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Glycolysis, monocarboxylate transport, and purinergic signaling are key events in Eimeria bovis-induced NETosis

The protozoan parasite Eimeria bovis is the causative agent of bovine coccidiosis, an enteric disease of global importance that significantly affects cattle productivity. Previous studies showed that bovine NETosis—an important early host innate effector mechanism of polymorphonuclear neutrophil (PM...

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Autores principales: Conejeros, Iván, López-Osorio, Sara, Zhou, Ershun, Velásquez, Zahady D., Del Río, María Cristina, Burgos, Rafael Agustín, Alarcón, Pablo, Chaparro-Gutiérrez, Jenny Jovana, Hermosilla, Carlos, Taubert, Anja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403323/
https://www.ncbi.nlm.nih.gov/pubmed/36032127
http://dx.doi.org/10.3389/fimmu.2022.842482
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author Conejeros, Iván
López-Osorio, Sara
Zhou, Ershun
Velásquez, Zahady D.
Del Río, María Cristina
Burgos, Rafael Agustín
Alarcón, Pablo
Chaparro-Gutiérrez, Jenny Jovana
Hermosilla, Carlos
Taubert, Anja
author_facet Conejeros, Iván
López-Osorio, Sara
Zhou, Ershun
Velásquez, Zahady D.
Del Río, María Cristina
Burgos, Rafael Agustín
Alarcón, Pablo
Chaparro-Gutiérrez, Jenny Jovana
Hermosilla, Carlos
Taubert, Anja
author_sort Conejeros, Iván
collection PubMed
description The protozoan parasite Eimeria bovis is the causative agent of bovine coccidiosis, an enteric disease of global importance that significantly affects cattle productivity. Previous studies showed that bovine NETosis—an important early host innate effector mechanism of polymorphonuclear neutrophil (PMN)—is elicited by E. bovis stages. So far, the metabolic requirements of E. bovis-triggered NET formation are unknown. We here studied early glycolytic and mitochondrial responses of PMN as well as the role of pH, distinct metabolic pathways, P2 receptor-mediated purinergic signaling, and monocarboxylate transporters 1 and 2 (MCT1, MCT2) in E. bovis sporozoite-induced NET formation. Seahorse-based experiments revealed a rapid induction of both neutrophil oxygen consumption rate (OCR) and early glycolytic responses, thereby reflecting immediate PMN activation and metabolic changes upon confrontation with sporozoites. The impact of these metabolic changes on NET formation was studied via chemical inhibition experiments targeting glycolysis and energy generation by the use of 2-fluor-2-deoxy-D-glucose (FDG), 6-diazo-5-oxo-L-norleucin (DON), sodium dichloroacetate (DCA), oxythiamine (OT), sodium oxamate (OXA), and oligomycin A (OmA) to block glycolysis, glutaminolysis, pyruvate dehydrogenase kinase, pyruvate dehydrogenase, lactate dehydrogenase, and mitochondrial ATP-synthase, respectively. Overall, sporozoite-induced NET formation was significantly diminished via PMN pretreatments with OmA and OXA, thereby indicating a key role of ATP- and lactate-mediated metabolic pathways. Consequently, we additionally studied the effects of extracellular pH, MCT1, MCT2, and purinergic receptor inhibitors (AR-C141900, AR-C155858, theobromine, and NF449, respectively). Pretreatment with the latter inhibitors led to blockage of sporozoite-triggered DNA release from exposed bovine PMN. This report provides first evidence on the pivotal role of carbohydrate-related metabolic pathways and purinergic receptors being involved in E. bovis sporozoite-induced NETosis.
