Artículos de revistas
Trans-sialidase from Trypanosoma cruzi enhances the adhesion properties and fibronectin-driven migration of thymocytes
Fecha
2013-02Registro en:
Nardy, Ana Flávia F.R.; Silva Filho, Joao Luiz da; Perez, Ana Rosa; Meis, Juliana de; Farias de Oliveira, Désio Aurélio; et al.; Trans-sialidase from Trypanosoma cruzi enhances the adhesion properties and fibronectin-driven migration of thymocytes; Elsevier Science; Microbes and Infection; 15; 5; 2-2013; 365-374
1286-4579
CONICET Digital
CONICET
Autor
Nardy, Ana Flávia F.R.
Silva Filho, Joao Luiz da
Perez, Ana Rosa
Meis, Juliana de
Farias de Oliveira, Désio Aurélio
Penha, Luciana
Oliveira, Isadora de Araújo
Dias, Wagner B.
Todeschini, Adriane
Freire de Lima, Célio Geraldo
Bellio, Maria
Caruso Neves, Celso
Pinheiro, Ana Acácia
Takiya, Christina Maeda
Bottasso, Oscar Adelmo
Savino, Wilson
Morrot, Alexandre
Resumen
In experimental Trypanosoma cruzi infections, severe thymic atrophy leads to release of activated CD4+CD8+ double-positive (DP) T cells to the periphery. In humans, activated DP T cells are found in the blood in association with severe cardiac forms of human chronic Chagas disease. The mechanisms underlying the premature thymocyte release during the chagasic thymic atrophy remain elusive. We tested whether the migratory properties of intrathymic thymocytes are modulated by the parasite trans-sialidase (TS). We found that TS affected the dynamics of thymocytes undergoing intrathymic maturation, and these changes were accompanied by an increase in the number of recent DP thymic emigrants in the peripheral lymphoid organs. We demonstrated that increased percentages of blood DP T cell subsets were associated with augmented antibody titers against TS in chagasic patients with chronic cardiomyopathy. In vitro studies showed that TS was able to activate the MAPK pathway and actin filament mobilization in thymocytes. These effects were correlated with its ability to modulate the adhesion of thymocytes to thymic epithelial cells and their migration toward extracellular matrix. These findings point to effects of TS that could influence the escape of immature thymocytes in Chagas disease.