Incubation of Swiss mouse 3T3 cells at 37Β°C with bovine brain-derived growth factor (BDGF) decreased the cell surface '251-EGF binding activity of these cells by 70-80%. This down-modulation of the EGF receptor by BDGF was time, temperature, and dose dependent. Scatchard plot analysis indicated that
Effect of serum and growth factors on heat sensitivity in Swiss mouse 3T3 cells
β Scribed by Dr. Roeland van Wijk; Angela M. Otto; Luis Jimenez De Asua
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 940 KB
- Volume
- 119
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Quiescent Swiss mouse 3T3 cells react to a heat treatment at 46Β°C for 20 min by changing their flat, wellβextended morphology to a round appearance with retracted cytoplasmic processes during the subsequent 2 h at 37Β°C. The percentage of morphologically changed cells was used to quantify changes in heat sensitivity, or resistance, in response to mitogenic stimulation. Stimulating quiescent cells with serum or with the specific growth factors epidermal growth factor (EGF) and prostaglandin F~2Ξ±~ (PGF~2Ξ±~) markedly increased the heat resistance to a 46Β°C treatment, but only when the heat treatment, but only when the heat treatment was applied within 2β3 h after the addition. When insulin (which is not mitogenic, but synergistic with EGF and PGF~2Ξ±~ in these cells) was added alone or in combination with either EGF or PGF~2Ξ±~, it had no effect on the development of heat resistance. Neither did cycloheximide nor tunicamycin inhibit heat resistance induced by EGF, and cycloheximide even enhanced it after 2β4 h. However, adding colcemid before or at the beginning of the heat treatment abolished the increased heat resistance. The results indicate that the resistance to a single heat treatment at 46Β°C may be related to changes in the metabolic state after mitogenic stimulation, even though these changes need not be reflected in the rate of entry into S phase. Furthermore, the cytoskeletal organization appears to be a crucial component in heat resistance of Swiss 3T3 cells.
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