Cellular differentiation of non-transformed intestinal epithelial cells is regulated by Lactobacillus rhamnosus and L. casei strains
Language English Country Czech Republic Media print-electronic
Document type Journal Article
PubMed
29303613
DOI
10.33549/physiolres.933643
PII: 933643
Knihovny.cz E-resources
- MeSH
- beta Catenin biosynthesis MeSH
- Cell Differentiation drug effects MeSH
- Cytokines biosynthesis MeSH
- Epithelial Cells drug effects MeSH
- Interleukin-18 biosynthesis MeSH
- Caspase 1 biosynthesis MeSH
- Rats MeSH
- Lacticaseibacillus rhamnosus * MeSH
- Lacticaseibacillus casei * MeSH
- RNA, Messenger biosynthesis MeSH
- Microfilament Proteins biosynthesis MeSH
- Probiotics pharmacology MeSH
- Gene Expression Regulation drug effects MeSH
- Intestinal Mucosa cytology drug effects MeSH
- Subcellular Fractions metabolism MeSH
- Toll-Like Receptors biosynthesis drug effects MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- beta Catenin MeSH
- Ctnnb1 protein, rat MeSH Browser
- Cytokines MeSH
- Interleukin-18 MeSH
- Caspase 1 MeSH
- RNA, Messenger MeSH
- Microfilament Proteins MeSH
- Toll-Like Receptors MeSH
- Vil1 protein, rat MeSH Browser
The aim of this study was to characterize an in vitro modulating effect of three commensal Lactobacillus strains on cellular differentiation of non-transformed crypt-like rat small intestinal cell line IEC-18. IEC-18 was grown on extracellular matrix, with or without presence of Lactobacillus strains. Gene expression of IEC-18 bacterial detection system - such as Toll-like receptors TLR-2, TLR-4, signal adapter MyD88, cytoplasmic NOD2 receptor, inflammatory cytokines IL-18, IL-1beta, chemokine IL-8 and enzyme caspase-1 - was evaluated using real-time PCR. Expression and localization of TLR-2, TLR-4, IL-18 and caspase-1 proteins was demonstrated by Western blotting and immunofluorescent staining. Secretion of IL-18 to apical and basolateral surfaces was assayed by ELISA. Our results suggested that L. casei LOCK0919 accelerated differentiation of IEC-18 by stimulating TLR-2, TLR-4, MyD88, IL-18, caspase-1 mRNAs and proteins. L. casei LOCK0919 increased expression and transfer of villin and beta-catenin from cytoplasm to cell membrane. Presence of L. rhamnosus LOCK0900 resulted in detachment of IEC-18 layer from extracellular matrix leading to induction of IL-1beta, of TLR-2 and IL-8 mRNAs and stimulation of MyD88, caspase-1 and cytosolic receptor NOD2 mRNAs. L. rhamnosus LOCK0908 was not recognized by TLR-2 or TLR-4 receptors. Lactobacilli-IEC-18 crosstalk enhanced immune and barrier mucosal functions.
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