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MUCOSAL BIOLOGY
modulation of H,K-ATPase
-subunit gene transcription in Helicobacter pylori infectionDepartment of Medicine, Medical University of South Carolina, Charleston, South Carolina
Submitted 26 July 2006 ; accepted in final form 1 January 2007
Helicobacter pylori infection of the human gastric body induces hypochlorhydria by perturbing acid secretion. H. pylori inhibits parietal cell H,K-ATPase
-subunit (HK
) gene and protein expression, providing a mechanistic basis for clinical hypochlorhydria. Given that H. pylori infection increases gastric mucosal IL-1
, an acid secretory inhibitor, we investigated the role of IL-1
in H. pylori-mediated inhibition of HK
transcription. Human gastric adenocarcinoma (AGS) cells were transfected with promoter-reporter constructs containing human HK
5'-flanking sequence deletions. IL-1
(10 ng/ml) had no effect on the transcriptional activity of six progressively shorter deletion constructs of the HK
promoter (HK
2179HK
340) and significantly stimulated the activity of HK
206, HK
177, HK
165, and HK
102 deletion constructs (80%, 100%, 46%, and 35%, respectively). H. pylori inhibited the transcriptional activity of HK
2179, HK
206, HK
177, and HK
165; IL-1
relieved the H. pylori inhibition of HK
2179 and HK
206 activity but not HK
177 and HK
165 activity. AGS cell pretreatment with a MEK1/2 inhibitor prevented the IL-1
-mediated stimulation, but p38 and JNK pathway inhibitors did not. IL-1
mRNA levels in AGS cells were low and unaffected by H. pylori, and ELISAs of H. pylori-conditioned AGS culture media showed no measurable IL-1
secretion. These data indicate that an IL-1
-dependent cis-response element lies downstream of 206 nt in the HK
promoter and that IL-1
-mediated upregulation of HK
transcription is affected by an ERK1/2 kinase signal pathway. We conclude that an IL-1
-responsive HK
cis element positively regulates HK
gene transcription in shortened deletion constructs and that H. pylori-induced inhibition of HK
transcription is not mediated by IL-1
.
interleukin-1
; gastric acid secretion
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