4.7 Article

Altered Expression of Antimicrobial Peptides in the Upper Gastrointestinal Tract of Patients with Diabetes Mellitus

Journal

NUTRIENTS
Volume 15, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/nu15030754

Keywords

AMP; cathelicidin; defensin; insulin resistance; LL-37

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In this study, the expression of antimicrobial peptides (AMP) in the upper gastrointestinal tract was investigated in different metabolic states. The results showed that there were differences in AMP expression between normal and pathological metabolic states. Additionally, a correlation between vitamin D levels and AMP expression was observed. The findings suggest that reduced AMP expression in the upper gastrointestinal tract may contribute to epithelial barrier dysfunction and increased bacterial translocation in patients with type 2 diabetes.
Antimicrobial peptides (AMP) are essential components of innate immunity with a broad range of antimicrobial activities against bacteria, viruses, and fungi. The aim of this study was to investigate AMP expression in the upper gastrointestinal tract in normal and pathological metabolic states in humans. Furthermore, we examined the correlation between vitamin D levels and AMP expression in the same cohort. Serum concentrations of 25-hydroxyvitamin D3 were measured, and mRNA expression of beta-defensins HBD-1, -2, -3, -4, alpha-defensins HD-5 and -6 and cathelicidin in the upper gastrointestinal tract epithelia were determined by quantitative RT-PCR in 31 individuals (10 with type 2 diabetes, 10 with insulin resistance, and 11 healthy controls). The majority of the cohort showed low vitamin D concentrations, which were negatively correlated with mRNA expression levels of HBD-3 in corpus mucosa. HBD-1 and HBD-3 mRNA were expressed in corpus mucosa, with the former significantly decreased in patients with diabetes. Hence, we conclude that type 2 diabetes is associated with reduced AMP expression in the upper gastrointestinal tract, which might contribute towards epithelial barrier dysfunction and increased bacterial translocation in these patients.

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