## Abstract In this study the effects of retinoic acid on the binding and mitogenic activity of epidermal growth factor (EGF) in mouse fibroblast Balb/c 3T6 cells are further examined. Retinoic acid treatment of 3T6 cells results in a sixfold enhancement of ^125^Iโlabeled mouse EGF binding when ass
Antagonistic action of retinoic acid and teleocidin on the proliferation and epidermal growth factor binding of rat hepatoma cells
โ Scribed by Yoshiyasu Kaneko
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- French
- Weight
- 563 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0020-7136
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โฆ Synopsis
Abstract
Rat hepatoma cells were cultured in a medium with suboptimal concentration of fetal calf serum. In this low serum culture, retinoic acid inhibited the cell proliferation and enhanced the number of receptors for epidermal growth factor (EGF). On the contrary, teleocidin, a possible naturally occurring tumor promoter from Streptomyces, was a weak mitogen and inhibited EGF binding. A concurrent treatment of AH66 cells with these two compounds showed that they acted antagonistically. Retinoic acid inhibited the mitogenic action of teleocidin, while teleocidin suppressed the retinoicโacid enhancement of the number of EGF receptors. Retinoic acid could not prevent the alterations of the cell surface properties induced by a prolonged treatment with teleocidin. Furthermore, these two compounds appeared to be involved in the regulation of glycoprotein synthesis and the stimulation of cellular glycoprotein synthesis by retinoic acid was abolished by teleocidin. The present data suggest that retinoic acid selectively antagonizes the mitogenic action of teleocidin, and also indicate that the hepatoma cell cultures appear to provide a useful system for exploring the mechanisms of action of both retinoic acid and teleocidin.
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We observed that all-trans-retinoic acid (RA) down-regulated insulin-like growth factor binding proteins (IGFBPs) in cultured human hepatoma cells (Hep 3B, PLC/PRF/5, and Hep G2); therefore, we characterized the role of this down-regulation in cell growth. Treatment with 10 micromol/L RA revealed a
## Abstract The effects of epidermal growth factor (EGF) were studied in rat pituitary tumor cells, GH~3~, grown in serumโsupplemented and serumโfree chemically defined media. EGF (1 nM) increased the cell number to 132% of the control cultured in the defined medium during a 6โday incubation period
## Abstract Binding of ^125^Iโepidermal growth factor (EGF) to purified populations of rat astrocytes, oligodendrocytes, and neurons was measured. Astrocytes bound 40,000โ100,000 EGF molecules per cell, while oligodendrocytes bound only 6,000โ10,000 EGF molecules per cell. In contrast, neurons had
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