Comparison of the Regulation of Carboxypeptidase E and Prolactin in GH4C1 Cells, a Rat Pituitary Cell Line
- 1 January 1990
- journal article
- research article
- Published by S. Karger AG in Neuroendocrinology
- Vol. 51 (6) , 658-663
- https://doi.org/10.1159/000125407
Abstract
The treatment of GH4C1 cells, a prolactin-producing rat anterior pituitary cell line, with estradiol (1 nM), insulin (300 nM) and epidermal growth factor (10 nM) has been previously shown to substantially increase both the intracellular level of prolactin, as well as the number of secretory granules. In this study, we examined the effect of this treatment on levels of carboxypeptidase E (CPE), a prohormone-processing enzyme. GH4C1 cells contain CPE mRNA and enzymatic activity. The secretion of both prolactin and CPE activity from GH4C1 cells is stimulated 10-fold by 50 ml KCl and 2- to 3-fold by 100 nM thyrotropin-releasing hormone, suggesting that these two proteins are contained in secretory granules. Treatment of GH4C1 cells with estradiol, insulin, and epidermal growth factor causes an increase in the intracellular level of CPE to approximately 2-fold of control values. This change is much smaller than the change in the level of prolactin: intracellular prolactin is increased 140-fold by the treatment. Kinetic analysis of the CPE activity indicates that the treatment does not alter the Km of substrate hydrolysis, with the change in activity the result of an increase in apparent Vmax. Northern blot analysis indicates that the level of CPE mRNA is not influenced (1 cell line, although some regulation of CPE activity does occur.Keywords
This publication has 21 references indexed in Scilit:
- Secretion and Regulation of Two Biosynthetic Enzyme Activities, Peptidyl-Glycineα-Amidating Monooxygenase and a Carboxypeptidase, by Mouse Pituitary Corticotropic Tumor Cells*Endocrinology, 1984
- Synergistic stimulation of prolactin release by phorbol ester, A23187 and forskolinBiochemical and Biophysical Research Communications, 1984
- Carboxypeptidase B-like converting enzyme activity in secretory granules of rat pituitary.Proceedings of the National Academy of Sciences, 1984
- Purification and Characterization of a Membrane‐Bound Enkephalin‐Forming Carboxypeptidase, “Enkephalin Convertase”Journal of Neurochemistry, 1984
- Purification and characterization of enkephalin convertase, an enkephalin-synthesizing carboxypeptidase.Journal of Biological Chemistry, 1983
- Enkephalin convertase: purification and characterization of a specific enkephalin-synthesizing carboxypeptidase localized to adrenal chromaffin granules.Proceedings of the National Academy of Sciences, 1982
- Purification of Mouse Immunoglobulin Heavy‐Chain Messenger RNAs from Total Myeloma Tumor RNAEuropean Journal of Biochemistry, 1980
- Efficient transfer of large DNA fragments from agarose gels to diazobenzyloxymethyl-paper and rapid hybridization by using dextran sulfate.Proceedings of the National Academy of Sciences, 1979
- Rapid colorimetric assay of β-galactosidase and N-acetyl-β-glucosaminidase in human urineClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- Establishment of Clonal Strains of Rat Pituitary Tumor Cells That Secrete Growth Hormone1,2Endocrinology, 1968