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RANTES augments radical oxygen products from eosinophils
J Chihara1, N Hayashi, T Kakazu
1Fourth Department of Internal Medicine, Kinki University School of Medicine, Osakasayama, Japan.
International Archives of Allergy and Immunology
|January 1, 1994
Summary
Platelets release RANTES, a cytokine that enhances eosinophil activation and radical oxygen product generation. This suggests platelets contribute to allergic inflammation by promoting eosinophil infiltration and activity.
Area of Science:
- Immunology
- Cell Biology
- Allergic Inflammation Research
Background:
- RANTES (Regulated on Activation, Normal T Cell Expressed and Secreted) is an 8-kD cytokine released by activated platelets.
- RANTES exhibits chemotactic activity, attracting eosinophils to sites of inflammation.
- Eosinophils play a role in allergic inflammatory responses.
Purpose of the Study:
- To investigate the effect of RANTES on radical oxygen product (ROS) generation by eosinophils.
- To elucidate the role of platelet-derived RANTES in eosinophil activation and allergic inflammation.
Main Methods:
- Eosinophil cell lines (EoL-1, EoL-3) and primary human eosinophils were used.
- Cells were stimulated with A23187 ionophore.
- Luminol-dependent chemiluminescence assay was employed to measure ROS production.
- RANTES treatment was administered to assess its impact on ROS generation.
Main Results:
- RANTES treatment significantly enhanced the peak and integrated values of ROS production in EoL-3 cells stimulated with A23187.
- Similar enhancement of ROS production was observed in EoL-1 cells and primary eosinophils upon RANTES treatment.
- These findings indicate RANTES activates eosinophils, leading to increased ROS release.
Conclusions:
- Platelets, through the release of RANTES, play a significant role in allergic inflammation.
- RANTES contributes to allergic pathogenesis by facilitating selective eosinophil infiltration and activation.
- Platelet-derived RANTES is a key mediator in amplifying eosinophil-driven inflammatory responses.