Metabolomics,Multiomics

Dataset Information

0

A microfluidics-based in vitro model of the gastrointestinal human-microbe interface


ABSTRACT: Changes in the human gastrointestinal microbiome are associated with several diseases. To infer causality, experiments in representative models are essential, but widely used animal models exhibit limitations. Here we present a modular, microfluidics-based model (HuMiX, human–microbial crosstalk), which allows co-culture of human and microbial cells under conditions representative of the gastrointestinal human–microbe interface. We demonstrate the ability of HuMiX to recapitulate in vivo transcriptional, metabolic and immunological responses in human intestinal epithelial cells following their co-culture with the commensal Lactobacillus rhamnosus GG (LGG) grown under anaerobic conditions. In addition, we show that the co-culture of human epithelial cells with the obligate anaerobe Bacteroides caccae and LGG results in a transcriptional response, which is distinct from that of a co-culture solely comprising LGG. HuMiX facilitates investigations of host–microbe molecular interactions and provides insights into a range of fundamental research questions linking the gastrointestinal microbiome to human health and disease.

OTHER RELATED OMICS DATASETS IN: PXD013655PRJNA315665

INSTRUMENT(S): 5975C Series GC/MSD (Agilent)

SUBMITTER: Christian Jaeger 

PROVIDER: MTBLS328 | MetaboLights | 2017-07-28

REPOSITORIES: MetaboLights

Dataset's files

Source:
Action DRS
MTBLS328 Other
FILES Other
a_MTBLS328_humix_metabolite_profiling_mass_spectrometry.txt Txt
i_Investigation.txt Txt
m_MTBLS328_humix_metabolite_profiling_mass_spectrometry_v2_maf.tsv Tabular
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Publications


Changes in the human gastrointestinal microbiome are associated with several diseases. To infer causality, experiments in representative models are essential, but widely used animal models exhibit limitations. Here we present a modular, microfluidics-based model (HuMiX, human-microbial crosstalk), which allows co-culture of human and microbial cells under conditions representative of the gastrointestinal human-microbe interface. We demonstrate the ability of HuMiX to recapitulate in vivo transcr  ...[more]

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