The DOI matches its Crossref record; 96 of the 99 references it cites were found in a registry or an index.
Zebrafish as a model for the study of neutrophil biology
Abstract
To understand inflammation and immunity, we need to understand the biology of the neutrophil. Whereas these cells can readily be extracted from peripheral blood, their short lifespan makes genetic manipulations impractical. Murine knockout models have been highly informative, and new imaging techniques are allowing neutrophils to be seen during inflammation in vivo for the first time. However, there is a place for a new model of neutrophil biology, which readily permits imaging of individual neutrophils during inflammation in vivo, combined with the ease of genetic and chemical manipulation. The zebrafish has long been the model of choice for the developmental biology community, and the availability of genomic resources and tools for gene manipulation makes this an attractive model. Zebrafish innate immunity shares many features with mammalian systems, including neutrophils with morphological, biochemical, and functional features, also shared with mammalian neutrophils. Transgenic zebrafish with neutrophils specifically labeled with fluorescent proteins have been generated, and this advance has led to the adoption of zebrafish, alongside existing models, by a number of groups around the world. The use of these models has underpinned a number of key advances in the field, including the identification of a tissue gradient of hydrogen peroxide for neutrophil recruitment following tissue injury and direct evidence for reverse migration as a regulatable mechanism of inflammation resolution. In this review, we discuss the importance of zebrafish models in neutrophil biology and describe how the understanding of neutrophil biology has been advanced by the use of these models.
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“These models offer unique possibilities, e.g., to perform live imaging, due to their translucency, and genome-wide screen, due to their good genetic tractability and low cost.”
From Transition from inflammation to proliferation: a critical step during wound healing (2016) · cites this paper as [267]
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“Recently, Drosophila and zebrafish are used to investigate mechanisms of fundamental tissue repair [267, 268].”
From Transition from inflammation to proliferation: a critical step during wound healing (2016) · cites this paper as [267]
In the citing paper
“Although they have their own limitations, Drosophila and zebrafish models offer translucency for live imaging and even greater genetic tractability than mice, to study fundamental tissue repair mechanisms not possible in humans.”
From Wound repair and regeneration: Mechanisms, signaling, and translation (2014) · cites this paper as [118]
Citations
Cites
Stages of embryonic development of the zebrafish
Kimmel, C. B., Ballard, W. W., Kimmel, S. R., Ullmann, B., & Schilling, T. F. (1995) · Developmental Dynamics · doi:10.1002/aja.1002030302 · Cited by 12,037
Effective targeted gene ‘knockdown’ in zebrafish
Nasevicius, A., & Ekker, S. C. (2000) · Nature Genetics · doi:10.1038/79951 · Cited by 2,485
Conditional gene targeting in macrophages and granulocytes using LysMcre mice
Clausen, B. E., Burkhardt, C., Reith, W., Renkawitz, R., & Förster, I. (1999) · Transgenic Research · doi:10.1023/a:1008942828960 · Cited by 2,098
