A number of single-cell-cloned cell lines have been used to examine the growth-promoting effects of putative mammotrophic agents on the various cell types in normal and neoplastic rat mammary glands. A partially purified novel pituitary-derived growth factor stimulates only cuboidal epithelial cells
Appearance of basic fibroblast growth factor receptors upon differentiation of rat mammary epithelial to myoepithelial-like cells in culture
✍ Scribed by David G. Fernig; John A. Smith; Philip S. Rudland
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 815 KB
- Volume
- 142
- Category
- Article
- ISSN
- 0021-9541
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✦ Synopsis
Abstract
The binding of [^125^I]‐epidermal growth factor (EGF) and [^125^I]‐basic fibroblast growth factor (bFGF) to a number of single‐cell cloned rat mammary cell lines was measured using a saturation assay. Similar numbers of high‐affinity [^125^I]‐EGF binding sites (K~D~ 1.3 nM) were found in epithelial and myoepithelial‐like cell lines. In contrast, high‐affinity (K~D~ 35–276 pM) [^125^I]‐bFGF binding sites were present on fibroblastic and myoepithelial‐like cell lines but were not detectable on epithelial cell lines. A series of cell lines representing stages in the differentiation pathway of epithelial cells to an elongated myoepithelial‐like morphology showed a graded increase in the number of bFGF receptors. The sensitivity of a cell line to stimulation of DNA synthesis by bFGF correlated with the level of expression of bFGF receptors on the cellular surface. Complexes of cell surface receptors affinity‐cross‐linked to [^125^I]‐bFGF were analysed by sodium dodecyl sulfate‐polyacrylamide gel electrophoresis (SDS‐PAGE). In each case two distinct complexes having apparent molecular weights of 180 kDa and 160 kDa were observed.
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## Abstract We have previously demonstrated that insulin‐like growth factor binding protein‐5 (IGFBP‐5) is upregulated following treatment of the mouse mammary epithelial cell line HC11 with lactogenic hormones (dexamethasone, insulin, and prolactin—DIP). In addition, we have also shown that IGFBP‐