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Series GSE200309 Query DataSets for GSE200309
Status Public on Aug 08, 2022
Title Differential gene expression in iPSC-derived human intestinal epithelial cell layers following exposure to two concentrations of the Short Chain Fatty Acids butyrate, propionate and acetate
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Intestinal epithelial cells and the intestinal microbiota are in a mutualistic relationship that is dependent on communication. This communication is multifaceted, but one aspect is communication through compounds produced by the microbiota such as the short-chain fatty acids (SCFAs) butyrate, propionate and acetate. Studying the effects of SCFAs and especially butyrate in intestinal epithelial cell lines like Caco-2 cells has been proven problematic. In contrast to the in vivo intestinal epithelium, Caco-2 cells do not use butyrate as an energy source, leading to a build-up of butyrate. Therefore, we used human induced pluripotent stem cell derived intestinal epithelial cells, grown as a cell layer, to study the effects of butyrate, propionate and acetate on whole genome gene expression in the cells. For this, cells were exposed to concentrations of 1 and 10 mM of the individual short-chain fatty acids for 24 hours. Unique gene expression profiles were observed for each of the SCFAs in a concentration-dependent manner. Evaluation on both an individual gene level and pathway level showed that butyrate induced the biggest effects followed by propionate and then acetate. Several known effects of SCFAs on intestinal cells were confirmed, such as effects on metabolism and immune responses. The changes in metabolic pathways in the intestinal epithelial cell layers in this study demonstrate that there is a switch in energy source from glucose to SCFAs, thus induced pluripotent stem cell derived intestinal epithelial cell are responding in a similar manner to SCFAs as in vivo intestinal tissues.
 
Overall design Induced pluripotent stem cell derived intestinal epithelial cells were exposed to butyric acid (NaB; 1 or 10mM), acetic acid (NaA 1 or 10 mM), propionic acid, (NaP 1 or 10 mM) or control treatment (water) for 24 hours, and subjected to gene expression profiling by RNA-sequencing.
 
Contributor(s) Grouls M, Janssen AF, Duivenvoorde LM, Hooiveld GJ, Bouwmeester H, van de Zande M
Citation(s) 35977967
Submission date Apr 06, 2022
Last update date Aug 26, 2022
Contact name Menno Grouls
E-mail(s) menno.grouls@outlook.com
Organization name Wageningen University & Research
Department Toxicology
Street address Postbus 8000
City Wageningen
ZIP/Postal code 6700 EA
Country Netherlands
 
Platforms (1)
GPL23227 BGISEQ-500 (Homo sapiens)
Samples (21)
GSM6030852 iPSC IEC, butyrate 1 mM treatment, replicate 1
GSM6030853 iPSC IEC, butyrate 1 mM treatment, replicate 2
GSM6030854 iPSC IEC, butyrate 1 mM treatment, replicate 3
Relations
BioProject PRJNA824040

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Supplementary file Size Download File type/resource
GSE200309_TxImport.GeneLevel.counts.GEO.txt.gz 1.5 Mb (ftp)(http) TXT
GSE200309_txi.counts.annotated.GEO.Rdata.gz 14.2 Mb (ftp)(http) RDATA
GSE200309_txi.lengthScaledTPM.annotated.GEO.Rdata.gz 16.6 Mb (ftp)(http) RDATA
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Raw data are available in SRA
Processed data are available on Series record

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