Asian-Australasian Journal of Animal Sciences
- Volume 10 Issue 2
- /
- Pages.233-239
- /
- 1997
- /
- 1011-2367(pISSN)
- /
- 1976-5517(eISSN)
DOI QR Code
Hormonal Regulation of Insulin-Like Growth Factor Binding Protein Secretion by a Bovine Mammary Epithelial Cell Line
- Kim, W.Y. (Department of Animal Science, University of California) ;
- Chow, J.C. (Joslin Diabetes Center and Harvard Medical Center) ;
- Hanigan, M.D. (Purina Mills, Inc.) ;
- Calvert, C.C. (Department of Animal Science, University of California) ;
- Ha, J.K. (Department of Animal Science and Technology, College of Agriculture and Life Sciences, Seoul National University) ;
- Baldwin, R.L. (Department of Animal Science, University of California)
- Received : 1996.12.21
- Accepted : 1997.02.21
- Published : 1997.04.01
Abstract
A mammary epithelial cell line (MAC-T) established as a model for lactation was utilized to identify and characterize effects of various hormones upon insulin-like growth factor binding protein secretion. Ligand and immunoblot analyses of conditioned media indicated that insulin-like growth factor binding protein-2 was secreted by MAC-T cells. Insulin-like growth factor-I stimulated insulin-like growth factor binding protein-2 secretion in a dose-dependent manner, but prolactin and bovine somatotropin did not alter insulin-like growth factor binding protein-2 secretion. Insulin increased and cortisol decreased insulin-like growth factor binding protein-2 secretion. Effects of insulin-like growth factor-I on insulin-like growth factor binding protein-2 secretion support previous studies using primary cultures of bovine mammary cells and bovine fibroblasts. Effects of cortisol and insulin on insulin-like growth factor binding protein-2 secretion may be explained by changes in protein synthesis. In addition, supraphysiological doses of insulin can cross-react with the insulin-like growth factor-I receptor and stimulate insulin-like growth factor binding protein-2 secretion. MAC-T cells provide a model system to study mechanisms that regulate local insulin-like growth factor-I bioactivity.