Monensin and forskolin inhibit the transcription rate of sucrase-isomaltase but not the stability of its mRNA in Caco-2 cells
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(93)80964-V/fullpdf
Reference22 articles.
1. Perturbation of vesicular traffic with the carboxylic ionophore monensin
2. Enterocytic differentiation and glucose utilization in the human colon tumor cell line Caco-2: Modulation by forskolin
3. Inhibition of the post-translational processing of microvillar hydrolases is associated with a specific decreased expression of sucrase-isomaltase and an increased turnover of glucose in Caco-2 cells treated with monensin
4. Reversible forskolin-induced impairment of sucrase-isomaltase mRNA levels, biosynthesis, and transport to the brush border membrane in Caco-2 cells
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1. Synthesis and biological evaluation of chemical tools for the study of Dolichol Linked Oligosaccharide Diphosphatase (DLODP);European Journal of Medicinal Chemistry;2017-01
2. Impairments in enzyme activity and biosynthesis of brush border-associated hydrolases in human intestinal Caco-2/TC7 cells infected by members of the Afa/Dr family of diffusely adhering Escherichia coli;Cellular Microbiology;2001-05
3. Immunological Analysis of β-Thalassemic Mouse Intestinal Proteins Reveals Up-Regulation of Sucrase-Isomaltase in Response to Iron Overload;The Journal of Nutrition;1999-05-01
4. Two HNF-1 binding sites govern the glucose repression of the human sucrase-isomaltase promoter;Biochemical Journal;1998-11-15
5. Selecting agent hygromycin B alters expression of glucose-regulated genes in transfected Caco-2 cells;American Journal of Physiology-Gastrointestinal and Liver Physiology;1998-05-01
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