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Mitochondria-induced formation of neutrophil extracellular traps is enhanced in the elderly via Toll-like receptor 9

Neutrophil extracellular traps are potent antimicrobial weapons; however, their formation during sterile inflammation is detrimental, and the mechanism of induction is still unclear. Since advanced age is the primary clinical risk factor for poor outcomes in inflammatory diseases, we hypothesized th...

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Published in:Journal of leukocyte biology 2023-11, Vol.114 (6), p.651-665
Main Authors: Pastorek, Michal, Konečná, Barbora, Janko, Jakub, Janovičová, Ľubica, Podracká, Ľudmila, Záhumenský, Jozef, Šteňová, Emöke, Dúbrava, Martin, Hodosy, Július, Vlková, Barbora, Celec, Peter
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container_title Journal of leukocyte biology
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creator Pastorek, Michal
Konečná, Barbora
Janko, Jakub
Janovičová, Ľubica
Podracká, Ľudmila
Záhumenský, Jozef
Šteňová, Emöke
Dúbrava, Martin
Hodosy, Július
Vlková, Barbora
Celec, Peter
description Neutrophil extracellular traps are potent antimicrobial weapons; however, their formation during sterile inflammation is detrimental, and the mechanism of induction is still unclear. Since advanced age is the primary clinical risk factor for poor outcomes in inflammatory diseases, we hypothesized that sterile stimuli, represented by mitochondria, would induce neutrophil extracellular trap formation in an age-dependent manner. Therefore, we analyzed induction of neutrophil extracellular traps in patients grouped according to age or immune status and observed that neutrophils from elderly patients responded to the presence of mitochondria with enhanced neutrophil extracellular trap formation. These neutrophil extracellular traps were also found to be more oxidized and exhibited higher resistance to DNase I degradation. Additionally, a higher concentration of residual neutrophil extracellular traps was detected in the plasma of the elderly. This plasma was capable of priming neutrophils through TLR9-mediated signaling, leading to further neutrophil extracellular trap formation, which was successfully inhibited with chloroquine. Finally, in a mouse model of mitochondria-induced acute lung injury, we observed that neutrophils from aged mice displayed impaired chemotactic activity but exhibited a trend of higher neutrophil extracellular trap formation. Thus, we propose that residual neutrophil extracellular traps circulating in the elderly preactivate neutrophils, making them more prone to enhanced neutrophil extracellular trap formation when exposed to mitochondria during sterile inflammation. Further investigation is needed to determine whether this vicious circle could be a suitable therapeutic target.
doi_str_mv 10.1093/jleuko/qiad101
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Finally, in a mouse model of mitochondria-induced acute lung injury, we observed that neutrophils from aged mice displayed impaired chemotactic activity but exhibited a trend of higher neutrophil extracellular trap formation. Thus, we propose that residual neutrophil extracellular traps circulating in the elderly preactivate neutrophils, making them more prone to enhanced neutrophil extracellular trap formation when exposed to mitochondria during sterile inflammation. 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subjects Aged
Animals
Extracellular Traps
Humans
Inflammation - metabolism
Mice
Mitochondria - metabolism
Neutrophils
Toll-Like Receptor 9 - metabolism
title Mitochondria-induced formation of neutrophil extracellular traps is enhanced in the elderly via Toll-like receptor 9
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