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Updated: Apr 17, 2026

Measuring Local Anaphylaxis in Mice
Published on: October 14, 2014
Responsible cell type in murine PAF-induced systemic anaphylaxis
Tomoyuki Suzuki1, Keisuke Yanagida2, Takao Shimizu3
1Department of Lipid Life Science, National Institute of Global Health and Medicine, Japan Institute for Health Security, Tokyo, Japan.
Abstract:
Platelet-activating factor (PAF) is a key mediator of systemic anaphylaxis. The principal target cell type of PAF in systemic anaphylaxis remains unclear. Endothelial cell-specific PAFR-deficient mice were protected from mortality in PAF-induced systemic anaphylaxis. Endothelial PAFR is suggested to be the principal target mediating PAF-driven mortality in systemic anaphylaxis.
Insights
Platelet-activating factor (PAF) is crucial in anaphylaxis. Targeting endothelial PAF receptors (PAFR) protects against PAF-induced mortality, suggesting endothelial cells are the main mediators.
Area of Science:
- Immunology
- Cell Biology
- Pharmacology
Background:
- Platelet-activating factor (PAF) is a critical mediator in systemic anaphylaxis.
- The specific cell type targeted by PAF during anaphylaxis is not well understood.
Purpose of the Study:
- To determine the principal cell type targeted by PAF in systemic anaphylaxis.
- To investigate the role of endothelial PAF receptors (PAFR) in PAF-mediated anaphylaxis.
Main Methods:
- Utilized endothelial cell-specific PAFR-deficient mice.
- Administered PAF to induce systemic anaphylaxis.
- Monitored mortality rates in genetically modified and control mice.
Main Results:
- Endothelial cell-specific PAFR-deficient mice showed significant protection from mortality.
- This protection indicates that endothelial PAFR plays a crucial role in PAF-induced anaphylaxis.
Conclusions:
- Endothelial PAFR is identified as the principal target mediating PAF-driven mortality in systemic anaphylaxis.
- Targeting endothelial PAFR represents a potential therapeutic strategy for managing anaphylaxis.
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