Consequences of the constitutive NOX2 activity in living cells: Cytosol acidification, apoptosis, and localized lipid peroxidation

The phagocyte NADPH oxidase (NOX2) is a key enzyme of the innate immune system generating superoxide anions (O2•-), precursors of reactive oxygen species. The NOX2 protein complex is composed of six subunits: two membrane proteins (gp91phox and p22phox) forming the catalytic core, three cytosolic pr...

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Published inBiochimica et biophysica acta. Molecular cell research Vol. 1869; no. 9; p. 119276
Main Authors Valenta, Hana, Dupré-Crochet, Sophie, Abdesselem, Mouna, Bizouarn, Tania, Baciou, Laura, Nüsse, Oliver, Deniset-Besseau, Ariane, Erard, Marie
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.09.2022
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Abstract The phagocyte NADPH oxidase (NOX2) is a key enzyme of the innate immune system generating superoxide anions (O2•-), precursors of reactive oxygen species. The NOX2 protein complex is composed of six subunits: two membrane proteins (gp91phox and p22phox) forming the catalytic core, three cytosolic proteins (p67phox, p47phox and p40phox) and a small GTPase Rac. The sophisticated activation mechanism of the NADPH oxidase relies on the assembly of cytosolic subunits with the membrane-bound components. A chimeric protein, called ‘Trimera’, composed of the essential domains of the cytosolic proteins p47phox (aa 1–286), p67phox (aa 1–212) and full-length Rac1Q61L, enables a constitutive and robust NOX2 activity in cells without the need of any stimulus. We employed Trimera as a single activating protein of the phagocyte NADPH oxidase in living cells and examined the consequences on the cell physiology of this continuous and long-term NOX activity. We showed that the sustained high level of NOX activity causes acidification of the intracellular pH, triggers apoptosis and leads to local peroxidation of lipids in the membrane. These local damages to the membrane correlate with the strong tendency of the Trimera to clusterize in the plasma membrane observed by FRET-FLIM microscopy. •Trimera is a tool to trigger a continuous ROS production in living cells.•Continuous NOX2 activity causes cytosol acidification and apoptosis.•ROS overproduction leads to localized oxidation of the membrane lipids.•Trimera tends to clusterize in the plasma membrane of COSNOX and COS-7 cells.
AbstractList The phagocyte NADPH oxidase (NOX2) is a key enzyme of the innate immune system generating superoxide anions (O ), precursors of reactive oxygen species. The NOX2 protein complex is composed of six subunits: two membrane proteins (gp91 and p22 ) forming the catalytic core, three cytosolic proteins (p67 , p47 and p40 ) and a small GTPase Rac. The sophisticated activation mechanism of the NADPH oxidase relies on the assembly of cytosolic subunits with the membrane-bound components. A chimeric protein, called 'Trimera', composed of the essential domains of the cytosolic proteins p47 (aa 1-286), p67 (aa 1-212) and full-length Rac1Q61L, enables a constitutive and robust NOX2 activity in cells without the need of any stimulus. We employed Trimera as a single activating protein of the phagocyte NADPH oxidase in living cells and examined the consequences on the cell physiology of this continuous and long-term NOX activity. We showed that the sustained high level of NOX activity causes acidification of the intracellular pH, triggers apoptosis and leads to local peroxidation of lipids in the membrane. These local damages to the membrane correlate with the strong tendency of the Trimera to clusterize in the plasma membrane observed by FRET-FLIM microscopy.
The phagocyte NADPH oxidase (NOX2) is a key enzyme of the innate immune system generating superoxide anions (O2•-), precursors of reactive oxygen species. The NOX2 protein complex is composed of six subunits: two membrane proteins (gp91phox and p22phox) forming the catalytic core, three cytosolic proteins (p67phox, p47phox and p40phox) and a small GTPase Rac. The sophisticated activation mechanism of the NADPH oxidase relies on the assembly of cytosolic subunits with the membrane-bound components. A chimeric protein, called ‘Trimera’, composed of the essential domains of the cytosolic proteins p47phox (aa 1–286), p67phox (aa 1–212) and full-length Rac1Q61L, enables a constitutive and robust NOX2 activity in cells without the need of any stimulus. We employed Trimera as a single activating protein of the phagocyte NADPH oxidase in living cells and examined the consequences on the cell physiology of this continuous and long-term NOX activity. We showed that the sustained high level of NOX activity causes acidification of the intracellular pH, triggers apoptosis and leads to local peroxidation of lipids in the membrane. These local damages to the membrane correlate with the strong tendency of the Trimera to clusterize in the plasma membrane observed by FRET-FLIM microscopy. •Trimera is a tool to trigger a continuous ROS production in living cells.•Continuous NOX2 activity causes cytosol acidification and apoptosis.•ROS overproduction leads to localized oxidation of the membrane lipids.•Trimera tends to clusterize in the plasma membrane of COSNOX and COS-7 cells.
ArticleNumber 119276
Author Nüsse, Oliver
Erard, Marie
Baciou, Laura
Valenta, Hana
Abdesselem, Mouna
Bizouarn, Tania
Dupré-Crochet, Sophie
Deniset-Besseau, Ariane
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crossref_primary_10_1161_HYPERTENSIONAHA_123_19434
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Keywords aa
NADPH
Oxidative stress
PMA
NMDG
HRP
AFM
Lipid peroxidation
IR
FLIM
FP
FRET-FLIM
ROI
Intracellular pH
NADPH oxidase
ROS
FRET
DPI
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Snippet The phagocyte NADPH oxidase (NOX2) is a key enzyme of the innate immune system generating superoxide anions (O2•-), precursors of reactive oxygen species. The...
The phagocyte NADPH oxidase (NOX2) is a key enzyme of the innate immune system generating superoxide anions (O ), precursors of reactive oxygen species. The...
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StartPage 119276
SubjectTerms Cellular Biology
FRET-FLIM
Intracellular pH
Life Sciences
Lipid peroxidation
NADPH oxidase
Oxidative stress
ROS
Title Consequences of the constitutive NOX2 activity in living cells: Cytosol acidification, apoptosis, and localized lipid peroxidation
URI https://dx.doi.org/10.1016/j.bbamcr.2022.119276
https://www.ncbi.nlm.nih.gov/pubmed/35489654
https://search.proquest.com/docview/2658228531
https://hal.science/hal-03858717
Volume 1869
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