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Am J Physiol Gastrointest Liver Physiol 292: G1055-G1061, 2007. First published January 4, 2007; doi:10.1152/ajpgi.00338.2006
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MUCOSAL BIOLOGY

IL-1beta modulation of H,K-ATPase {alpha}-subunit gene transcription in Helicobacter pylori infection

Arindam Saha, Charles E. Hammond, Monika Gooz, and Adam J. Smolka

Department 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 {alpha}-subunit (HK{alpha}) gene and protein expression, providing a mechanistic basis for clinical hypochlorhydria. Given that H. pylori infection increases gastric mucosal IL-1beta, an acid secretory inhibitor, we investigated the role of IL-1beta in H. pylori-mediated inhibition of HK{alpha} transcription. Human gastric adenocarcinoma (AGS) cells were transfected with promoter-reporter constructs containing human HK{alpha} 5'-flanking sequence deletions. IL-1beta (10 ng/ml) had no effect on the transcriptional activity of six progressively shorter deletion constructs of the HK{alpha} promoter (HK{alpha}2179–HK{alpha}340) and significantly stimulated the activity of HK{alpha}206, HK{alpha}177, HK{alpha}165, and HK{alpha}102 deletion constructs (80%, 100%, 46%, and 35%, respectively). H. pylori inhibited the transcriptional activity of HK{alpha}2179, HK{alpha}206, HK{alpha}177, and HK{alpha}165; IL-1beta relieved the H. pylori inhibition of HK{alpha}2179 and HK{alpha}206 activity but not HK{alpha}177 and HK{alpha}165 activity. AGS cell pretreatment with a MEK1/2 inhibitor prevented the IL-1beta-mediated stimulation, but p38 and JNK pathway inhibitors did not. IL-1beta 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-1beta secretion. These data indicate that an IL-1beta-dependent cis-response element lies downstream of –206 nt in the HK{alpha} promoter and that IL-1beta-mediated upregulation of HK{alpha} transcription is affected by an ERK1/2 kinase signal pathway. We conclude that an IL-1beta-responsive HK{alpha} cis element positively regulates HK{alpha} gene transcription in shortened deletion constructs and that H. pylori-induced inhibition of HK{alpha} transcription is not mediated by IL-1beta.

interleukin-1beta; gastric acid secretion



Address for reprint requests and other correspondence: A. J. Smolka, Medicine/Gastro CSB 921 E, Medical Univ. of South Carolina, 96 Jonathan Lucas St., Charleston, SC 29425 (e-mail: smolkaaj{at}musc.edu)




This article has been cited by other articles:


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Am. J. Physiol. Gastrointest. Liver Physiol.Home page
A. Saha, C. E. Hammond, M. Gooz, and A. J. Smolka
The role of Sp1 in IL-1{beta} and H. pylori-mediated regulation of H,K-ATPase gene transcription
Am J Physiol Gastrointest Liver Physiol, November 1, 2008; 295(5): G977 - G986.
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Am. J. Physiol. Gastrointest. Liver Physiol.Home page
A. Saha, C. E. Hammond, M. Trojanowska, and A. J. Smolka
Helicobacter pylori-induced H,K-ATPase {alpha}-subunit gene repression is mediated by NF-{kappa}B p50 homodimer promoter binding
Am J Physiol Gastrointest Liver Physiol, March 1, 2008; 294(3): G795 - G807.
[Abstract] [Full Text] [PDF]




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