Fos is required for EGF stimulation of the gastrin promoter

被引:10
作者
Marks, P
Iyer, G
Cui, YQ
Merchant, JL
机构
[1] UNIV MICHIGAN, DEPT INTERNAL MED, ANN ARBOR, MI 48109 USA
[2] UNIV MICHIGAN, DEPT PHYSIOL, ANN ARBOR, MI 48109 USA
[3] HOWARD HUGHES MED INST, ANN ARBOR, MI 48109 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 1996年 / 271卷 / 06期
关键词
AP-1; tumor necrosis factor-alpha; cytokines; gastrin epidermal growth factor response element; deoxyribonucleic acid element;
D O I
10.1152/ajpgi.1996.271.6.G942
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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 GH(4) rat pituitary cell line. We found that epidermal growth factor (EGF) and tumor necrosis factor-alpha (TNF-alpha) transiently stimulate an increase in Fos protein that precedes stimulation of the gastrin promoter. However, the induction mediated by TNF-alpha was weaker than that mediated by EGF, indicating minimal overlap of the signaling pathways activated by EGF and TNF-alpha. Accordingly, overexpression of c-fos mRNA facilitated primarily EGF rather than TNF-alpha 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.
引用
收藏
页码:G942 / G948
页数:7
相关论文
共 33 条
[1]  
ANDERSSON S, 1989, J BIOL CHEM, V264, P8222
[2]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157
[3]   PHORBOL ESTER INDUCIBLE GENES CONTAIN A COMMON CIS ELEMENT RECOGNIZED BY A TPA-MODULATED TRANS-ACTING FACTOR [J].
ANGEL, P ;
IMAGAWA, M ;
CHIU, R ;
STEIN, B ;
IMBRA, RJ ;
RAHMSDORF, HJ ;
JONAT, C ;
HERRLICH, P ;
KARIN, M .
CELL, 1987, 49 (06) :729-739
[4]   THE REGULATION BY GROWTH-HORMONE OF LIPOPROTEIN-LIPASE GENE-EXPRESSION IS MEDIATED BY C-FOS PROTOONCOGENE [J].
BARCELLINICOUGET, S ;
PRADINESFIGUERES, A ;
ROUX, P ;
DANI, C ;
AILHAUD, G .
ENDOCRINOLOGY, 1993, 132 (01) :53-60
[5]   PARASITISM BY THE SLOW BACTERIUM HELICOBACTER-PYLORI LEADS TO ALTERED GASTRIC HOMEOSTASIS AND NEOPLASIA [J].
BLASER, MJ ;
PARSONNET, J .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (01) :4-8
[6]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]   PROLONGED ACTIVATION OF JUN AND COLLAGENASE GENES BY TUMOR NECROSIS FACTOR-ALPHA [J].
BRENNER, DA ;
OHARA, M ;
ANGEL, P ;
CHOJKIER, M ;
KARIN, M .
NATURE, 1989, 337 (6208) :661-663
[8]  
BUNDGAARD JR, 1995, FEBS LETT, V369, P225
[9]   EFFECT OF INCREASING HELICOBACTER-PYLORI AMMONIA PRODUCTION BY UREA INFUSION ON PLASMA GASTRIN-CONCENTRATIONS [J].
CHITTAJALLU, RS ;
NEITHERCUT, WD ;
MACDONALD, AMI ;
MCCOLL, KEL .
GUT, 1991, 32 (01) :21-24
[10]   MUCOSAL TUMOR-NECROSIS-FACTOR-ALPHA AND INTERLEUKIN-6 IN PATIENTS WITH HELICOBACTER-PYLORI ASSOCIATED GASTRITIS [J].
CRABTREE, JE ;
SHALLCROSS, TM ;
HEATLEY, RV ;
WYATT, JI .
GUT, 1991, 32 (12) :1473-1477