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FASEB J ; 13(12): 1627-36, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10463955

ABSTRACT

The effects of the glycoinositolphospholipids (GIPLs) fromTrypanosoma cruzi on T lymphocyte activation were investigated in a mouse T cell hybridoma (DO-11.10). Purified GIPLs from T. cruzi strains Y and G markedly increased IL-2 mRNA transcripts and IL-2 secretion induced by mitogenic anti-CD3 and anti-Thy1 mAbs. This costimulatory function was also revealed by the induction of IL-2 secretion after the simultaneous addition of the T. cruzi GIPLs and either the calcium ionophore A23187 or phorbol ester. The capacity of the GIPL molecule to induce an increase in cytoplasmic calcium levels was also demonstrated. After exposure of T cell hybridoma to GIPL, the nuclear transcription factor NFAT1 became partially dephosphorylated, and its nuclear localization was demonstrated both in the T cell hybridoma and in Balb/c CD3(+) cells. These results demonstrate that T. cruzi GIPL molecules are capable of signaling to T cells and therefore could be valuable tools for the study of T cell activation, besides playing a potential role in subverting the T lymphocyte immune response during T. cruzi infection.


Subject(s)
DNA-Binding Proteins/metabolism , Glycolipids/immunology , Interleukin-2/genetics , Lymphocyte Activation , Nuclear Proteins , Phospholipids/immunology , T-Lymphocytes/physiology , Transcription Factors/metabolism , Transcription, Genetic/immunology , Trypanosoma cruzi/immunology , Animals , Antibodies, Monoclonal/pharmacology , CD3 Complex/immunology , Calcimycin/pharmacology , Cell Line , Cell Nucleus/drug effects , Cell Nucleus/physiology , Gene Expression Regulation/drug effects , Gene Expression Regulation/immunology , Glycolipids/isolation & purification , Glycolipids/pharmacology , Hybridomas/drug effects , Hybridomas/immunology , Hybridomas/physiology , Interleukin-2/metabolism , Mice , Mice, Inbred BALB C , NFATC Transcription Factors , Phospholipids/isolation & purification , Phospholipids/pharmacology , Phosphorylation , T-Lymphocytes/drug effects , T-Lymphocytes/immunology , Th1 Cells/immunology , Transcription, Genetic/drug effects
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