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Published on: May 7, 2018
Gastric de novo Muc13 expression and spasmolytic polypeptide-expressing metaplasia during Helicobacter heilmannii
Cheng Liu1, Annemieke Smet2, Caroline Blaecher1
1Department of Pathology, Bacteriology and Avian Diseases, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
Abstract:
Helicobacter heilmannii is a zoonotic bacterium that has been associated with gastric disease in humans. In this study, the mRNA expression of mucins in the stomach of BALB/c mice was analyzed at several time points during a 1-year infection with this bacterium, during which gastric disease progressed in severity. Markers for acid production by parietal cells and mucous metaplasia were also examined. In the first 9 weeks postinfection, the mRNA expression of Muc6 was clearly upregulated in both the antrum and fundus of the stomach of H. heilmannii-infected mice. Interestingly, Muc13 was upregulated already at 1 day postinfection in the fundus of the stomach. Its expression level remained high in the stomach over the course of the infection. This mucin is, however, not expressed in a healthy stomach, and high expression of this mucin has so far only been described in gastric cancer. In the later stages of infection, mRNA expression of H(+)/K(+)-ATPase α/β and KCNQ1 decreased, whereas the expression of Muc4, Tff2, Dmbt1, and polymeric immunoglobulin receptor (pIgR) increased starting at 16 weeks postinfection onwards, suggesting the existence of spasmolytic polypeptide-expressing metaplasia in the fundus of the stomach. Mucous metaplasia present in the mucosa surrounding low-grade mucosa-associated lymphoid tissue (MALT) lymphoma-like lesions was also histologically confirmed. Our findings indicate that H. heilmannii infection causes severe gastric pathologies and alterations in the expression pattern of gastric mucins, such as Muc6 and Muc13, as well as disrupting gastric homeostasis by inducing the loss of parietal cells, resulting in the development of mucous metaplasia.
Insights
Helicobacter heilmannii infection in mice significantly alters stomach mucin expression, leading to gastric disease and metaplasia. Key mucins like Muc6 and Muc13 show early changes, while others indicate metaplasia development.
Area of Science:
- Gastroenterology
- Microbiology
- Molecular Biology
Background:
- Helicobacter heilmannii is a zoonotic bacterium linked to human gastric disease.
- Gastric pathology involves complex changes in cellular function and gene expression.
Purpose of the Study:
- To investigate the impact of H. heilmannii infection on gastric mucin mRNA expression in mice.
- To analyze changes in acid production markers and mucous metaplasia during infection.
Main Methods:
- BALB/c mice were infected with H. heilmannii for up to 1 year.
- mRNA expression of mucins (Muc6, Muc13, Muc4), acid production markers (H+/K+-ATPase), and metaplasia markers (Tff2, Dmbt1, pIgR) were analyzed.
- Histological examination of gastric mucosa was performed.
Main Results:
- Muc6 mRNA was upregulated within 9 weeks, and Muc13 mRNA was upregulated by day 1 in infected mice.
- Later infection stages showed decreased acid production markers and increased Muc4, Tff2, Dmbt1, and pIgR expression.
- Mucous metaplasia was confirmed histologically, particularly around MALT lymphoma-like lesions.
Conclusions:
- H. heilmannii infection induces significant gastric pathologies and alters gastric mucin expression patterns.
- The bacterium disrupts gastric homeostasis, causing parietal cell loss and promoting mucous metaplasia.
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