Collins, S. J., Ruscetti, F. W., Gallagher, R. E., & Gallo, R. C. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.5.2458 · Cited by 1,594
Wang, Y., Li, M., Stadler, S. C., Correll, S., Li, P., Wang, D., Hayama, R., Leonelli, L., Han, H., Grigoryev, S. A., et al. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200806072 · Cited by 1,579
A tissue-scale gradient of hydrogen peroxide mediates rapid wound detection in zebrafish
Niethammer, P., Grabher, C., Look, A. T., & Mitchison, T. J. (2009) · Nature · doi:10.1038/nature08119 · Cited by 1,541
Savill, J. S., Wyllie, A. H., Henson, J. E., Walport, M. J., Henson, P. M., & Haslett, C. (1989) · Journal of Clinical Investigation · doi:10.1172/jci113970 · Cited by 1,536
Transparent Adult Zebrafish as a Tool for In Vivo Transplantation Analysis
White, R. M., Sessa, A., Burke, C., Bowman, T., LeBlanc, J., Ceol, C., Bourque, C., Dovey, M., Goessling, W., Burns, C. E., et al. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2007.11.002 · Cited by 1,408
Resolvin E1 and protectin D1 activate inflammation-resolution programmes
Schwab, J. M., Chiang, N., Arita, M., & Serhan, C. N. (2007) · Nature · doi:10.1038/nature05877 · Cited by 1,219
Intravascular Danger Signals Guide Neutrophils to Sites of Sterile Inflammation
McDonald, B., Pittman, K., Menezes, G. B., Hirota, S. A., Slaba, I., Waterhouse, C. C. M., Beck, P. L., Muruve, D. A., & Kubes, P. (2010) · Science · doi:10.1126/science.1195491 · Cited by 1,210
Research works printed but not linked: 1
- CC, R-A., K., H., SA, R, 2012, Proceedings, Medical Image Understanding and Analysis
Cited by
Sorted by citations
Items 101–143 of 143
Models for the Study of the Cross Talk Between Inflammation and Cell Cycle
Hoodless, L. J., Robb, C. T., Felton, J. M., Tucker, C. S., & Rossi, A. G. (2015) · Methods in molecular biology · doi:10.1007/978-1-4939-2926-9_15 · Cited by 7
Zatti, S. A., Arana, S., Maia, A. A. M., & Adriano, E. A. (2016) · Parasitology Research · doi:10.1007/s00436-016-5248-2 · Cited by 7
Zhang, W., Piao, L., & Liu, X. (2020) · Journal of Functional Foods · doi:10.1016/j.jff.2020.104216 · Cited by 8
Buchan, K. D., van Gent, M., Prajsnar, T. K., Ogryzko, N. V., de Jong, N. W. M., Kolata, J., Foster, S. J., van Strijp, J. A. G., & Renshaw, S. A. (2021) · Journal of Cell Science · doi:10.1242/jcs.252205 · Cited by 7
Self-citationLin, H., Saputra, F., Audira, G., Lai, Y., Roldan, M. J. M., Alos, H. C., Aventurado, C. A., Vasquez, R. D., Tsai, G.-J., Lim, K., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911711 · Cited by 6
Sarkar, P., & Arockiaraj, J. (2022) · International Journal of Peptide Research and Therapeutics · doi:10.1007/s10989-022-10471-5 · Cited by 5
Guan, R., Wen, X., Leung, C. H., Ciano‐Oliveira, C. D., Lam, S., Dai, S. Y., Karbassi, F., Mauro, A., Wang, Y., & Rotstein, O. D. (2021) · PLoS ONE · doi:10.1371/journal.pone.0260442 · Cited by 5
Darroch, H., Astin, J. W., & Hall, C. J. (2019) · Methods in molecular biology · doi:10.1007/978-1-0716-0154-9_5 · Cited by 5
Mechanical Vessel Injury in Zebrafish Embryos
Clay, H., & Coughlin, S. R. (2015) · Journal of Visualized Experiments · doi:10.3791/52460 · Cited by 5
Santos, M. D. F., Carneiro, W. F., Virote, B. D. C. R., da Silva, K. C. D., Castro, T. F. D., Coli, A., Murgas, L. D. S., Ferrante, M., Gavilanes, M. L., & Carvalho, E. E. N. (2023) · Oriental Pharmacy and Experimental Medicine · doi:10.1007/s13596-023-00722-1 · Cited by 4
