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SRX8984406: GSM4735795: EoE-02.tRNA.EoE; Homo sapiens; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 4.5M spots, 249.2M bases, 47.5Mb downloads

Submitted by: NCBI (GEO)
Study: Conserved interferon signature between adult and pediatric eosinophilic esophagitis
show Abstracthide Abstract
Eosinophilic esophagitis (EoE) is an allergic inflammatory disease of the esophagus that occurs in both children and adults. Previous studies of affected tissue in pediatric cohorts have identified prominent signatures of eosinophilia and type 2 inflammation. However, the details of the immune response in adults with EoE are still being elucidated. To determine whether EoE in adults shares inflammatory profiles with those observed in children, we performed RNA-sequencing of paired esophageal biopsies and blood samples from adults with EoE or gastroesophageal reflux disease (GERD). Unbiased analysis of differentially expressed genes in tissue revealed a strong interferon signature that was significantly enriched in EoE patients as compared to patients with GERD. Both type I and type II interferon responsive genes were upregulated in adult biopsies, but not in blood. A similar increase in expression of interferon gene sets was observed in pediatric EoE biopsies as compared to non-EoE samples, and in public pediatric and adult RNA-sequencing data. Finally, we found that peripheral CD4+ T cells from children with EoE produce IFNG upon activation with EoE-causal allergens. Together, this work identifies a conserved interferon signature in pediatric and adult EoE, highlighting a role for non-type 2 inflammatory networks in the disease process. Overall design: 20 samples total. 10 patients; 4 control, 5 eosinophilic esophagitis, 1 lymphocytic esophagitis. For each patient, an esophageal tissue sample and a blood sample were taken.
Sample: EoE-02.tRNA.EoE
SAMN15878153 • SRS7238726 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Total RNA was isolated from adult esophageal biopsies (1-2 per subject) by homogenizing tissue in QIAzol lysis reagent (Qiagen) followed by column purification using the miRNeasy kit with on column DNA digestion (Qiagen). Whole blood RNA was extracted using MagMax for Stabilized Blood Tubes RNA Isolation Kit, followed by globin reduction using GlobinClear Human (Thermo Fisher). Sequencing libraries were constructed from total RNA using the SMART-Seq v4 Ultra Low Input RNA Kit for Sequencing (Takara) and NexteraXT DNA sample preparation kit (Illumina) to generate Illumina- compatible barcoded libraries. Dual-index, single-read sequencing of pooled libraries was carried out on a HiSeq2500 sequencer (Illumina) with 58-base reads, using HiSeq v4 Cluster and SBS kits (Illumina) with a target depth of 5 million reads per sample.
Experiment attributes:
GEO Accession: GSM4735795
Links:
Runs: 1 run, 4.5M spots, 249.2M bases, 47.5Mb
Run# of Spots# of BasesSizePublished
SRR124928734,491,641249.2M47.5Mb2020-08-23

ID:
11678893

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