E-MTAB-1615 - Transcription profiling by array of PUFA-treated rats to better understand the mechanisms of miRNAs in PUFA-modulated cellular pathways

Released on 22 April 2013, last updated on 3 June 2014
Rattus norvegicus
Samples (9)
Array (1)
Protocols (6)
To better understand the mechanisms of miRNAs in PUFA-modulated cellular pathways, we compared physical signs and immune statuses of PUFA-treated rats. The results indicated that omega-3 PUFAs decreased production of pro-inflammatory cytokines such as interleukin-6, C-reactive protein, and tumor necrosis factor-a, at the same time, increased proportion of CD8+ suppressor T cells and regulatory T cells in rats. The changes of these biological parameters showed that the PUFA diet-induced autoimmune (AI)-prone and AI-averse rat models were successfully established. As following steps, differentially expressed miRNAs were filtered in peripheral serum by microarray assay and validated in PBMC, liver, visceral fat, and pituitary gland by stem-loop real-time quantitative-PCR (RT-qPCR). Biological databases and computational algorithms were used to classify the potential target genes of these PUFA-induced differentially expressed miRNAs.
Experiment types
transcription profiling by array, co-expression, compound treatment design, in vivo
PUFA diets alter the microRNA expression profiles in an inflammation rat model. Zheng Z, Ge Y, Zhang J, Xue M, Li Q, Lin D, Ma W. :4149-4157 (2015), Europe PMC 25672643
Investigation descriptionE-MTAB-1615.idf.txt
Sample and data relationshipE-MTAB-1615.sdrf.txt
Raw data (1)E-MTAB-1615.raw.1.zip
Array designA-MEXP-2004.adf.txt