ROS Production by a Single Neutrophil Cell and Neutrophil Population upon Bacterial Stimulation

The reactive oxygen species (ROS) production by a single neutrophil after stimulation with S. aureus and E. coli was estimated by an electrochemical amperometric method with a high time resolution. This showed significant variability in the response of a single neutrophil to bacterial stimulation, f...

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Published inBiomedicines Vol. 11; no. 5; p. 1361
Main Authors Pleskova, Svetlana N., Erofeev, Alexander S., Vaneev, Alexander N., Gorelkin, Petr V., Bobyk, Sergey Z., Kolmogorov, Vasilii S., Bezrukov, Nikolay A., Lazarenko, Ekaterina V.
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LanguageEnglish
Published Switzerland MDPI AG 04.05.2023
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Abstract The reactive oxygen species (ROS) production by a single neutrophil after stimulation with S. aureus and E. coli was estimated by an electrochemical amperometric method with a high time resolution. This showed significant variability in the response of a single neutrophil to bacterial stimulation, from a “silent cell” to a pronounced response manifested by a series of chronoamperometric spikes. The amount of ROS produced by a single neutrophil under the influence of S. aureus was 5.5-fold greater than that produced under the influence of E. coli. The response of a neutrophil granulocyte population to bacterial stimulation was analyzed using luminol-dependent biochemiluminescence (BCL). The stimulation of neutrophils with S. aureus, as compared to stimulation with E. coli, caused a total response in terms of ROS production that was seven-fold greater in terms of the integral value of the light sum and 13-fold greater in terms of the maximum peak value. The method of ROS detection at the level of a single cell indicated the functional heterogeneity of the neutrophil population, but the specificity of the cellular response to different pathogens was the same at the cellular and population levels.
AbstractList The reactive oxygen species (ROS) production by a single neutrophil after stimulation with S. aureus and E. coli was estimated by an electrochemical amperometric method with a high time resolution. This showed significant variability in the response of a single neutrophil to bacterial stimulation, from a “silent cell” to a pronounced response manifested by a series of chronoamperometric spikes. The amount of ROS produced by a single neutrophil under the influence of S. aureus was 5.5-fold greater than that produced under the influence of E. coli. The response of a neutrophil granulocyte population to bacterial stimulation was analyzed using luminol-dependent biochemiluminescence (BCL). The stimulation of neutrophils with S. aureus, as compared to stimulation with E. coli, caused a total response in terms of ROS production that was seven-fold greater in terms of the integral value of the light sum and 13-fold greater in terms of the maximum peak value. The method of ROS detection at the level of a single cell indicated the functional heterogeneity of the neutrophil population, but the specificity of the cellular response to different pathogens was the same at the cellular and population levels.
The reactive oxygen species (ROS) production by a single neutrophil after stimulation with and was estimated by an electrochemical amperometric method with a high time resolution. This showed significant variability in the response of a single neutrophil to bacterial stimulation, from a "silent cell" to a pronounced response manifested by a series of chronoamperometric spikes. The amount of ROS produced by a single neutrophil under the influence of was 5.5-fold greater than that produced under the influence of . The response of a neutrophil granulocyte population to bacterial stimulation was analyzed using luminol-dependent biochemiluminescence (BCL). The stimulation of neutrophils with , as compared to stimulation with , caused a total response in terms of ROS production that was seven-fold greater in terms of the integral value of the light sum and 13-fold greater in terms of the maximum peak value. The method of ROS detection at the level of a single cell indicated the functional heterogeneity of the neutrophil population, but the specificity of the cellular response to different pathogens was the same at the cellular and population levels.
The reactive oxygen species (ROS) production by a single neutrophil after stimulation with S. aureus and E. coli was estimated by an electrochemical amperometric method with a high time resolution. This showed significant variability in the response of a single neutrophil to bacterial stimulation, from a “silent cell” to a pronounced response manifested by a series of chronoamperometric spikes. The amount of ROS produced by a single neutrophil under the influence of S. aureus was 5.5-fold greater than that produced under the influence of E. coli . The response of a neutrophil granulocyte population to bacterial stimulation was analyzed using luminol-dependent biochemiluminescence (BCL). The stimulation of neutrophils with S. aureus , as compared to stimulation with E. coli , caused a total response in terms of ROS production that was seven-fold greater in terms of the integral value of the light sum and 13-fold greater in terms of the maximum peak value. The method of ROS detection at the level of a single cell indicated the functional heterogeneity of the neutrophil population, but the specificity of the cellular response to different pathogens was the same at the cellular and population levels.
