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Series GSE115282 Query DataSets for GSE115282
Status Public on Jan 28, 2020
Title Transcriptional regulation of Th17 differentiation by mitochondrial oxidative phosphorylation
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary We found that mitochondrial oxidative phosphorylation (OXPHOS) plays a critical role in Th17 lineage specification. CD4 T cells differentiated under OXPHOS inhibited conditions show altered metabolic gene profiles (mitochondrial function, glycolysis, and TCA cycle) and pathways associated with cell proliferation. Furthermore, gene set enrichment analysis (GSEA) revealed that mitochondrial respiration impacts transcriptional profiles related to Th17 pathogenic signatures and BATF-sensitive gene clusters. Our study reveals a regulatory role of mitochondrial OXPHOS in transcriptional programming of Th17 lineage commitment.
 
Overall design Naïve CD4 T cells were differentiated into Th17 cells in the presence of vehicle (DMSO) or oligomycin (OXPHOS inhibitor) for 48 hours. Total mRNA profiles were generated by RNA sequencing in triplicate.
 
Contributor(s) Shin B, Benavides GA, Geng J, Hu H, Darley-Usmar VM, Koralov SB, Harrington LE
Citation(s) 32049019
Submission date Jun 04, 2018
Last update date May 01, 2020
Contact name Boyoung Shin
E-mail(s) boyoung@caltech.edu
Organization name Californial Institute of Technology
Street address 1200 E. California Blvd
City Pasadena
State/province California
ZIP/Postal code 91125
Country USA
 
Platforms (1)
GPL17021 Illumina HiSeq 2500 (Mus musculus)
Samples (6)
GSM3173575 17-DMSO
GSM3173576 17-Oligo
GSM3173577 42-DMSO
Relations
BioProject PRJNA474475
SRA SRP149688

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE115282_LEH_OXPHOS_dataset.txt.gz 441.2 Kb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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