Down regulation of NO signaling in Trypanosoma cruzi upon parasite-extracellular matrix interaction: changes in protein modification by nitrosylation and nitration

Adhesion of the Trypanosoma cruzi trypomastigotes, the causative agent of Chagas' disease in humans, to components of the extracellular matrix (ECM) is an important step in host cell invasion. The signaling events triggered in the parasite upon binding to ECM are less explored and, to our knowl...

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Veröffentlicht in:PLoS neglected tropical diseases 2015-04, Vol.9 (4), p.e0003683-e0003683
Hauptverfasser: Pereira, Milton, Soares, Chrislaine, Canuto, Gisele André Baptista, Tavares, Marina Franco Maggi, Colli, Walter, Alves, Maria Julia M
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container_title PLoS neglected tropical diseases
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Soares, Chrislaine
Canuto, Gisele André Baptista
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Colli, Walter
Alves, Maria Julia M
description Adhesion of the Trypanosoma cruzi trypomastigotes, the causative agent of Chagas' disease in humans, to components of the extracellular matrix (ECM) is an important step in host cell invasion. The signaling events triggered in the parasite upon binding to ECM are less explored and, to our knowledge, there is no data available regarding •NO signaling. Trypomastigotes were incubated with ECM for different periods of time. Nitrated and S-nitrosylated proteins were analyzed by Western blotting using anti-nitrotyrosine and S-nitrosyl cysteine antibodies. At 2 h incubation time, a decrease in NO synthase activity, •NO, citrulline, arginine and cGMP concentrations, as well as the protein modifications levels have been observed in the parasite. The modified proteins were enriched by immunoprecipitation with anti-nitrotyrosine antibodies (nitrated proteins) or by the biotin switch method (S-nitrosylated proteins) and identified by MS/MS. The presence of both modifications was confirmed in proteins of interest by immunoblotting or immunoprecipitation. For the first time it was shown that T. cruzi proteins are amenable to modifications by S-nitrosylation and nitration. When T. cruzi trypomastigotes are incubated with the extracellular matrix there is a general down regulation of these reactions, including a decrease in both NOS activity and cGMP concentration. Notwithstanding, some specific proteins, such as enolase or histones had, at least, their nitration levels increased. This suggests that post-translational modifications of T. cruzi proteins are not only a reflex of NOS activity, implying other mechanisms that circumvent a relatively low synthesis of •NO. In conclusion, the extracellular matrix, a cell surrounding layer of macromolecules that have to be trespassed by the parasite in order to be internalized into host cells, contributes to the modification of •NO signaling in the parasite, probably an essential move for the ensuing invasion step.
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This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: upon Parasite-Extracellular Matrix Interaction: Changes in Protein Modification by Nitrosylation and Nitration. 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subjects Animals
Blotting, Western
Cellular signal transduction
Chagas Disease - metabolism
Down-Regulation
Extracellular matrix
Extracellular Matrix - physiology
Free radicals
Genetic aspects
Humans
Immunoprecipitation
Kinases
Mammals
Motility
Nitric oxide
Nitric Oxide - metabolism
Parasites
Properties
Protein Processing, Post-Translational
Proteins
Protozoa
Signal Transduction - physiology
Tandem Mass Spectrometry
Trypanosoma cruzi
Trypanosoma cruzi - physiology
Tyrosine - analogs & derivatives
Virulence (Microbiology)
title Down regulation of NO signaling in Trypanosoma cruzi upon parasite-extracellular matrix interaction: changes in protein modification by nitrosylation and nitration
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