scholarly journals Human milk oligosaccharides alter the intestinal epithelial cell surface glycome: A proof‐of‐principle

2010 ◽  
Vol 24 (S1) ◽  
Author(s):  
Kathrin Straubinger ◽  
Milady Ninonuevo ◽  
Lars Bode
Keyword(s):  
Epithelial Cell ◽  
Cell Surface ◽  
Human Milk ◽  
Intestinal Epithelial Cell ◽  
Intestinal Epithelial ◽  
Human Milk Oligosaccharides ◽  
Milk Oligosaccharides ◽  
Epithelial Cell Surface ◽  
Proof Of Principle

Intestinal Epithelial Cell Surface Glycosylation in Mice

1992 ◽  
Vol 36 (2) ◽  
pp. 71-78 ◽  
Author(s):  
Reena Gupta ◽  
Virender M.S. Jaswal ◽  
Akhtar Mahmood
Keyword(s):  
Epithelial Cell ◽  
Cell Surface ◽  
Intestinal Epithelial Cell ◽  
Intestinal Epithelial ◽  
Epithelial Cell Surface

Human Milk Oligosaccharides Attenuate Antigen-Antibody Complex Induced Chemokine Release from Human Intestinal Epithelial Cell Lines

2018 ◽  
Vol 83 (2) ◽  
pp. 499-508 ◽  
Author(s):  
Sehrish Zehra ◽  
Ibrahim Khambati ◽  
Megan Vierhout ◽  
M. Firoz Mian ◽  
Rachael Buck ◽  
...  
Keyword(s):  
Epithelial Cell ◽  
Human Milk ◽  
Cell Lines ◽  
Intestinal Epithelial Cell ◽  
Intestinal Epithelial ◽  
Human Milk Oligosaccharides ◽  
Human Intestinal Epithelial Cell ◽  
Epithelial Cell Lines ◽  
Antibody Complex ◽  
Antigen Antibody

Intestinal Epithelial Cell Surface Glycosylation in Mice

1992 ◽  
Vol 36 (5-6) ◽  
pp. 288-295 ◽  
Author(s):  
Reena Gupta ◽  
Virender M.S. Jaswal ◽  
Meenu Akhtar Mahmood
Keyword(s):  
Epithelial Cell ◽  
Cell Surface ◽  
Intestinal Epithelial Cell ◽  
Intestinal Epithelial ◽  
Epithelial Cell Surface

scholarly journals Human milk oligosaccharides and non-digestible carbohydrates prevent adhesion of specific pathogens via modulating glycosylation or inflammatory genes in intestinal epithelial cells

2021 ◽  
Author(s):  
Chunli Kong ◽  
Martin Beukema ◽  
Min Wang ◽  
Bart J. de Haan ◽  
Paul de Vos
Keyword(s):  
Epithelial Cells ◽  
Human Milk ◽  
Intestinal Epithelial Cells ◽  
Intestinal Epithelial ◽  
Human Milk Oligosaccharides ◽  
Milk Oligosaccharides ◽  
Inflammatory Genes

Human milk oligosaccharides 2′-FL and pectins inhibited pathogen adhesion through modulating glycosylation and inflammatory genes in intestinal epithelial cells.

scholarly journals Protective Effects of Human Milk Oligosaccharides on Intestinal Epithelial Function Assessed in Enteroid‐Derived Monolayers

2018 ◽  
Vol 32 (S1) ◽  
Author(s):  
Alice Drobny ◽  
Stella Rita Ibeawuchi ◽  
Soumita Das ◽  
Lars Bode ◽  
Kim Elaine Barrett
Keyword(s):  
Human Milk ◽  
Protective Effects ◽  
Intestinal Epithelial ◽  
Human Milk Oligosaccharides ◽  
Milk Oligosaccharides

scholarly journals Human Milk Oligosaccharides Mediate the Crosstalk Between Intestinal Epithelial Caco-2 Cells and Lactobacillus PlantarumWCFS1in an In Vitro Model with Intestinal Peristaltic Shear Force

2020 ◽  
Vol 150 (8) ◽  
pp. 2077-2088 ◽  
Author(s):  
Chunli Kong ◽  
Lianghui Cheng ◽  
Guido Krenning ◽  
Jolien Fledderus ◽  
Bart J de Haan ◽  
...  
Keyword(s):  
Gene Expression ◽  
Epithelial Cells ◽  
Tight Junction ◽  
Human Milk ◽  
Shear Force ◽  
Intestinal Epithelial Cells ◽  
Intestinal Epithelial ◽  
Human Milk Oligosaccharides ◽  
Commensal Bacterium ◽  
Milk Oligosaccharides

ABSTRACT Background The intestinal epithelial cells, food molecules, and gut microbiota are continuously exposed to intestinal peristaltic shear force. Shear force may impact the crosstalk of human milk oligosaccharides (hMOs) with commensal bacteria and intestinal epithelial cells. Objectives We investigated how hMOs combined with intestinal peristaltic shear force impact intestinal epithelial cells and crosstalk with a commensal bacterium. Methods We applied the Ibidi system to mimic intestinal peristaltic shear force. Caco-2 cells were exposed to a shear force (5 dynes/cm2) for 3 d, and then stimulated with the hMOs, 2′-fucosyllactose (2′-FL), 3-FL, and lacto-N-triose II (LNT2). In separate experiments, Lactobacillus plantarumWCFS1 adhesion to Caco-2 cells was studied with the same hMOs and shear force. Effects were tested on gene expression of glycocalyx-related molecules (glypican 1 [GPC1], hyaluronan synthase 1 [HAS1], HAS2, HAS3, exostosin glycosyltransferase 1 [EXT1], EXT2), defensin β-1 (DEFB1), and tight junction (tight junction protein 1 [TJP1], claudin 3 [CLDN3]) in Caco-2 cells. Protein expression of tight junctions was also quantified. Results Shear force dramatically decreased gene expression of the main enzymes for making glycosaminoglycan side chains (HAS3 by 43.3% and EXT1 by 68.7%) (P <0.01), but did not affect GPC1 which is the gene responsible for the synthesis of glypican 1 which is a major protein backbone of glycocalyx. Expression of DEFB1, TJP1, and CLDN3 genes was decreased 60.0–94.9% by shear force (P <0.001). The presence of L. plantarumWCFS1 increased GPC1, HAS2, HAS3, and ZO-1 expression by 1.78- to 3.34-fold (P <0.05). Under shear force, all hMOs significantly stimulated DEFB1 and ZO-1, whereas only 3-FL and LNT2 enhanced L. plantarumWCFS1 adhesion by 1.85- to 1.90-fold (P <0.01). Conclusions 3-FL and LNT2 support the crosstalk between the commensal bacterium L. plantarumWCFS1 and Caco-2 intestinal epithelial cells, and shear force can increase the modulating effects of hMOs.

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