Key Features
Enhance your research with our curated data sets and powerful platform features. Pluto Bio makes it simple to find and use the data you need.
Learn MoreThe respective effects of tissue alarmins like interleukin (IL)-15 and interferon beta (IFNb), and cytokines like IL-21 on the intraepithelial cytotoxic T lymphocytes (IE-CTLs) that cause autoimmune-mediated tissue destruction, is poorly understood. Analysis of the dynamics of transcriptomic and epigenomic profiles in primary IE-CTLs showed massive and distinct temporal transcriptional changes upon induction by tissue alarmins IL-15 and IFNb, while the impact of IL-21 was limited. Only anti-viral pathways were induced in response to all the three stimuli. Interestingly, the dynamically differentially expressed genes (DEGs), in particular genes in involved in IFN pathways, are enriched in autoimmune diseases risk loci. Changes in gene expression were primarily independent of changes in H3K27ac, but were enriched in differentially expressed non-coding (nc) RNAs. Together these results provide new insights into molecular mechanisms that fuel the activation of tissue resident CTLs under conditions that mimic aspects of the inflammatory environment in patients with immune-mediated diseases SOURCE: Raul Aguirre-Gamboa (raul.aguirre.gamboa@gmail.com) - Wijmenga Lab University of Groningen, University Medical Center Groningen
View on GEOView in PlutoEnhance your research with our curated data sets and powerful platform features. Pluto Bio makes it simple to find and use the data you need.
Learn MoreUse Pluto's intuitive interface to analyze and visualize data for this experiment. Pluto's platform is equipped with an API & SDKs, making it easy to integrate into your internal bioinformatics processes.
Read about post-pipeline analysisView quality control data and experiment metadata for this experiment.
Request imports from GEO or TCGA directly within Pluto Bio.
Chat with our Scientific Insights team