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The DOI matches its Crossref record; 48 of the 48 references it cites were found in a registry or an index.

Role of Galectin-3 as an Adhesion Molecule for Neutrophil Extravasation During Streptococcal Pneumonia

Sato, Sachiko, Ouellet, Nathalie, Pelletier, Isabelle, Simard, Marie, Rancourt, Ann, Bergeron, Michel G·2002·The Journal of Immunology

Abstract

Recruitment of neutrophils from blood vessels to sites of infection represents one of the most important elements of innate immunity. Movement of neutrophils across blood vessel walls to the site of infection first requires that the migrating cells firmly attach to the endothelial wall. Generally, neutrophil extravasation is mediated at least in part by two classes of adhesion molecules, β2 integrins and selectins. However, in the case of streptococcal pneumonia, recent studies have revealed that a significant proportion of neutrophil diapedesis is not mediated by the β2 integrin/selectin paradigm. Galectin-3 is a β-galactoside-binding lectin implicated in inflammatory responses as well as in cell adhesion. Using an in vivo streptococcal pneumonia mouse model, we found that accumulation of galectin-3 in the alveolar space of streptococcus-infected lungs correlates closely with the onset of neutrophil extravasation. Furthermore, immunohistological analysis of infected lung tissue revealed the presence of galectin-3 in the lung tissue areas composed of epithelial and endothelial cell layers as well as of interstitial spaces. In vitro, galectin-3 was able to promote neutrophil adhesion to endothelial cells. Promotion of neutrophil adhesion by galectin-3 appeared to result from direct cross-linking of neutrophils to the endothelium and was dependent on galectin-3 oligomerization. Together, these results suggest that galectin-3 acts as an adhesion molecule that can mediate neutrophil adhesion to endothelial cells. However, accumulation of galectin-3 in lung was not observed during neutrophil emigration into alveoli induced by Escherichia coli infection, where the majority of neutrophil emigration is known to be β2 integrin dependent. Thus, based on our results, we propose that galectin-3 plays a role in β2 integrin-independent neutrophil extravasation, which occurs during alveolar infection with Streptococcus pneumoniae.

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Metadata

Authors
Sato, S., Ouellet, N., Pelletier, I., Simard, M., Rancourt, A., & Bergeron, M. G.
Venue
The Journal of Immunology
Published
2002-02
Volume
168
Issue
4
Pages
1813-1822
ISSN
  • 0022-1767 (ISSN-L)
  • 1550-6606
OpenAlex
W1593858768
Cited by
253
References
48
FWCI
3.08
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Role of Galectin-3 as an Adhesion Molecule for Neutrophil Extravasation During Streptococcal Pneumonia. https://app.cochat.ai/papers/10.4049/jimmunol.168.4.1813
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Sato, S., Ouellet, N., Pelletier, I., Simard, M., Rancourt, A., & Bergeron, M. G. (2002). Role of Galectin-3 as an Adhesion Molecule for Neutrophil Extravasation During Streptococcal Pneumonia. The Journal of Immunology. https://doi.org/10.4049/jimmunol.168.4.1813

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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.