Phosphorylation-dependent immunomodulatory properties of B.PAT polysaccharide isolated from Bifidobacterium animalis ssp. animalis CCDM 218
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
39218543
DOI
10.1016/j.carbpol.2024.122518
PII: S0144-8617(24)00744-6
Knihovny.cz E-zdroje
- Klíčová slova
- Bifidobacterium, Dephosphorylation, Immunomodulation, Polysaccharides, Postbiotics, Surface antigens,
- MeSH
- bakteriální polysacharidy farmakologie chemie izolace a purifikace MeSH
- Bifidobacterium animalis * chemie MeSH
- buňky HT-29 MeSH
- Caco-2 buňky MeSH
- cytokiny metabolismus MeSH
- dendritické buňky účinky léků imunologie metabolismus MeSH
- fosforylace účinky léků MeSH
- imunologické faktory farmakologie chemie izolace a purifikace MeSH
- Lacticaseibacillus rhamnosus chemie MeSH
- lidé MeSH
- myši MeSH
- probiotika farmakologie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- bakteriální polysacharidy MeSH
- cytokiny MeSH
- imunologické faktory 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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