The reactive oxygen species (ROS) production by a single neutrophil after stimulation with S. aureus and E. coli was estimated by an electrochemical amperometric method with a high time resolution. This showed significant variability in the response of a single neutrophil to bacterial stimulation, from a "silent cell" to a pronounced response manifested by a series of chronoamperometric spikes. The amount of ROS produced by a single neutrophil under the influence of S. aureus was 5.5-fold greater than that produced under the influence of E. coli. The response of a neutrophil granulocyte population to bacterial stimulation was analyzed using luminol-dependent biochemiluminescence (BCL). The stimulation of neutrophils with S. aureus, as compared to stimulation with E. coli, caused a total response in terms of ROS production that was seven-fold greater in terms of the integral value of the light sum and 13-fold greater in terms of the maximum peak value. The method of ROS detection at the level of a single cell indicated the functional heterogeneity of the neutrophil population, but the specificity of the cellular response to different pathogens was the same at the cellular and population levels.The reactive oxygen species (ROS) production by a single neutrophil after stimulation with S. aureus and E. coli was estimated by an electrochemical amperometric method with a high time resolution. This showed significant variability in the response of a single neutrophil to bacterial stimulation, from a "silent cell" to a pronounced response manifested by a series of chronoamperometric spikes. The amount of ROS produced by a single neutrophil under the influence of S. aureus was 5.5-fold greater than that produced under the influence of E. coli. The response of a neutrophil granulocyte population to bacterial stimulation was analyzed using luminol-dependent biochemiluminescence (BCL). The stimulation of neutrophils with S. aureus, as compared to stimulation with E. coli, caused a total response in terms of ROS production that was seven-fold greater in terms of the integral value of the light sum and 13-fold greater in terms of the maximum peak value. The method of ROS detection at the level of a single cell indicated the functional heterogeneity of the neutrophil population, but the specificity of the cellular response to different pathogens was the same at the cellular and population levels.
Audience Academic
Author Erofeev, Alexander S.
Gorelkin, Petr V.
Bezrukov, Nikolay A.
Bobyk, Sergey Z.
Pleskova, Svetlana N.
Vaneev, Alexander N.
Kolmogorov, Vasilii S.
Lazarenko, Ekaterina V.
AuthorAffiliation 3 Laboratory of Biophysics, National University of Science and Technology MISIS, Leninskiy Prospect, 4, 119049 Moscow, Russia
1 Laboratory of Scanning Probe Microscopy, Lobachevsky State University of Nizhny Novgorod, 603950 Nizhny Novgorod, Russia
4 Chemistry Department, Lomonosov Moscow State University, Leninskie Gory 1-3, 119991 Moscow, Russia
2 Department “Nanotechnology and Biotechnology”, R.E. Alekseev Technical State University of Nizhny Novgorod, 603155 Nizhny Novgorod, Russia
AuthorAffiliation_xml – name: 3 Laboratory of Biophysics, National University of Science and Technology MISIS, Leninskiy Prospect, 4, 119049 Moscow, Russia
– name: 4 Chemistry Department, Lomonosov Moscow State University, Leninskie Gory 1-3, 119991 Moscow, Russia
– name: 1 Laboratory of Scanning Probe Microscopy, Lobachevsky State University of Nizhny Novgorod, 603950 Nizhny Novgorod, Russia
– name: 2 Department “Nanotechnology and Biotechnology”, R.E. Alekseev Technical State University of Nizhny Novgorod, 603155 Nizhny Novgorod, Russia
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/37239032$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1007/978-3-030-40406-2_9
10.1172/JCI37223
10.1084/jem.20161621
10.1021/jacs.9b01217
