<HashMap><database>GEO</database><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE313127</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Pharmacological activation of UPR pathways and its impact on gene expression</name><description>This study investigates how pharmacologic activationn of the PERK branch of the unfolded protein response (UPR) enhances the immunoregulatory function of FoxP3⁺ regulatory T cells (Tregs) in the context of intestinal inflammation. Using ER stress-inducing agents and PERK activators, combined with flow cytometry, bulk RNA sequencing, in vitro Treg conversion and suppression assays, ELISA, qRT-PCR, and immunoblotting, we demonstrate that PERK activation reduces gut inflammation and promotes Treg-mediated immune regulation. These findings identify the PERK pathway as a novel immunologic target for enhancing Treg function and mitigating chronic intestinal inflammation, offering translational relevance for therapeutic strategies in inflammatory bowel disease (IBD).</description><dates><publication>2026/05/31</publication></dates><accession>GSE313127</accession><cross_references><GSM>GSM9362383</GSM><GSM>GSM9362382</GSM><GSM>GSM9362387</GSM><GSM>GSM9362386</GSM><GSM>GSM9362385</GSM><GSM>GSM9362384</GSM><GPL>34290</GPL><GSE>313127</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>