[HTML][HTML] Trypanosoma cruzi and Its Soluble Antigens Induce NET Release by Stimulating Toll-Like Receptors

D Sousa-Rocha, M Thomaz-Tobias, LFA Diniz… - PloS one, 2015 - journals.plos.org
D Sousa-Rocha, M Thomaz-Tobias, LFA Diniz, PSS Souza, P Pinge-Filho, KA Toledo
PloS one, 2015journals.plos.org
Neutrophils release fibrous traps of DNA, histones, and granule proteins known as
neutrophil extracellular traps (NETs), which contribute to microbicidal killing and have been
implicated in autoimmunity. The role of NET formation in the host response to nonbacterial
pathogens is not well-understood. In this study, we investigated the release of NETs by
human neutrophils upon their interaction with Trypanosoma cruzi (Y strain) parasites. Our
results showed that human neutrophils stimulated by T. cruzi generate NETs composed of …
Neutrophils release fibrous traps of DNA, histones, and granule proteins known as neutrophil extracellular traps (NETs), which contribute to microbicidal killing and have been implicated in autoimmunity. The role of NET formation in the host response to nonbacterial pathogens is not well-understood. In this study, we investigated the release of NETs by human neutrophils upon their interaction with Trypanosoma cruzi (Y strain) parasites. Our results showed that human neutrophils stimulated by T. cruzi generate NETs composed of DNA, histones, and elastase. The release occurred in a dose-, time-, and reactive oxygen species-dependent manner to decrease trypomastigote and increase amastigote numbers of the parasites without affecting their viability. NET release was decreased upon blocking with antibodies against Toll-like receptors 2 and 4. In addition, living parasites were not mandatory in the release of NETs induced by T. cruzi, as the same results were obtained when molecules from its soluble extract were tested. Our results increase the understanding of the stimulation of NETs by parasites, particularly T. cruzi. We suggest that contact of T. cruzi with NETs during Chagas’s disease can limit infection by affecting the infectivity/pathogenicity of the parasite.
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