02)01609-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Activation of cells from the innate immune system has an important role in host resistance to early infection with the intracellular protozoan parasite, Trypanosoma cruzi. Here we review the studies that have identified and structurally characterized the glycosylphosphatidylinositol (GPI) anchors, as parasite molecules responsible for the activation of cells from the macrophage lineage. We also cover the studies that have identified the receptor, signaling pathways as well as the array of genes expressed in macrophages that are activated by these glycoconjugates. We discuss the possible-implications of such response on the host resistance to T. cruzi infection and the pathogenesis of Chagas disease. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:1015 / 1025
页数:11
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