The chemiluminescence of peripheral blood monocytes and alveolar macrophages was determined in the presence of luminol and lucigenin, either before or after the cell adherence to the luminometer curvettes. In the case of monocytes, cell adherence induces an increase of luminol-dependent chemilumines
Effect of a marine toxin on human peripheral blood monocytes
β Scribed by Y. Hokama; P. J. Scheuer; T. Yasumoto
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 484 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0887-8013
No coin nor oath required. For personal study only.
β¦ Synopsis
The effect of okadaic acid (OA), a non-TPA (1 2-0-tetradecanoylphorbol-13-acetate)-type tumor promoter, on interleukin 1 (IL-1) synthesis in human peripheral blood monocytes in vitro was examined using immunofluorescence and the mouse thymocyte assays. Stimulation of IL-1 was shown with 0.05 pg ONml (the peak response), while concentrations of greater than 1 .O pg ONml showed significant inhibition of IL-1 synthesis by monocytes in the immunofluorescence analysis. Okadaic acid added directly to mouse thymocytes showed a peak response in IL-1 synthesis at 0.01 pg ONml, while significant inhibition was shown for concentrations of OA greater than 0.1 pg ONml. Supernatants of monocytes exposed to OA gave maximum stimulation at 0.05 pg ONml for both 24 and 48 hr exposures. Significant inhibition of IL-1 synthesis in monocytes was shown by supernatants obtained from monocytes exposed 24 hr with 1 .O pg ONml. Addition of various concentrations of OA to monocyte cultures in the presence of increasing concentrations of monoclonal antibody to OA showed significant reduction of the inhibition of IL-1 synthesis by OA at the 0.10 pg level, but more significantly at the 1 .O pg ONml level. The higher levels of OA associated with inhibition of IL-1 synthesis in monocytes in this study were comparable to the concentrations used in the tumor promotion studies by others. The reversal of the inhibitory effect of OA by the monoclonal antibody to OA is of interest and should be applicable to further studies on the mechanism of OA tumor promotion.
π SIMILAR VOLUMES
The author wishes to acknowledge the excellent technical assistance of Mrs. Melinda Donnelly and Mrs. Ruthann Mullen and to thank F'rofessor William A. Tisdale for support and encouragement.
## ~~~~ ~ ~ ~ Cytogenetic analyses were performed on human peripheral blood lymphocytes exposed to 2450 MHz microwaves during 30 and 120 min at a constant temperature of 36.1 "C (body temperature). The temperature was kept constant by means of a temperature probe put in the blood sample which give