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Regulating NETosis: Increasing pH Promotes NADPH Oxidase-Dependent NETosis

Neutrophils migrating from the blood (pH 7.35–7.45) into the surrounding tissues encounter changes in extracellular pH (pH(e)) conditions. Upon activation of NADPH oxidase 2 (Nox), neutrophils generate large amounts of H(+) ions reducing the intracellular pH (pH(i)). Nevertheless, how extracellular...

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Autores principales: Khan, Meraj A., Philip, Lijy M., Cheung, Guillaume, Vadakepeedika, Shawn, Grasemann, Hartmut, Sweezey, Neil, Palaniyar, Nades
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816902/
https://www.ncbi.nlm.nih.gov/pubmed/29487850
http://dx.doi.org/10.3389/fmed.2018.00019
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author Khan, Meraj A.
Philip, Lijy M.
Cheung, Guillaume
Vadakepeedika, Shawn
Grasemann, Hartmut
Sweezey, Neil
Palaniyar, Nades
author_facet Khan, Meraj A.
Philip, Lijy M.
Cheung, Guillaume
Vadakepeedika, Shawn
Grasemann, Hartmut
Sweezey, Neil
Palaniyar, Nades
author_sort Khan, Meraj A.
collection PubMed
description Neutrophils migrating from the blood (pH 7.35–7.45) into the surrounding tissues encounter changes in extracellular pH (pH(e)) conditions. Upon activation of NADPH oxidase 2 (Nox), neutrophils generate large amounts of H(+) ions reducing the intracellular pH (pH(i)). Nevertheless, how extracellular pH regulates neutrophil extracellular trap (NET) formation (NETosis) is not clearly established. We hypothesized that increasing pH increases Nox-mediated production of reactive oxygen species (ROS) and neutrophil protease activity, stimulating NETosis. Here, we found that raising pH(e) (ranging from 6.6 to 7.8; every 0.2 units) increased pH(i) of both activated and resting neutrophils within 10–20 min (Seminaphtharhodafluor dual fluorescence measurements). Since Nox activity generates H(+) ions, pH(i) is lower in neutrophils that are activated compared to resting. We also found that higher pH stimulated Nox-dependent ROS production (R123 generation; flow cytometry, plate reader assay, and imaging) during spontaneous and phorbol myristate acetate-induced NETosis (Sytox Green assays, immunoconfocal microscopy, and quantifying NETs). In neutrophils that are activated and not resting, higher pH stimulated histone H4 cleavage (Western blots) and NETosis. Raising pH increased Escherichia coli lipopolysaccharide-, Pseudomonas aeruginosa (Gram-negative)-, and Staphylococcus aureus (Gram-positive)-induced NETosis. Thus, higher pH(e) promoted Nox-dependent ROS production, protease activity, and NETosis; lower pH has the opposite effect. These studies provided mechanistic steps of pH(e)-mediated regulation of Nox-dependent NETosis. Raising pH either by sodium bicarbonate or Tris base (clinically known as Tris hydroxymethyl aminomethane, tromethamine, or THAM) increases NETosis. Each Tris molecule can bind 3H(+) ions, whereas each bicarbonate HCO3(−) ion binds 1H(+) ion. Therefore, the amount of Tris solution required to cause the same increase in pH level is less than that of equimolar bicarbonate solution. For that reason, regulating NETosis by pH with specific buffers such as THAM could be more effective than bicarbonate in managing NET-related diseases.
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spelling pubmed-58169022018-02-27 Regulating NETosis: Increasing pH Promotes NADPH Oxidase-Dependent NETosis Khan, Meraj A. Philip, Lijy M. Cheung, Guillaume Vadakepeedika, Shawn Grasemann, Hartmut Sweezey, Neil Palaniyar, Nades Front Med (Lausanne) Medicine Neutrophils migrating from the blood (pH 7.35–7.45) into the surrounding tissues encounter changes in extracellular pH (pH(e)) conditions. Upon activation of NADPH oxidase 2 (Nox), neutrophils generate large amounts of H(+) ions reducing the intracellular pH (pH(i)). Nevertheless, how extracellular pH regulates neutrophil extracellular trap (NET) formation (NETosis) is not clearly established. We hypothesized that increasing pH increases Nox-mediated production of reactive oxygen species (ROS) and neutrophil protease activity, stimulating NETosis. Here, we found that raising pH(e) (ranging from 6.6 to 7.8; every 0.2 units) increased pH(i) of both activated and resting neutrophils within 10–20 min (Seminaphtharhodafluor dual fluorescence measurements). Since Nox activity generates H(+) ions, pH(i) is lower in neutrophils that are activated compared to resting. We also found that higher pH stimulated Nox-dependent ROS production (R123 generation; flow cytometry, plate reader assay, and imaging) during spontaneous and phorbol myristate acetate-induced NETosis (Sytox Green assays, immunoconfocal microscopy, and quantifying NETs). In neutrophils that are activated and not resting, higher pH stimulated histone H4 cleavage (Western blots) and NETosis. Raising pH increased Escherichia coli lipopolysaccharide-, Pseudomonas aeruginosa (Gram-negative)-, and Staphylococcus aureus (Gram-positive)-induced NETosis. Thus, higher pH(e) promoted Nox-dependent ROS production, protease activity, and NETosis; lower pH has the opposite effect. These studies provided mechanistic steps of pH(e)-mediated regulation of Nox-dependent NETosis. Raising pH either by sodium bicarbonate or Tris base (clinically known as Tris hydroxymethyl aminomethane, tromethamine, or THAM) increases NETosis. Each Tris molecule can bind 3H(+) ions, whereas each bicarbonate HCO3(−) ion binds 1H(+) ion. Therefore, the amount of Tris solution required to cause the same increase in pH level is less than that of equimolar bicarbonate solution. For that reason, regulating NETosis by pH with specific buffers such as THAM could be more effective than bicarbonate in managing NET-related diseases. Frontiers Media S.A. 2018-02-13 /pmc/articles/PMC5816902/ /pubmed/29487850 http://dx.doi.org/10.3389/fmed.2018.00019 Text en Copyright © 2018 Khan, Philip, Cheung, Vadakepeedika, Grasemann, Sweezey and Palaniyar. http://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 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 Medicine
Khan, Meraj A.
Philip, Lijy M.
Cheung, Guillaume
Vadakepeedika, Shawn
Grasemann, Hartmut
Sweezey, Neil
Palaniyar, Nades
Regulating NETosis: Increasing pH Promotes NADPH Oxidase-Dependent NETosis
title Regulating NETosis: Increasing pH Promotes NADPH Oxidase-Dependent NETosis
title_full Regulating NETosis: Increasing pH Promotes NADPH Oxidase-Dependent NETosis
title_fullStr Regulating NETosis: Increasing pH Promotes NADPH Oxidase-Dependent NETosis
title_full_unstemmed Regulating NETosis: Increasing pH Promotes NADPH Oxidase-Dependent NETosis
title_short Regulating NETosis: Increasing pH Promotes NADPH Oxidase-Dependent NETosis
title_sort regulating netosis: increasing ph promotes nadph oxidase-dependent netosis
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816902/
https://www.ncbi.nlm.nih.gov/pubmed/29487850
http://dx.doi.org/10.3389/fmed.2018.00019
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