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Endocrinology, doi:10.1210/endo-113-3-871
Endocrinology Vol. 113, No. 3 871-877
Copyright © 1983 by the Endocrine Society.
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Epidermal Growth Factor Stimulates Cell Proliferation and Inhibits Functional Differentiation of Mouse Mammary Epithelial Cells in Culture*

YUJI TAKETANI and TAKAMI OKA

Laboratory of Biochemistry and Metabolism, National Institute of Arthritis, Diabetes, and Digestive and Kidney Diseases, National Institutes of Health Bethesda, Maryland 20205

Address requests for reprints to: Dr. Takami Oka, Building 10,Room 9B15, National Institutes of Health, Bethesda, Maryland 20205.

Abstract

Mouse mammary epithelial cells cultured on collagen gels multiplied and produced casein and a-lactalbumin in response to insulin, cortisol, and PRL. The addition of epidermal growth factor (EGF) at 50 ng/ml increased the total number of epithelial cells by 30–40% and thymidine incorporation into DNA 4.7-fold after 5 days of culture. In contrast, EGF inhibited hormonal induction of the synthesis of casein and alactalbumin in those cells by about 45% and 55%, respectively, without inhibiting total protein synthesis. Furthermore, EGF decreased casein mRNA activity by 55% and increased total mRNA activity by 66% in cells cultured with the three hormones. These effects of EGF were apparent at 0.1 ng/ml and were maximal at 50–100 ng/ml and could be reversed by its removal from the medium, followed by the addition of anti-EGF antibody. The inhibition of casein synthesis by EGF was unaffected by the concentrations of insulin, cortisol, and PRL. Other growth factors, such as fibroblast growth factor, multiplication-stimulating activity, nerve growth factor, and platelet-derived growth factor, did not simulate the effects of EGF. Cytarabine (1 µg/ ml), which inhibited thymidine incorporation into DNA by 94%, did not block the inhibitory action of EGF on casein synthesis. These results suggest that EGF serves as a regulator of hormonedependent growth and differentiation of mammary epithelial cells. (Endocrinology 113: 871, 1983)

Footnotes

* A preliminary account of this work was presented at the 73rd Annual Meeting of the American Society of Biological Chemists, New Orleans, LA, April 18–23,1982.

Received December 23, 1982.




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