- Poster presentation
- Open access
- Published:
CD24-mediated neutrophil death in inflammation: ex vivo study suggesting a potential role in sepsis
Critical Care volume 16, Article number: P81 (2012)
Background
Delayed neutrophil apoptosis is often detected in inflammatory pathologies, including sepsis [1]. CD24 is a small heavily glycosylated cell-surface protein, linked to the membrane by a glycosyl-phosphatidylinositol (GPI) anchor in a wide variety of cells [2]. Cross-ligation of CD24 triggers apoptosis in a human B-cell subset during the early activation stage [3]. Since CD24 is also expressed on neutrophils, we aimed to study its expression in sepsis and its putative role in apoptosis.
Methods
Blood samples were either collected from healthy donors or from sepsis patients at the onset of sepsis and the two following days and surface CD24 expression on neutrophils was analyzed by flow cytometry. Peripheral blood neutrophils were purified from sepsis patients and healthy individuals by positive selection. Whole blood or neutrophils were challenged with lipopoplysaccharide (LPS), TNF, granulocyte-macrophage colony-stimulating factor (GM-CSF), heat-killed Staphylococcus aureus or heat-killed Escherichia coli and CD24 expression assessed by flow cytometry. Neutrophils were cross-linked with anti-human CD24 and assessed for apoptosis after 24 hours of culture. In some experiments, neutrophils were preincubated with caspase inhibitor (z-VAD-fmk) before crosslinking.
Results
Surface expression of CD24 assessed by flow cytometry was significantly altered in neutrophils from sepsis patients compared with healthy controls. Activation of neutrophils with LPS or heat-killed bacteria in whole blood triggers a strong upregulation of CD24 at surface level despite no enhanced expression being observed when the activation was carried out in purified neutrophils. In contrast, TNF and GM-CSG upregulated CD24 in whole blood and in purified neutrophils. CD24 cross-ligation induces caspase-independent apoptosis in human neutrophils. Ex vivo death responses after CD24 ligation in neutrophils from sepsis patients are currently under study.
Conclusion
This is the first report studying the role of CD24 in sepsis patients, linking homeostasis and apoptosis.
References
Bratton DL, Henson PM: Neutrophil clearance: when the party is over, clean-up begins. Trends Immunol 2011, 32: 350-357. 10.1016/j.it.2011.04.009
Fang X, Zheng P, Tang J, Liu Y: CD24: from A to Z. Cell Mol Immunol 2010, 7: 100-103. 10.1038/cmi.2009.119
Suzuki T, Kiyokawa N, Taguchi T, Sekino T, Katagiri YU, Fujimoto J: CD24 induces apoptosis in human B cells via the glycolipid-enriched membrane domains/rafts-mediated signaling system. J Immunol 2001, 166: 5567-5577.
Author information
Authors and Affiliations
Rights and permissions
This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Parlato, M., Souza-Fonseca-Guimaraes, F., Philippart, F. et al. CD24-mediated neutrophil death in inflammation: ex vivo study suggesting a potential role in sepsis. Crit Care 16 (Suppl 3), P81 (2012). https://doi.org/10.1186/cc11768
Published:
DOI: https://doi.org/10.1186/cc11768