ArticleBMC biotechnology2025
Interaction of potato-derived RG-I with galectin-3 and gene regulation in human mesenchymal stem cells.
Article in BMC biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
backgroundMesenchymal stem cells (MSC) play a vital role in bone regeneration. Poly-(l-lactide-co-ε-caprolactone) scaffolds functionalised with modified rhamnogalacturonan-I (RG-I) potato pectin, can modulate inflammation and promote bone regeneration in-vitro and in-vivo by modulating the action of the galactoside-binding galectin-3. In this study, we determined the binding affinity to galectin-3 of potato unmodified RG-I (PU) and its arabinose-deficient form (PA) and investigated the transcriptomic effects of PA treatment on human MSCs evaluated through in-silico pathway analysis in relation to galectin-3.
methodsThe binding affinity of RG-I (PU and PA) to galectin-3 was assessed by tryptophan fluorescence spectroscopy. Human MSC (hMSC) isolated from the bone marrow of elderly patients (> 60yrs), were analysed by transcriptomic profiling. The effect of PA surface coating on gene expression was assessed in-silico by the ingenuity pathway analysis (IPA).
resultsRG-I binds to galectin-3 with a binding affinity of 8.66 × 10
conclusionsThis study indicates that modified potato pectin (PA) can regulate the expression of a broad range of genes, including galectin-3, that are involved in cellular, inflammatory, and immunological functions of hMSCs and may potentially be used to promote bone regeneration via modulation of inflammation.
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