Use este identificador para citar ou linkar para este item: http://repositorio.ufla.br/jspui/handle/1/32848
Título: Neutrophil-generated HOCL leads to non-specific thiol oxidation in phagocytized bacteria
Data do documento: 2018
Citação: DEGROSSOLI, A. et al. Neutrophil-generated HOCL leads to non-specific thiol oxidation in phagocytized bacteria. Elife, [S.l.], 2018.
Resumo: Phagocytic immune cells kill pathogens in the phagolysosomal compartment with a cocktail of antimicrobial agents. Chief among them are reactive species produced in the so-called oxidative burst. Here, we show that bacteria exposed to a neutrophil-like cell line experience a rapid and massive oxidation of cytosolic thiols. Using roGFP2-based fusion probes, we could show that this massive breakdown of the thiol redox homeostasis was dependent on phagocytosis, presence of NADPH oxidase and ultimately myeloperoxidase. Interestingly, the redox-mediated fluorescence change in bacteria expressing a glutathione-specific Grx1-roGFP2 fusion protein or an unfused roGFP2 showed highly similar reaction kinetics to the ones observed with roGFP2-Orp1, under all conditions tested. We recently observed such an indiscriminate oxidation of roGFP2-based fusion probes by HOCl with fast kinetics in vitro. In line with these observations, abating HOCl production in immune cells with a myeloperoxidase inhibitor significantly attenuated the oxidation of all three probes in bacteria.
URI: https://elifesciences.org/articles/32288
http://repositorio.ufla.br/jspui/handle/1/32848
Aparece nas coleções:DME - Artigos publicados em periódicos

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