2015
DOI: 10.1186/s12864-015-1218-9
|View full text |Cite
|
Sign up to set email alerts
|

Genome-wide immunity studies in the rabbit: transcriptome variations in peripheral blood mononuclear cells after in vitro stimulation by LPS or PMA-Ionomycin

Abstract: BackgroundOur purpose was to obtain genome-wide expression data for the rabbit species on the responses of peripheral blood mononuclear cells (PBMCs) after in vitro stimulation by lipopolysaccharide (LPS) or phorbol myristate acetate (PMA) and ionomycin. This transcriptome profiling was carried out using microarrays enriched with immunity-related genes, and annotated with the most recent data available for the rabbit genome.ResultsThe LPS affected 15 to 20 times fewer genes than PMA-Ionomycin after both 4 hour… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
15
0

Year Published

2016
2016
2023
2023

Publication Types

Select...
8
1

Relationship

3
6

Authors

Journals

citations
Cited by 23 publications
(17 citation statements)
references
References 71 publications
2
15
0
Order By: Relevance
“…We used rabbit-specific gene expression microarray ( Jacquier et al., 2015 ) to analyze the expression of approximately 13,000 genes in CKF-4, CKF-8, AKF-5, AKF-20, AKSL-4, AKSL-8, AKSL-20, AKSF-19, AKSF-26, AKSgff-3, and AKSgff-62 (Gene Ontology accession number GEO: GSE79195 ). Given the inherent instability of CKL cells, they were not included in the transcriptome analysis.…”
Section: Resultsmentioning
confidence: 99%
“…We used rabbit-specific gene expression microarray ( Jacquier et al., 2015 ) to analyze the expression of approximately 13,000 genes in CKF-4, CKF-8, AKF-5, AKF-20, AKSL-4, AKSL-8, AKSL-20, AKSF-19, AKSF-26, AKSgff-3, and AKSgff-62 (Gene Ontology accession number GEO: GSE79195 ). Given the inherent instability of CKL cells, they were not included in the transcriptome analysis.…”
Section: Resultsmentioning
confidence: 99%
“…Total blood RNA (200 ng) was retro-transcribed, Cy3-labeled, and hybridized onto customized single-channel 8X60K Agilent Technologies arrays (platform Agilent-037880/INRA Susscrofa 60K v1), which were enriched in genes linked to immunity and muscle physiology, following the manufacturer’s instructions and a protocol described in Jacquier et al (2015) [ 46 ]. Because genomic sequencing data were not available, it was not possible to take a possible effect of within cDNA target polymorphisms on hybridization levels into account.…”
Section: Methodsmentioning
confidence: 99%
“…One pHu-sample was considered an outlier after the principal component analysis and was thus removed from the analysis. All of the steps of the RNA labelling and microarray processing were performed by the CRB GADIE facility (INRA, UMR GABI, Jouy-en-Josas, France, http://crbgadie.inra.fr/) as described in Jacquier et al 45 . The microarray data were submitted to the Gene Expression Omnibus (GEO) microarray database (accession number GSE89268).…”
Section: Microarray Data Production and Statistical Analysesmentioning
confidence: 99%