Literature DB >> 26817586

Early Molecular Events in Murine Gastric Epithelial Cells Mediated by Helicobacter pylori CagA.

Aditi Banerjee1, Malini Basu2, Thomas G Blanchard3, Subba R Chintalacharuvu4, Wei Guang1, Erik P Lillehoj1, Steven J Czinn1.   

Abstract

BACKGROUND: Murine models of Helicobacter pylori infection are used to study host-pathogen interactions, but lack of severe gastritis in this model has limited its usefulness in studying pathogenesis. We compared the murine gastric epithelial cell line GSM06 to the human gastric epithelial AGS cell line to determine whether similar events occur when cultured with H. pylori.
MATERIALS AND METHODS: The lysates of cells infected with H. pylori isolates or an isogenic cagA-deficient mutant were assessed for translocation and phosphorylation of CagA and for activation of stress pathway kinases by immunoblot.
RESULTS: Phosphorylated CagA was detected in both cell lines within 60 minutes. Phospho-ERK 1/2 was present within several minutes and distinctly present in GSM06 cells at 60 minutes. Similar results were obtained for phospho-JNK, although the 54 kDa phosphoprotein signal was dominant in AGS, whereas the lower molecular weight band was dominant in GSM06 cells.
CONCLUSION: These results demonstrate that early events in H. pylori pathogenesis occur within mouse epithelial cells similar to human cells and therefore support the use of the mouse model for the study of acute CagA-associated host cell responses. These results also indicate that reduced disease in H. pylori-infected mice may be due to lack of the Cag PAI, or by differences in the mouse response downstream of the initial activation events.
© 2016 John Wiley & Sons Ltd.

Entities:  

Keywords:  CagA; Helicobacter pylori; translocation; type 4 secretion system

Mesh:

Substances:

Year:  2016        PMID: 26817586      PMCID: PMC4965344          DOI: 10.1111/hel.12300

Source DB:  PubMed          Journal:  Helicobacter        ISSN: 1083-4389            Impact factor:   5.753


  54 in total

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