Platelets contain interleukin-1 alpha and beta which are detectable on the cell surface after activation
P Sedlmayr1, A Blaschitz, M Wilders-Truschnig
1Department of Internal Medicine, Karl-Franzens-University, Graz, Austria.
Insights
Interleukin-1 (IL-1) alpha and beta are found in platelet cytoplasm. Following activation, IL-1 is present on the surface, but mainly released upon platelet disintegration.
Area of Science:
- Hematology
- Immunology
- Cell Biology
Background:
- Activated platelets display Interleukin-1 (IL-1) bioactivity.
- The precise localization of IL-1 within platelets remains unclear.
Purpose of the Study:
- To investigate the intracellular and cell surface localization of IL-1 alpha and IL-1 beta in resting and activated platelets.
Main Methods:
- Immunocytological techniques
- Flow cytometry
- Immunogold-silver staining
- Pre-embedding antibody treatment
Main Results:
- IL-1 alpha and IL-1 beta were detected in the cytoplasm of both resting and activated platelets.
- Low-density IL-1 was found on the surface of intact activated platelets, with higher enrichment in damaged platelets.
- Evidence suggests IL-1 adsorption to fibrin fibers and weak binding to activated platelet surfaces.
Conclusions:
- Both IL-1 alpha and IL-1 beta are present in resting and activated platelets.
- IL-1 appears to transfer to the activated platelet surface, but significant release likely occurs only after platelet disintegration.
- Specific subcellular localization of IL-1 within platelets could not be demonstrated.
Abstract:
Activated platelets have been shown previously to exhibit membrane-bound IL-1 bioactivity, which leads to the question of localization of the cytokine in platelets. Using immunocytological and flow cytometric techniques, we found IL-1 alpha and IL-1 beta in the cytoplasma of both resting and thrombin-activated platelets. Immunogold-silver staining of the cell surface of activated platelets as well as preembedding antibody treatment of platelets revealed the presence of IL-1 (alpha and beta) in low density on the surface of intact cells in contrast to distinct enrichment in the cytoplasma of damaged platelets. Fibrin fibres present between cells indicated adsorbance of IL-1. There was also weak binding of anti-IL-1 alpha to the surface of thrombin-activated platelets as shown by flow cytometry. Following activation there appears to be some transfer of IL-1 onto the cell surface of activated cells, the bulk of the cytokine, however, is probably not released prior to platelet disintegration. In summary, we present evidence for the presence of both IL-1 alpha and IL-1 beta in resting and activated platelets without being able to demonstrate localization of the cytokines to specific subcellular structures.
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