Phosphorylation-dependent immunomodulatory properties of B.PAT polysaccharide isolated from Bifidobacterium animalis ssp. animalis CCDM 218
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
PubMed
39218543
DOI
10.1016/j.carbpol.2024.122518
PII: S0144-8617(24)00744-6
Knihovny.cz E-resources
- Keywords
- Bifidobacterium, Dephosphorylation, Immunomodulation, Polysaccharides, Postbiotics, Surface antigens,
- MeSH
- Polysaccharides, Bacterial pharmacology chemistry isolation & purification MeSH
- Bifidobacterium animalis * chemistry MeSH
- HT29 Cells MeSH
- Caco-2 Cells MeSH
- Cytokines metabolism MeSH
- Dendritic Cells drug effects immunology metabolism MeSH
- Phosphorylation drug effects MeSH
- Immunologic Factors pharmacology chemistry isolation & purification MeSH
- Lacticaseibacillus rhamnosus chemistry MeSH
- Humans MeSH
- Mice MeSH
- Probiotics pharmacology MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Polysaccharides, Bacterial MeSH
- Cytokines MeSH
- Immunologic Factors MeSH
A wide range of articles describe the role of different probiotics in the prevention or treatment of various diseases. However, currently, the focus is shifting from whole microorganisms to their easier-to-define components that can confer similar or stronger benefits on the host. Here, we aimed to describe polysaccharide B.PAT, which is a surface antigen isolated from Bifidobacterium animalis ssp. animalis CCDM 218 and to understand the relationship between its structure and function. For this reason, we determined its glycerol phosphate-substituted structure, which consists of glucose, galactose, and rhamnose residues creating the following repeating unit: To fully understand the role of glycerol phosphate substitution on the B.PAT function, we prepared the dephosphorylated counterpart (B.MAT) and tested their immunomodulatory properties. The results showed that the loss of glycerol phosphate increased the production of IL-6, IL-10, IL-12, and TNF-α in bone marrow dendritic cells alone and after treatment with Lacticaseibacillus rhamnosus GG. Further studies indicated that dephosphorylation can enhance B.PAT properties to suppress IL-1β-induced inflammatory response in Caco-2 and HT-29 cells. Thus, we suggest that further investigation of B.PAT and B.MAT may reveal distinct functionalities that can be exploited in the treatment of various diseases and may constitute an alternative to probiotics.
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