10.4049/jimmunol.1900235
10.17843/rpmesp.2019.361.4026
10.3390/jcm9030872
10.1128/JVI.73.2.1447-1452.1999
10.1016/j.injury.2020.11.018
10.1182/blood-2012-04-421040
10.1182/blood-2015-03-631572
10.1093/carcin/bgh046
10.1016/j.ccr.2009.06.017
10.1039/C8AY01339J
10.3390/nano13060963
10.1016/j.redox.2015.09.005
10.1093/cvr/cvw024
10.1016/j.bcp.2016.04.014
10.1007/s00441-017-2780-z
10.1016/j.immuni.2004.07.006
10.1186/s12951-019-0460-8
10.1002/cbic.200700746
10.1111/1574-6976.12057
10.1016/j.freeradbiomed.2010.09.016
10.1002/jlb.67.3.396
10.1002/jlb.59.2.270
10.1038/ni.2194
10.1186/s12974-018-1363-6
10.1128/IAI.73.11.7613-7619.2005
10.1093/rheumatology/ker520
10.1265/jjh.66.533
10.1126/science.aal5081
10.15789/1563-0625-2019-6-
10.1093/carcin/18.3.569
10.3390/jcm11082174
10.1021/acs.analchem.0c01256
10.1002/anie.201902734
10.3390/vaccines10101648
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Issue 5
Keywords S. aureus
neutrophil heterogeneity
luminol-dependent chemiluminescence
ROS production
electrochemical detection
neutrophils
E. coli
nanoelectrodes
Language English
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References ref_14
Christoffersson (ref_12) 2012; 120
Cheung (ref_43) 2014; 38
Hadley (ref_42) 2005; 73
Christoffersson (ref_6) 2018; 371
Amatore (ref_28) 2008; 9
Massena (ref_15) 2015; 126
Fridlender (ref_9) 2009; 16
(ref_2) 2019; 36
Saprykin (ref_17) 2001; 120
Valenta (ref_21) 2020; 1246
Zhang (ref_22) 2018; 10
Arbault (ref_26) 1997; 18
Dahlgren (ref_34) 2019; 202
Bylund (ref_37) 2010; 49
Abakumova (ref_10) 2020; 21
Lachgar (ref_25) 1999; 73
Dahlgren (ref_36) 2016; 114
Gerasimov (ref_20) 2001; 43
ref_24
Hu (ref_29) 2019; 141
ref_23
Lundqvist (ref_39) 1996; 59
ref_41
ref_40
Arbault (ref_27) 2004; 25
Zhang (ref_30) 2019; 58
Barnes (ref_4) 2012; 51
ref_3
Deniset (ref_8) 2017; 214
Alvarez (ref_35) 2015; 6
Teuben (ref_16) 2020; 52
Karlsson (ref_38) 2000; 67
Umeda (ref_1) 2011; 66
Vaneev (ref_31) 2020; 92
Jablonska (ref_13) 2010; 120
Obraztsov (ref_32) 2015; 9
Puga (ref_7) 2011; 13
Pleskova (ref_33) 2018; 60
Pleskova (ref_18) 2009; 135
Tsuda (ref_19) 2004; 21
ref_5
Ma (ref_11) 2016; 110
References_xml – volume: 1246
  start-page: 153
  year: 2020
  ident: ref_21
  article-title: The NADPH Oxidase and the Phagosome
  publication-title: Adv. Exp. Med. Biol.
  doi: 10.1007/978-3-030-40406-2_9
– volume: 120
  start-page: 1151
  year: 2010
  ident: ref_13
  article-title: Neutrophils responsive to endogenous IFN-beta regulate tumor angiogenesis and growth in a mouse tumor model
  publication-title: J. Clin. Investig.
  doi: 10.1172/JCI37223
– volume: 214
  start-page: 1333
  year: 2017
  ident: ref_8
  article-title: Splenic Ly6G high mature and Ly6Gint immature neutrophils contribute to eradication of S. pneumoniae
  publication-title: J. Exp. Med.
  doi: 10.1084/jem.20161621
– volume: 141
  start-page: 4564
  year: 2019
  ident: ref_29
  article-title: Electrochemical measurements of reactive oxygen and nitrogen species inside single phagolysosomes of living macrophages
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.9b01217
– volume: 202
  start-page: 3127
  year: 2019
  ident: ref_34
  article-title: Intracellular neutrophil oxidants: From laboratory curiosity to clinical reality
  publication-title: J. Immunol.
  doi: 10.4049/jimmunol.1900235
– volume: 36
  start-page: 54
  year: 2019
  ident: ref_2
  article-title: Adrenergic and cholinergic influence on the production of reactive oxygen species in human neutrophils
  publication-title: Rev. Peru. Med. Exp. Salud Publica
  doi: 10.17843/rpmesp.2019.361.4026
– ident: ref_3
  doi: 10.3390/jcm9030872
– volume: 73
  start-page: 1447
  year: 1999
  ident: ref_25
  article-title: Amplification of the inflammatory cellular redox state by human immunodeficiency virus type 1-immunosuppressive tat and gp160 proteins
  publication-title: J. Virol.
