Associating structural characteristics to immunomodulating properties of carrot rhamnogalacturonan-I fractions

  • Krishna Desai
  • , Justyna M. Dobruchowska
  • , Kari Elbers
  • , Justyna Cybulska
  • , Artur Zdunek
  • , Mojtaba Porbahaie
  • , Erik Jansen
  • , Joost Van Neerven
  • , Ruud Albers
  • , Tom Wennekes
  • , Annick Mercenier
  • , Henk A. Schols*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Carrot rhamnogalacturonan-I (cRG-I) is a polydisperse polysaccharide with molecular weights of 7–250 kDa. Using size exclusion chromatography cRG-I was fractionated and pooled in fractions (PF1–6). All fractions contained the same RG-I monosaccharides and similar glycosidic linkages although in varying relative amounts. The main differences were in rhamnose substitution, arabinan- and galactan side chain length and in levels of acetylation and methyl esterification. Atomic force microscopy showed either spheric or elongated structures for cRG-I and its derived fractions. To gain insight in the structure-function relationship of cRG-I, the immunomodulatory effect of the six fractions and their saponified derivatives was assessed in vitro. All fractions, except PF2, dose-dependently stimulated TNFα, IL-6, IL-1β, IL-8 and IL-10 production in peripheral blood mononuclear cells (PBMCs) of three healthy donors. Cytokine levels were largely influenced by the Mw and degree of esterification of the individual fractions. Notably, the highest Mw fraction (100 kDa) displayed the most potent activity, which was strongly reduced after the removal of ester residues by saponification. In contrast, the 75 kDa Mw population (PF2) proved inactive while its saponified counterpart exhibited substantial immunomodulatory activity. This confirmed the role of ester residues on the immune profile of RG-I subpopulations.

Original languageEnglish
Article number122730
Number of pages13
JournalCarbohydrate Polymers
Volume347
DOIs
Publication statusPublished - 1 Jan 2025

Bibliographical note

Publisher Copyright:
© 2024 The Authors

Funding

This research has received funding from the European Union's Horizon 2020 research and innovation programme as part of funding Programme Marie Sklodowska-Curie ITN 2018 under grant agreement No 814102.

FundersFunder number
European Union814102

    Keywords

    • Acetylated pectic polysaccharides
    • Immunomodulation
    • Rhamnogalacturonan
    • Saponification
    • Size fractionation
    • Structural characterization
    • Structure-function activity

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