Numerous studies have shown that prolactin (PRL) production by GH, cells grown in serum supplemented media is regulated by several hormones including thyroliberin (TRH). The recent availability of hormonally d e fined, serum-free media for the growth of GH, cells has made it possible to determine th
The effects of epidermal growth factor on cell proliferation and prolactin production by GH3 rat pituitary cells
✍ Scribed by Yukiko Yajima; Toshikazu Saito
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 918 KB
- Volume
- 120
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The effects of epidermal growth factor (EGF) were studied in rat pituitary tumor cells, GH~3~, grown in serum‐supplemented and serum‐free chemically defined media. EGF (1 nM) increased the cell number to 132% of the control cultured in the defined medium during a 6‐day incubation period, while it decreased the cell number to 60% of the control in the serum‐supplemented medium. EGF altered the morphology of the cells grown in the defined medium more markedly to an elongated conformation than that of cells grown in the serum‐supplemented medium. EGF also stimulated prolactin (PRL) production by culture in the presence or absence of serum. The effects of the cell density of GH~3~ on the action of EGF were shown to appear in two ways. The mitogenic influence of EGF was more effective on, and more responsive to, high‐density cells, whereas the stimulatory action on PRL production was less effective on high‐density cells. However, the inhibitory effects on cellular growth appeared independently of cell densities. The results obtained with ^125^I‐EGF binding experiments indicated that the number of binding sites, affinity, and internalization of EGF receptors were similar in either serum‐supplemented or serum‐free culture. At low cell density, the number of available ^125^I‐EGF binding sites per cell was larger than at high cell density. These results suggested that there was no apparent correlation between EGF binding and its differing effects on the growth of GH~3~ cultured in the serum‐supplemented and the defined medium.
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