  doi: 10.1128/JVI.73.2.1447-1452.1999
– volume: 52
  start-page: 426
  year: 2020
  ident: ref_16
  article-title: Instant intra-operative neutropenia despite the emergence of banded (CD16 dim/CD62L bright) neutrophils in peripheral blood—An observational study during extensive trauma-surgery in pigs
  publication-title: Injury
  doi: 10.1016/j.injury.2020.11.018
– volume: 120
  start-page: 4653
  year: 2012
  ident: ref_12
  article-title: VEGF-A recruits a proangiogenic MMP-9-delivering neutrophil subset that induces angiogenesis in transplanted hypoxic tissue
  publication-title: Blood
  doi: 10.1182/blood-2012-04-421040
– volume: 126
  start-page: 2016
  year: 2015
  ident: ref_15
  article-title: Identification and characterization of VEGF-A-responsive neutrophils expressing CD49d, VEGFR1, and CXCR4 in mice and humans
  publication-title: Blood
  doi: 10.1182/blood-2015-03-631572
– volume: 25
  start-page: 509
  year: 2004
  ident: ref_27
  article-title: Oxidative stress in cancer prone xeroderma pigmentosumfibroblasts. Real-time and single cell monitoring of superoxide and nitric oxide production with microelectrodes
  publication-title: Carcinogenesis
  doi: 10.1093/carcin/bgh046
– volume: 16
  start-page: 183
  year: 2009
  ident: ref_9
  article-title: Polarization of tumor-associated neutrophil phenotype by TGF-beta: «BN1» versus «BN2» TAN
  publication-title: Cancer Cell
  doi: 10.1016/j.ccr.2009.06.017
– volume: 10
  start-page: 4625
  year: 2018
  ident: ref_22
  article-title: Methods for the detection of reactive oxygen species
  publication-title: Anal. Methods
  doi: 10.1039/C8AY01339J
– ident: ref_23
  doi: 10.3390/nano13060963
– volume: 6
  start-page: 472
  year: 2015
  ident: ref_35
  article-title: Reactive oxygen species and mitochondria: A nexus of cellular homeostasis
  publication-title: Redox. Biol.
  doi: 10.1016/j.redox.2015.09.005
– volume: 110
  start-page: 51
  year: 2016
  ident: ref_11
  article-title: Temporal neutrophil polarization following myocardial infarction
  publication-title: Cardiovasc. Res.
  doi: 10.1093/cvr/cvw024
– volume: 60
  start-page: 623
  year: 2018
  ident: ref_33
  article-title: Features of phagocytosis of opsonized and nonopsonized bacteria Staphylococcus aureus and Escherichia coli by human neutrophil granulocytes, studied by atomic force microscopy
  publication-title: Cell Tissue Biol.
– volume: 9
  start-page: 418
  year: 2015
  ident: ref_32
  article-title: Evaluation of the func-tional activity of whole blood neutrophils by a two stage stimulation: A new approach to the chemiluminescent analysis
  publication-title: Russ. J. Immunol.
– volume: 114
  start-page: 22
  year: 2016
  ident: ref_36
  article-title: Basic characteristics of the neutrophil receptors that recognize formylated peptides, a danger-associated molecular pattern generated by bacteria and mitochondria
  publication-title: Biochem. Pharmacol.
  doi: 10.1016/j.bcp.2016.04.014
– volume: 371
  start-page: 415
  year: 2018
  ident: ref_6
  article-title: The neutrophil: One cell on many missions or many cells with different agendas?
  publication-title: Cell Tissue Res.
  doi: 10.1007/s00441-017-2780-z
– volume: 21
  start-page: 215
  year: 2004
  ident: ref_19
  article-title: Three different neutrophil subsets exhibited in mice with different susceptibilities to infection by methicillin-resistant Staphylococcus aureus
  publication-title: Immunity
  doi: 10.1016/j.immuni.2004.07.006
– ident: ref_24
  doi: 10.1186/s12951-019-0460-8
– volume: 9
  start-page: 1472
  year: 2008
  ident: ref_28
  article-title: Real-time amperometric analysis of reactive oxygen and nitrogen species released by single immunostimulated macrophages
  publication-title: Chembiochem
  doi: 10.1002/cbic.200700746
– volume: 38
  start-page: 698
  year: 2014
  ident: ref_43
  article-title: Phenol-soluble modulins—Critical determinants of staphylococcal viru-lence
  publication-title: FEMS Microbiol. Rev.
  doi: 10.1111/1574-6976.12057
– volume: 49
  start-page: 1834
  year: 2010
  ident: ref_37
  article-title: Intracellular generation of superoxide by the phagocyte NADPH oxidase: How, where, and what for?
  publication-title: Free Radic. Biol. Med.
  doi: 10.1016/j.freeradbiomed.2010.09.016
– volume: 67
  start-page: 396
  year: 2000
  ident: ref_38
  article-title: Phorbol myristate acetate induces neutrophil NADPH-oxidase activity by two separate signal transduction pathways: Dependent or independent of phosphatidylinositol 3-kinase
  publication-title: J. Leukoc. Biol.
