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| Status |
Public on Jan 25, 2019 |
| Title |
IL-6 trans-signaling induced gene expression in airway epithelial cells |
| Organism |
Homo sapiens |
| Experiment type |
Expression profiling by high throughput sequencing
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| Summary |
Background: Although several studies link high levels of IL-6 and soluble IL-6 receptor (sIL-6R) with asthma severity and decreased lung function, the role of IL-6 trans-signaling (IL-6TS) in asthma is unclear.
Objective: To explore the association between epithelial IL-6TS pathway activation and molecular and clinical phenotypes in asthma.
Methods: Primary human bronchial epithelial cell (HBEC) air-liquid interface (ALI) cultures were stimulated with IL-6 and sIL-6R to establish an IL-6TS gene signature. Two separate RNA sequencing (RNA-seq) studies were performed: The “IL-6 vs T2 study” compared gene expression after stimulation with control medium, IL-6, IL-6/sIL-6R and IL-4/IL-13, while the “JAK1-inhibition study” addressed the effect of JAK1 inhibition on IL-6TS induced gene expression. The IL-6TS gene signature was used to stratify lung epithelial transcriptomic data obtained from asthmatics (n=103) in the U-BIOPRED cohorts by hierarchical clustering. Molecular phenotyping was based on the transcriptional profiling of epithelial brushings, pathway analysis and immunohistochemistry analysis of bronchial biopsies.
Results: Activation of IL-6TS in HBEC ALI cultures reduced epithelial barrier function and induced a specific epithelial gene signature enriched in airway remodeling genes. The IL-6TS signature identified a subset (n=17) of IL-6TS High asthma patients with increased epithelial expression of IL-6TS inducible genes in absence of increased systemic levels of IL-6 and sIL-6R. The IL-6TS High subset had an increased exacerbation frequency (p=0.028), blood (>300/μl; p=0.0028) and sputum (>20%; p=0.007) eosinophilia, and submucosal infiltration of CD4 T cells, CD8 T cells (p<0.001) and macrophages (p=0.001). In bronchial brushings, TLR pathway genes were up-regulated while the expression of epithelial tight junction genes was reduced (all with q<0.05). Sputum sIL-6R levels correlated with sputum markers of remodeling and innate immune activation, in particular YKL-40, MMP3, IL-8 and IL-1β (all with q<0.001).
Conclusions: Local lung epithelial IL-6TS activation in absence of type 2 airway inflammation defines a novel subset of asthmatics and may drive airway inflammation and epithelial dysfunction in these patients.
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| Overall design |
Primary human bronchial epithelial cells grown and differentiated on air-liquid interface were stimulated basolaterally for 24h with cytokines corresponding to IL-6TS (IL-6 + sIL-6R), IL-6 alone, a Type 2 immune response (IL-4 + IL-13) or media alone as non-stimulated control. Each stimulation condition was done in triplicates. Cells were lysed, the RNA isolated and converted into libraries then used for next generation sequencing in order to identify genes that were up- or downregulated in response to the different stimulations.
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| Web link |
http://10.1016/j.jaci.2018.05.026
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| Contributor(s) |
Jevnikar Rojnik Z, Ax E, Thörn K, Israelsson E, Öberg L, Olsson HK |
| Citation(s) |
29902480 |
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| Submission date |
Apr 16, 2018 |
| Last update date |
Mar 26, 2019 |
| Contact name |
Elisabeth Israelsson |
| E-mail(s) |
[email protected]
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| Organization name |
AstraZeneca, IMED RIA
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| Department |
Translational Biology
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| Street address |
Pepparedsleden 1
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| City |
Molndal |
| ZIP/Postal code |
SE-431 83 |
| Country |
Sweden |
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| Platforms (1) |
| GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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| Samples (24)
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| Relations |
| BioProject |
PRJNA450389 |
| SRA |
SRP140515 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE113185_Study1_combined.counts.txt.gz |
704.9 Kb |
(ftp)(http) |
TXT |
| GSE113185_Study1_combined.gene.sf.tpm.txt.gz |
1.6 Mb |
(ftp)(http) |
TXT |
| GSE113185_Study2_combined.counts.txt.gz |
655.9 Kb |
(ftp)(http) |
TXT |
| GSE113185_Study2_combined.gene.sf.tpm.txt.gz |
1.6 Mb |
(ftp)(http) |
TXT |
SRA Run Selector |
| Raw data are available in SRA |
| Processed data are available on Series record |
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