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Cited by 473

The DOI matches its Crossref record; 60 of the 60 references it cites were found in a registry or an index.

Mechanisms of Degranulation in Neutrophils

Open access
Lacy, Paige·2006·Allergy, Asthma & Clinical Immunology

Abstract

Neutrophils are critical inflammatory cells that cause tissue damage in a range of diseases and disorders. Being bone marrow-derived white blood cells, they migrate from the bloodstream to sites of tissue inflammation in response to chemotactic signals and induce inflammation by undergoing receptor-mediated respiratory burst and degranulation. Degranulation from neutrophils has been implicated as a major causative factor in pulmonary disorders, including severe asphyxic episodes of asthma. However, the mechanisms that control neutrophil degranulation are not well understood. Recent observations indicate that granule release from neutrophils depends on activation of intracellular signalling pathways, including β-arrestins, the Rho guanosine triphosphatase Rac2, soluble NSF attachment protein (SNAP) receptors, the src family of tyrosine kinases, and the tyrosine phosphatase MEG2. Some of these observations suggest that degranulation from neutrophils is selective and depends on nonredundant signalling pathways. This review focuses on new findings from the literature on the mechanisms that control the release of granule-derived mediators from neutrophils.

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Metadata

Authors
Lacy, P.
Venue
Allergy, Asthma & Clinical Immunology
Published
2006-09
Volume
2
Issue
3
Pages
98-108
ISSN
  • 1710-1484 (ISSN-L)
  • 1710-1492
OpenAlex
W1999517476
Cited by
473
References
60
FWCI
0.00
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Mechanisms of Degranulation in Neutrophils. https://app.cochat.ai/papers/10.1186/1710-1492-2-3-98
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Lacy, P. (2006). Mechanisms of Degranulation in Neutrophils. Allergy, Asthma & Clinical Immunology. https://doi.org/10.1186/1710-1492-2-3-98

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.