  doi: 10.1002/jlb.67.3.396
– volume: 59
  start-page: 270
  year: 1996
  ident: ref_39
  article-title: Phorbol myristate acetate-induced NADPH oxidase activity in human neutrophils: Only half the story has been told
  publication-title: J. Leukoc. Biol.
  doi: 10.1002/jlb.59.2.270
– volume: 13
  start-page: 170
  year: 2011
  ident: ref_7
  article-title: B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen
  publication-title: Nat. Immunol.
  doi: 10.1038/ni.2194
– ident: ref_41
  doi: 10.1186/s12974-018-1363-6
– volume: 73
  start-page: 7613
  year: 2005
  ident: ref_42
  article-title: Peptidoglycan of Staphylococcus aureus upregulates monocyte expression of CD14, toll-like receptor 2 (TLR2), and TLR4 in human blood: Possible implications for riming of lipopolysac-charide signaling
  publication-title: Infect. Immun.
  doi: 10.1128/IAI.73.11.7613-7619.2005
– volume: 51
  start-page: 1166
  year: 2012
  ident: ref_4
  article-title: Neutrophil-derived reactive oxygen species in SSc
  publication-title: Rheumatology
  doi: 10.1093/rheumatology/ker520
– volume: 120
  start-page: 37
  year: 2001
  ident: ref_17
  article-title: Morphological variants of neutrophilic granulocytes in the blood of practically normal humans
  publication-title: Morphologiia
– volume: 66
  start-page: 533
  year: 2011
  ident: ref_1
  article-title: Changes in neutrophil immune functions under different exercise stresses
  publication-title: Nihon Eiseigaku Zasshi.
  doi: 10.1265/jjh.66.533
– ident: ref_14
  doi: 10.1126/science.aal5081
– volume: 43
  start-page: 432
  year: 2001
  ident: ref_20
  article-title: Functional heterogenicity of human blood neutrophils: Generation of oxygen active species
  publication-title: Tsitologiia
– volume: 21
  start-page: 1127
  year: 2020
  ident: ref_10
  article-title: Phenotype of circulating neutrophils at different stages of cervical neoplasia
  publication-title: Med. Immunol.
  doi: 10.15789/1563-0625-2019-6-
– volume: 135
  start-page: 47
  year: 2009
  ident: ref_18
  article-title: Differences in the functional activity of human neutrophilic granulocytes in their interactions with semiconductor quantum dots
  publication-title: Morphologiia
– volume: 18
  start-page: 569
  year: 1997
  ident: ref_26
  article-title: Activation of the NADPH oxidase in human fibroblasts by mechanical intrusion of a single cell with an ultramicroelectrode
  publication-title: Carcinogenesis
  doi: 10.1093/carcin/18.3.569
– ident: ref_5
  doi: 10.3390/jcm11082174
– volume: 92
  start-page: 8010
  year: 2020
  ident: ref_31
  article-title: In vitro and in vivo electrochemical measurement of reactive oxygen species after treatment with anticancer drugs
  publication-title: Anal. Chem.
  doi: 10.1021/acs.analchem.0c01256
– volume: 58
  start-page: 7753
  year: 2019
  ident: ref_30
  article-title: lectrochemical monitoring of ROS/RNS homeostasis within individual phagolysosomes inside single macrophages
  publication-title: Angew. Chem. Int. Ed. Engl.
  doi: 10.1002/anie.201902734
– ident: ref_40
  doi: 10.3390/vaccines10101648
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Snippet The reactive oxygen species (ROS) production by a single neutrophil after stimulation with S. aureus and E. coli was estimated by an electrochemical...
The reactive oxygen species (ROS) production by a single neutrophil after stimulation with and was estimated by an electrochemical amperometric method with a...
The reactive oxygen species (ROS) production by a single neutrophil after stimulation with S. aureus and E. coli was estimated by an electrochemical...
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StartPage 1361
SubjectTerms Analysis
B cells
Bacteria
Carbon
Cytochrome
Cytoplasm
E coli
electrochemical detection
Electrodes
Escherichia coli
Fibroblasts
Genotype & phenotype
Leukocytes (granulocytic)
Leukocytes (neutrophilic)
Methods
Morphology
neutrophil heterogeneity
Neutrophils
Population levels
Quantum dots
Reactive oxygen species
ROS production
S. aureus
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Title ROS Production by a Single Neutrophil Cell and Neutrophil Population upon Bacterial Stimulation
URI https://www.ncbi.nlm.nih.gov/pubmed/37239032
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Volume 11
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