Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Frederick M. Stanley"'
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0138097 (2015)
Plasminogen activator inhibitor type 1 (PAI-1) is a multifunctional protein that has important roles in inflammation and wound healing. Its aberrant regulation may contribute to many disease processes such as heart disease. The PAI-1 promoter is resp
Externí odkaz:
https://doaj.org/article/90648e96498f45e38ca5e1ab54016c9e
Autor:
Frederick M. Stanley, Anthony I. Vulin
Publikováno v:
Journal of Biological Chemistry. 279:25172-25178
Oxidative stress is one of the characteristics of diabetes and is thought to be responsible for many of the pathophysiological changes caused by the disease. We previously identified an insulin response element in the promoter of plasminogen activato
Autor:
Frederick M. Stanley, Anthony I. Vulin
Publikováno v:
Journal of Biological Chemistry. 277:20169-20176
Plasminogen activator inhibitor-1 (PAI-1) is an important regulator of fibrinolysis by its inhibition of both tissue-type and urokinase plasminogen activators. PAI-1 levels are elevated in type II diabetes and this elevation correlates with macro- an
Publikováno v:
Molecular and Cellular Endocrinology. 186:7-16
Insulin treatment increased prolactin gene expression in GH4 cells, a rat pituitary tumor cell line, through the endogenous insulin receptor. However, insulin regulation of transfected plasmids required the expression of cotransfected insulin recepto
Autor:
Kirsten K. Jacob, Frederick M. Stanley
Publikováno v:
Endocrinology. 140:4542-4550
The sequence −101/−92 of the PRL promoter has been shown to be essential for both basal and hormone-increased PRL gene transcription. It is important to identify transcription factors that bind to this sequence if we are to understand the regulat
Publikováno v:
Molecular and Cellular Endocrinology. 152:137-145
Epidermal growth factor (EGF) increases prolactin gene expression in GH4 cells, but the promoter element(s) required for this response has not been clearly defined. We identified a bipartite element −96/−87, −76/−67 in the rat proximal promot
Publikováno v:
Journal of Biological Chemistry. 273:4800-4809
A physiologically relevant response to insulin, stimulation of prolactin promoter activity in GH4 pituitary cells, was used as an assay to study the specificity of protein-tyrosine phosphatase function. Receptor-like protein-tyrosine phosphatase alph
Publikováno v:
Molecular and cellular endocrinology. 382(1)
Insulin increases prolactin gene expression in GH4 cells through phosphorylation of Elk-1 (Jacob and Stanley, 2001). We preformed a reverse two-hybrid screen using Elk-1-B42 as bait to identify proteins from GH4 cells that might serve as co-activator
Publikováno v:
Journal of Biological Chemistry. 271:10425-10428
The insulin-response element from the prolactin gene is identical to the Ets-binding site, and dominant-negative Ets protein inhibits insulin-increased prolactin gene expression. Immunoblotting identified the Ets-related transcription factor GABP in
Autor:
Frederick M. Stanley, Kirsten K. Jacob
Publikováno v:
Molecular and Cellular Endocrinology. 109:175-181
Insulin and cAMP stimulate prolactin gene transcription and prolactin-CAT expression in rat pituitary tumor GH cells. Expression of prolactin-CAT construct, pPrl(−173/+75)CAT, is stimulated 10- to 30-fold by either insulin or cAMP Addition of both