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spelling pubmed-94033232022-08-26 Glycolysis, monocarboxylate transport, and purinergic signaling are key events in Eimeria bovis-induced NETosis Conejeros, Iván López-Osorio, Sara Zhou, Ershun Velásquez, Zahady D. Del Río, María Cristina Burgos, Rafael Agustín Alarcón, Pablo Chaparro-Gutiérrez, Jenny Jovana Hermosilla, Carlos Taubert, Anja Front Immunol Immunology The protozoan parasite Eimeria bovis is the causative agent of bovine coccidiosis, an enteric disease of global importance that significantly affects cattle productivity. Previous studies showed that bovine NETosis—an important early host innate effector mechanism of polymorphonuclear neutrophil (PMN)—is elicited by E. bovis stages. So far, the metabolic requirements of E. bovis-triggered NET formation are unknown. We here studied early glycolytic and mitochondrial responses of PMN as well as the role of pH, distinct metabolic pathways, P2 receptor-mediated purinergic signaling, and monocarboxylate transporters 1 and 2 (MCT1, MCT2) in E. bovis sporozoite-induced NET formation. Seahorse-based experiments revealed a rapid induction of both neutrophil oxygen consumption rate (OCR) and early glycolytic responses, thereby reflecting immediate PMN activation and metabolic changes upon confrontation with sporozoites. The impact of these metabolic changes on NET formation was studied via chemical inhibition experiments targeting glycolysis and energy generation by the use of 2-fluor-2-deoxy-D-glucose (FDG), 6-diazo-5-oxo-L-norleucin (DON), sodium dichloroacetate (DCA), oxythiamine (OT), sodium oxamate (OXA), and oligomycin A (OmA) to block glycolysis, glutaminolysis, pyruvate dehydrogenase kinase, pyruvate dehydrogenase, lactate dehydrogenase, and mitochondrial ATP-synthase, respectively. Overall, sporozoite-induced NET formation was significantly diminished via PMN pretreatments with OmA and OXA, thereby indicating a key role of ATP- and lactate-mediated metabolic pathways. Consequently, we additionally studied the effects of extracellular pH, MCT1, MCT2, and purinergic receptor inhibitors (AR-C141900, AR-C155858, theobromine, and NF449, respectively). Pretreatment with the latter inhibitors led to blockage of sporozoite-triggered DNA release from exposed bovine PMN. This report provides first evidence on the pivotal role of carbohydrate-related metabolic pathways and purinergic receptors being involved in E. bovis sporozoite-induced NETosis. Frontiers Media S.A. 2022-08-11 /pmc/articles/PMC9403323/ /pubmed/36032127 http://dx.doi.org/10.3389/fimmu.2022.842482 Text en Copyright © 2022 Conejeros, López-Osorio, Zhou, Velásquez, Del Río, Burgos, Alarcón, Chaparro-Gutiérrez, Hermosilla and Taubert https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Conejeros, Iván
López-Osorio, Sara
Zhou, Ershun
Velásquez, Zahady D.
Del Río, María Cristina
Burgos, Rafael Agustín
Alarcón, Pablo
Chaparro-Gutiérrez, Jenny Jovana
Hermosilla, Carlos
Taubert, Anja
Glycolysis, monocarboxylate transport, and purinergic signaling are key events in Eimeria bovis-induced NETosis
title Glycolysis, monocarboxylate transport, and purinergic signaling are key events in Eimeria bovis-induced NETosis
title_full Glycolysis, monocarboxylate transport, and purinergic signaling are key events in Eimeria bovis-induced NETosis
title_fullStr Glycolysis, monocarboxylate transport, and purinergic signaling are key events in Eimeria bovis-induced NETosis
title_full_unstemmed Glycolysis, monocarboxylate transport, and purinergic signaling are key events in Eimeria bovis-induced NETosis
title_short Glycolysis, monocarboxylate transport, and purinergic signaling are key events in Eimeria bovis-induced NETosis
title_sort glycolysis, monocarboxylate transport, and purinergic signaling are key events in eimeria bovis-induced netosis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403323/
https://www.ncbi.nlm.nih.gov/pubmed/36032127
http://dx.doi.org/10.3389/fimmu.2022.842482
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