Kwiatkowska, I., Hermanowicz, J. M., Czarnomysy, R., Surażyński, A., Kowalczuk, K., Kałafut, J., Przybyszewska-Podstawka, A., Bielawski, K., Rivero‐Müller, A., Mojzych, M., et al. (2023) · Cancers · doi:10.3390/cancers16010122 · Cited by 4
Metainflammation alters neutrophil function and migration in vivo in response to tissue injury
Michael, C., Cantón-Sandoval, J., Norberto, M. F., Scharf, P. R. D. S., & de Oliveira, S. (2025) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiaf094 · Cited by 4
Use of Larval Zebrafish Model to Study Within-Host Infection Dynamics
Prajsnar, T. K., McVicker, G., Williams, A., Renshaw, S. A., & Foster, S. J. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7638-6_14 · Cited by 4
Self-citationReal-time functional analysis of Hv1 channel in neutrophils: a new approach from zebrafish model
Ratanayotha, A., Kawai, T., & Okamura, Y. (2019) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00326.2018 · Cited by 4
Xu, H., Piao, L., Shen, X., & Liu, X. (2024) · Journal of Functional Foods · doi:10.1016/j.jff.2024.106017 · Cited by 4
Laux, D. W., Kelly, L., Bravo, I. R., Ramezani, T., & Feng, Y. (2016) · Methods in cell biology · doi:10.1016/bs.mcb.2016.10.002 · Cited by 4
Norberto, M. F., Michael, C., & de Oliveira, S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.03.462893 · Cited by 4
Dual-action fermented oats (Avena sativa L.): Anti-inflammatory and skin barrier restoration
Liu, M., Wang, L., Li, Y., Zhang, P., Wang, C., Wu, Y., Chen, Y., Huang, H., & Li, X. (2025) · Journal of Dermatologic Science and Cosmetic Technology · doi:10.1016/j.jdsct.2025.100103 · Cited by 3
Elie Metchnikoff: Father of phagocytosis theory and pioneer of experiments in vivo
Korzh, V. P., & Bregestovski, P. D. (2016) · Cytology and Genetics · doi:10.3103/s0095452716020080 · Cited by 3
Threonine dehydrogenase regulates neutrophil homeostasis but not H3K4me3 levels in zebrafish
Li, N., Wang, Z., Zhang, F., Feng, C., Chen, Y., Liu, D., Chen, S.-B., Jin, Y., Zhang, Y., Xie, Y., et al. (2024) · FEBS Journal · doi:10.1111/febs.17138 · Cited by 2
Li, R., Yu, Y., Cheng, W., Li, Q., Xu, W., Cheng, J., Tao, L., & Zhang, Y. (2025) · Journal of Environmental Management · doi:10.1016/j.jenvman.2025.126355 · Cited by 2
Mechanical Vessel Injury in Zebrafish Embryos
Clay, H., & Coughlin, S. R. (2015) · Journal of Visualized Experiments · doi:10.3791/52460-v · Cited by 2
MicroRNA-375 modulates neutrophil chemotaxis via targeting Cathepsin B in zebrafish
Wang, D., Wang, T., Kim, D. J., Tan, S., Liu, S., Wan, J., & Deng, Q. (2024) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2024.109933 · Cited by 1
Analysis of Vascular Morphogenesis in Zebrafish
Hubert, M., & Herzog, W. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-2887-4_24 · Cited by 1
Complement System Inhibitory Drugs in a Zebrafish (Danio rerio) Model: Computational Modeling
Fernandes, D. C., & Tambourgi, D. V. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241813895 · Cited by 1
Habenicht, L. M. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-812431-4.00020-8 · Cited by 1
Hif-1α stabilisation polarises macrophages via cyclooxygenase/prostaglandin E2 in vivoPreprint
Lewis, A., & Elks, P. M. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/536862 · Cited by 1
Buchan, K. D., van Gent, M., Prajsnar, T. K., Ogryzko, N. V., de Jong, N. W. M., Kolata, J., Foster, S. J., van Strijp, J. A. G., & Renshaw, S. A. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.18.955021 · Cited by 1
Self-citationAn arginase 2 promoter transgenic illuminates anti-inflammatory signalling in zebrafishPreprint
