Abstract
Gastrin gene expression is regulated by developmental cues, pH, and inflammation. These processes are mediated by various extracellular ligands, e.g., growth factors, cytokines, and neuropeptides that also stimulate c-fos gene expression. Therefore, to determine whether Fos is required for stimulation of the gastrin promoter, a c-fos sense expression vector was coexpressed with a gastrin reporter construct in a GH4 rat pituitary cell line. We found that epidermal growth factor (EGF) and tumor necrosis factor- α (TNF-α) transiently stimulate an increase in Fos protein that precedes stimulation of the gastrin promoter. However, the induction mediated by TNF- α was weaker than that mediated by EGF, indicating minimal overlap of the signaling pathways activated by EGF and TNF-α. Accordingly, overexpression of c-fos mRNA facilitated primarily EGF rather than TNF-α induction of the gastrin promoter. Expression of the c-fos gene in the absence of ligand did not stimulate the gastrin promoter. Thus c-fos gene expression is required but is not sufficient for induction of the gastrin promoter by EGF.
Original language | English (US) |
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Pages (from-to) | G942-G948 |
Journal | American Journal of Physiology - Gastrointestinal and Liver Physiology |
Volume | 271 |
Issue number | 6 34-6 |
DOIs | |
State | Published - 1996 |
Externally published | Yes |
Keywords
- AP-1
- cytokines
- deoxyribonucleic acid element
- gastrin epidermal growth factor response element
- tumor necrosis factor-α
ASJC Scopus subject areas
- Physiology
- Hepatology
- Gastroenterology
- Physiology (medical)