Abstract

NETosis is a neutrophil process involving sequential steps from pathogen detection to the release of DNA harboring antimicrobial proteins, including the central generation of NADPH oxidase dependent or independent ROS. Previously, we reported that NETosis triggered by Entamoeba histolytica trophozoites is independent of NADPH oxidase activity in neutrophils, but dependent on the viability of the parasites and no ROS source was identified. Here, we explored the possibility that E. histolytica trophozoites serve as the ROS source for NETosis. NET quantitation was performed using SYTOX® Green assay in the presence of selective inhibitors and scavengers. We observed that respiratory burst in neutrophils was inhibited by trophozoites in a dose dependent manner. Mitochondrial ROS was not also necessary, as the mitochondrial scavenger mitoTEMPO did not affect the process. Surprisingly, ROS-deficient amoebas obtained by pre-treatment with pyrocatechol were less likely to induce NETs. Additionally, we detected the presence of MPO on the cell surface of trophozoites after the interaction with neutrophils and found that luminol and isoluminol, intracellular and extracellular scavengers for MPO derived ROS reduced the amount of NET triggered by amoebas. These data suggest that ROS generated by trophozoites and processed by the extracellular MPO during the contact with neutrophils are required for E. histolytica induced NETosis.

Highlights

  • Neutrophil extracellular traps (NETs) are DNA fibers associated with histones and antimicrobial proteins that are released by neutrophils into the extracellular space in a process denominated NETosis [1]

  • We previously showed that E. histolytica trophozoites induce a rapid NETosis in human neutrophils that is dependent on the viability of the parasite but independent of NADPH oxidase and PAD4 activities [41]

  • The case of NETosis induced by the E. histolytica trophozoites is intriguing, as we showed that the process occurs through a non-classical mechanism, independent of NADPH-reactive oxygen species (ROS) and PAD4 activity [41,45]

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Summary

Introduction

Neutrophil extracellular traps (NETs) are DNA fibers associated with histones and antimicrobial proteins that are released by neutrophils into the extracellular space in a process denominated NETosis [1]. NETs were described as a strategy used for neutrophils to entrap and kill microorganisms [2,3,4,5]; these structures have been related to other processes such as coagulation or complement activation, and even with autoimmune pathological processes such as erythematous systemic lupus [6,7,8]. Neutrophils detect pathogens through receptors on cell surface such as TLRs, dectins, integrins or antibody receptors [12,13,14,15].

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