Hammond, F. R., Lewis, A., Anderson, H. E., Williams, L. G., Meijer, A. H., Wiegertjes, G. F., & Elks, P. M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.14.480079 · Cited by 1
Santos, M. D. F., da Silva, K. C. D., Carneiro, W. F., Castro, T. F. D., Virote, B. D. C. R., Murgas, L. D. S., Bertolucci, S. K. V., Ferrante, M., Gavilanes, M. L., & Carvalho, E. E. N. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4201198 · Cited by 1
(2014) · Inflammation and Cell Signaling · doi:10.14800/ics.318
Zhang, M., Zhang, W., Wen, Z., Yan, B., Han, P., Pan, L., Lü, W., & Xiong, J. (2014)
Moigne, V. L., Rodriguez-Rincon, D., Glatigny, S., Dupont, C., Langevin, C., Said, A. A. A., Renshaw, S. A., Floto, R. A., Herrmann, J., & Bernut, A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.30.454490
Self-citationMicrorna-375 Modulates Neutrophil Capacity Via Targeting Ctsba in ZebrafishPreprint
Deng, Q., Wang, D., Wang, T., Kim, D. J., Liu, S., & Wan, J. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4883741
Feng, H., Shu, Y., Tang, Q., Li, Y., Chen, Z., He, W., Yang, X., Cao, H., & Shao, M. (2025) · Journal of Functional Foods · doi:10.1016/j.jff.2025.107001
Candida spp. suppress neutrophil reactive nitrogen species to evade killing
Burgess, T. B., Hammond, F. R., Szkuta, P. T., Lewis, A., Christou, S., Bowden, K. A., Bicanic, T. A., Prince, L. R., Ayscough, K. R., Partridge, D. G., et al. (2026) · mBio · doi:10.1128/mbio.00202-26 · Cited by 1
Zhong, Y., Zhang, L., Deng, Y., Shao, Q., Liang, J., Jiang, G., & He, Q. (2026) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2026.122172
Zheng, Z., Tian, R., Chen, Y., Li, Y., Pan, T., & Pan, T. (2026) · Journal of Translational Medicine · doi:10.1186/s12967-026-08626-9
Wang, X., Du, P., Taneja, K., Doon‐Ralls, J., Reátegui, E., & Holland, M. A. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.21.746187
He, R., Li, C., Mao, X., Huang, C., Yang, M., Li, J., Wu, X., & Yang, L. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27177951
Neutrophils – Insights into innate cell responses using a zebrafish model
Marana, M. H., Mathiessen, H., & Jørgensen, L. V. G. (2026) · Fish physiology · doi:10.1016/bs.fp.2026.08.006
Metadata
- Authors
- Henry, K. M., Loynes, C. A., Whyte, M. K. B., & Renshaw, S. A.
- Affiliations
- Medical Research Council (GB)
- Corresponding author
- Renshaw, Stephen A
- Venue
- Journal of Leukocyte Biology
- Publisher
- Oxford University Press (OUP)
- Published
- 2013-10-01
- Volume
- 94
- Issue
- 4
- Pages
- 633-642
- ISSN
- 0741-5400 (ISSN-L)
- 1938-3673
- OpenAlex
- W2149185484
- Cited by
- 143
- References
- 99
- Citations by year
- 2026: 6 · 2025: 5 · 2024: 8 · 2023: 12 · 2022: 9 · 2021: 18 · 2020: 13 · 2019: 13 · 2018: 7 · 2017: 8 · 2016: 12 · 2015: 17 · 2014: 13 · 2013: 2
- FWCI
- 1.68
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Leukocyte Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- MRC Senior Clinical Fellowship (G0701932)
- MRC (G0700091)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Zebrafish Biomedical Research Applications
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- zebrafish, neutrophils, neutrophil biology, innate immunity, inflammation, transgenic zebrafish, neutrophil recruitment, reverse migration, inflammation resolution, tissue damage, genetic engineering
- MeSH terms
- Animals, Disease Models, Animal, Humans, Immunity, Neutrophils, Zebrafish, Models, Animal, Animals, Genetically Modified
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