Evidence map›Paper›PMID 38696730›Full record

ArticleG3 (Bethesda, Md.)2024

A nox2/cybb zebrafish mutant with defective myeloid cell reactive oxygen species production displays normal initial neutrophil recruitment to sterile tail injuries.

Abdulsalam I Isiaku, Zuobing Zhang, Vahid Pazhakh, Graham J Lieschke

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Abdulsalam I IsiakuAustralian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800, Australia.ORCID 0000-0002-8354-8674
Zuobing ZhangAustralian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800, Australia.
Vahid PazhakhAustralian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800, Australia.
Graham J LieschkeAustralian Regenerative Medicine Institute, Monash University, Clayton, VIC 3800, Australia.

Funding

Severe Chronic Neutropenia International RegistryR24AI049393 · NIAID · UNIVERSITY OF WASHINGTON · PI DALE, DAVID CHANDLER · 2004 to 2019
$10.6M
Severe Chronic Neutropenia International RegistryR24AI162637 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI PETER E NEWBURGER, Akiko Shimamura · 2022 to 2026
$5.8M
Australian GovernmentAustralian Research Council DP170102235China Scholarship Council 201608140011Graduate Scholarship and International Tuition ScholarshipMaddie Riewoldt'sMonash UniversityNational Health and Medical Research Council 1044754NIAID NIH HHS R24 AI049393NIAID NIH HHS R24 AI162637State Government of VictoriaVision ARMI-MRV-2018G
6 · The paper itself

Abstract

Reactive oxygen species are important effectors and modifiers of the acute inflammatory response, recruiting phagocytes including neutrophils to sites of tissue injury. In turn, phagocytes such as neutrophils are both consumers and producers of reactive oxygen species. Phagocytes including neutrophils generate reactive oxygen species in an oxidative burst through the activity of a multimeric phagocytic nicotinamide adenine dinucleotide phosphate oxidase complex. Mutations in the NOX2/CYBB (previously gp91phox) nicotinamide adenine dinucleotide phosphate oxidase subunit are the commonest cause of chronic granulomatous disease, a disease characterized by infection susceptibility and an inflammatory phenotype. To model chronic granulomatous disease, we made a nox2/cybb zebrafish (Danio rerio) mutant and demonstrated it to have severely impaired myeloid cell reactive oxygen species production. Reduced early survival of nox2 mutant embryos indicated an essential requirement for nox2 during early development. In nox2/cybb zebrafish mutants, the dynamics of initial neutrophil recruitment to both mild and severe surgical tailfin wounds was normal, suggesting that excessive neutrophil recruitment at the initiation of inflammation is not the primary cause of the "sterile" inflammatory phenotype of chronic granulomatous disease patients. This nox2 zebrafish mutant adds to existing in vivo models for studying reactive oxygen species function in myeloid cells including neutrophils in development and disease.

Indexed as

MutationMyeloid CellsNADPH Oxidase 2Reactive Oxygen SpeciesZebrafishAnimalsDisease Models, AnimalGranulomatous Disease, ChronicNADPH OxidasesNeutrophil InfiltrationNeutrophilsTailZebrafish ProteinsNADPH Oxidase 2NADPH OxidasesReactive Oxygen SpeciesZebrafish Proteinsacute inflammationchemotaxischronic granulomatous diseasecybbneutrophilsnox2ROSwoundzebrafish

Identifiers

PMID38696730
PMCPMC11152067

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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.