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GEO help: Mouse over screen elements for information. |
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Status |
Public on Mar 22, 2018 |
Title |
β2→1-fructans modulate the immune system in vivo in a microbiota-dependent and -independent fashion |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
It has been shown in vitro that only specific dietary-fibers contribute to immunity but studies in vivo are not conclusive. Here we investigated degree of polymerization (DP) dependent effects of β2→1-fructans on immunity via microbiota-dependent and -independent effects. To this end, conventional or germ-free mice received short- or long-chain β2→1-fructan for 5 days. Immune cell populations in the spleen, mesenteric lymph nodes (MLN), and Peyer's patches (PPs) were analyzed with flow cytometry, genome-wide gene expression in the ileum was measured with microarray, and gut microbiota composition was analyzed with 16S rRNA sequencing of fecal samples. We found that β2→1-fructans modulated immunity by both microbiota and microbiota-independent effects. Moreover, effects were dependent on the chain-length of the β2→1-fructans type polymer. Both short- and long-chain β2→1-fructans enhanced T-helper 1 cells in Peyer's patches, whereas only short-chain β2→1-fructans increased regulatory T cells and CD11b-CD103- DCs in the MLN. A common feature after short- and long-chain β2→1-fructan treatment was enhanced Fut2 expression and other IL-22-dependent genes in the ileum of conventional mice. These effects were not associated with shifts in gut microbiota composition, or altered production of short-chain fatty acids. Both short- and long-chain β2→1-fructans also induced immune effects in germ-free animals, demonstrating direct effect independent from the gut microbiota. Also, these effects were dependent on the chain-length of the β2→1-fructans. Short-chain β2→1-fructan induced lower CD80 expression by CD11b-CD103- DCs in PPs, whereas long-chain β2→1-fructan specifically modulated B cell responses in germ-free mice. In conclusion, support of immunity is determined by the chemical structure of β2→1-fructans and is partially microbiota-independent.
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Overall design |
Conventional or germ-free mice received short-chain (oligofructose; FOS) or long-chain (inulin; IN) β2→1-fructan for 5 days. Genome-wide gene expression in the ileum was measured with microarray.
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Contributor(s) |
Fransen F, Sahasrabudhe N, Elderman M, Bosveld M, El Aidy S, Hugenholtz F, Borghuis T, Kousemaker B, Winkel S, van der Gaast-de Jongh C, de Jonge MI, Boekschoten MV, Smidt H, Schols HA, de Vos P |
Citation(s) |
28261212 |
Submission date |
Feb 03, 2017 |
Last update date |
Mar 24, 2018 |
Contact name |
Guido Hooiveld |
E-mail(s) |
guido.hooiveld@wur.nl
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Organization name |
Wageningen University
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Department |
Div. Human Nutrition & Health
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Lab |
Nutrition, Metabolism & Genomics Group
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Street address |
HELIX, Stippeneng 4
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City |
Wageningen |
ZIP/Postal code |
NL-6708WE |
Country |
Netherlands |
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Platforms (1) |
GPL11533 |
[MoGene-1_1-st] Affymetrix Mouse Gene 1.1 ST Array [transcript (gene) version] |
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Samples (24)
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Relations |
BioProject |
PRJNA371228 |
Supplementary file |
Size |
Download |
File type/resource |
GSE94516_RAW.tar |
104.9 Mb |
(http)(custom) |
TAR (of CEL) |
Processed data included within Sample table |
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