Evidence map›Paper›PMID 31650185›Full record

ArticleCellular and molecular life sciences : CMLS2020

Nitric oxide and peroxynitrite trigger and enhance release of neutrophil extracellular traps.

Aneta Manda-Handzlik, Weronika Bystrzycka, Adrianna Cieloch, Eliza Glodkowska-Mrowka, Ewa Jankowska-Steifer, Edyta Heropolitanska-Pliszka, Agnieszka Skrobot, Angelika Muchowicz, Olga Ciepiela, Malgorzata Wachowska and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
2.8field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

49 citing papers in PubMed, 71 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Aneta Manda-HandzlikDepartment of Laboratory Medicine and Clinical Immunology of Developmental Age, Medical University of Warsaw, Zwirki i Wigury 63a Street, 02-091, Warsaw, Poland.ORCID http://orcid.org/0000-0002-3766-5466
Weronika BystrzyckaDepartment of Laboratory Medicine and Clinical Immunology of Developmental Age, Medical University of Warsaw, Zwirki i Wigury 63a Street, 02-091, Warsaw, Poland.ORCID http://orcid.org/0000-0003-3036-9864
Adrianna CielochDepartment of Laboratory Medicine and Clinical Immunology of Developmental Age, Medical University of Warsaw, Zwirki i Wigury 63a Street, 02-091, Warsaw, Poland.
Eliza Glodkowska-MrowkaDepartment of Laboratory Medicine and Clinical Immunology of Developmental Age, Medical University of Warsaw, Zwirki i Wigury 63a Street, 02-091, Warsaw, Poland.ORCID http://orcid.org/0000-0002-5865-8425
Ewa Jankowska-SteiferDepartment of Histology and Embryology, Medical University of Warsaw, Chalubinskiego 5 Street, 02-004, Warsaw, Poland.ORCID http://orcid.org/0000-0002-3868-5821
Edyta Heropolitanska-PliszkaDepartment of Immunology, The Children's Memorial Health Institute, Aleja Dzieci Polskich 20, 04-730, Warsaw, Poland.ORCID http://orcid.org/0000-0001-5519-2730
Agnieszka SkrobotDepartment of Laboratory Medicine and Clinical Immunology of Developmental Age, Medical University of Warsaw, Zwirki i Wigury 63a Street, 02-091, Warsaw, Poland.ORCID http://orcid.org/0000-0002-2346-2633
Angelika MuchowiczDepartment of Immunology, Medical University of Warsaw, Jana Nielubowicza 5 Street, 02-097, Warsaw, Poland.ORCID http://orcid.org/0000-0003-4707-1722
Olga CiepielaDepartment of Laboratory Diagnostics, Medical University of Warsaw, Banacha 1a Street, 02-097, Warsaw, Poland.ORCID http://orcid.org/0000-0002-3694-4076
Malgorzata WachowskaDepartment of Laboratory Medicine and Clinical Immunology of Developmental Age, Medical University of Warsaw, Zwirki i Wigury 63a Street, 02-091, Warsaw, Poland. malgorzata.wachowska@wum.edu.pl.ORCID http://orcid.org/0000-0001-7199-9649
Urszula DemkowDepartment of Laboratory Medicine and Clinical Immunology of Developmental Age, Medical University of Warsaw, Zwirki i Wigury 63a Street, 02-091, Warsaw, Poland.ORCID http://orcid.org/0000-0003-0674-9824
Medical University of Warsaw · PLChildren's Memorial Health Institute · PLUniversity of Copenhagen · DK

Funding

Fundacja na rzecz Nauki Polskiej POWROTY/2016-2/7Fundacja na rzecz Nauki Polskiej START 2019Narodowe Centrum Nauki 2015/19/N/NZ6/01317
6 · The paper itself

Abstract

Despite great interest, the mechanism of neutrophil extracellular traps (NETs) release is not fully understood and some aspects of this process, e.g. the role of reactive nitrogen species (RNS), still remain unclear. Therefore, our aim was to investigate the mechanisms underlying RNS-induced formation of NETs and contribution of RNS to NETs release triggered by various physiological and synthetic stimuli. The involvement of RNS in NETs formation was studied in primary human neutrophils and differentiated human promyelocytic leukemia cells (HL-60 cells). RNS (peroxynitrite and nitric oxide) efficiently induced NETs release and potentiated NETs-inducing properties of platelet activating factor and lipopolysaccharide. RNS-induced NETs formation was independent of autophagy and histone citrullination, but dependent on the activity of phosphoinositide 3-kinases (PI3K) and myeloperoxidase, as well as selective degradation of histones H2A and H2B by neutrophil elastase. Additionally, NADPH oxidase activity was required to release NETs upon stimulation with NO, as shown in NADPH-deficient neutrophils isolated from patients with chronic granulomatous disease. The role of RNS was further supported by increased RNS synthesis upon stimulation of NETs release with phorbol 12-myristate 13-acetate and calcium ionophore A23187. Scavenging or inhibition of RNS formation diminished NETs release triggered by these stimuli while scavenging of peroxynitrite inhibited NO-induced NETs formation. Our data suggest that RNS may act as mediators and inducers of NETs release. These processes are PI3K-dependent and ROS-dependent. Since inflammatory reactions are often accompanied by nitrosative stress and NETs formation, our studies shed a new light on possible mechanisms engaged in various immune-mediated conditions.

Indexed as

AdenineDNAExtracellular TrapsGranulomatous Disease, ChronicHumansLeukocyte ElastaseNeutrophilsNitric Oxidep38 Mitogen-Activated Protein KinasesPeroxynitrous AcidPhosphatidylinositol 3-KinasesReactive Nitrogen SpeciesReactive Oxygen SpeciesSignal TransductionS-Nitroso-N-Acetylpenicillamine3-methyladenineAdenineDNALeukocyte ElastaseNitric Oxidep38 Mitogen-Activated Protein KinasesPeroxynitrous AcidPhosphatidylinositol 3-KinasesReactive Nitrogen SpeciesReactive Oxygen SpeciesS-Nitroso-N-AcetylpenicillamineAutophagyNeutrophil extracellular trapsNitric oxidePeroxynitritePhosphoinositide 3-kinasesReactive nitrogen species

Identifiers

PMID31650185
PMCPMC7366602
OpenAlexW2981324746

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.