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Sample GSM1015442 Query DataSets for GSM1015442
Status Public on Apr 23, 2013
Title IRF3/5/7 TKO 6b
Sample type RNA
Source name RPMI + rmGM-CSF purified BM-DC populations, mock and WNV infected with insect derived virus and RNA isolated 24 hours post infection.
Organism Mus musculus
Characteristics subject: Mouse_16
genotype: IRF3/5/7 TKO
cell type: bone marrow derived myeloid DC bmDCs
infection: West Nile Virus
time point: 24 hours
Treatment protocol GM-CSF was replenished after 2 days and non-adherent cells were sub-cultured after 4 days. Sub-cultured cells were infected at an MOI of 25 with WNV-NY. To determine the percentage of cells infected, mDC were detached 24 h after WNV inoculation. Non-specific binding of antibody to Fc-γR was blocked with anti-CD16/CD32 (Biolegend), and all subsequent surface staining (I-Ab-FITC, CD86-PE, and CD11c-APC (all from Biolegend)) was performed in PBS supplemented with 2% fetal calf serum. Cells were fixed, permeabilized, and then stained with Alexa-647 conjugated anti-WNV E16 anti-WNV MAb. For microarray analysis, total RNA was harvested at 24 hours post-infection.
Growth protocol Bone marrow was cultured in RPMI supplemented with 10% fetal bovine serum, penicillin/streptomycin, L-glutamine, non-essential amino acids, 55 μM β-mercaptoethanol and 20 ng/ml recombinant mouse GM-CSF (eBioscience) for 6 days in non-tissue culture treated plates.
Extracted molecule total RNA
Extraction protocol The DC/Mac populations were harvested at each desired post-infection time point. The cells were washed once with RT 1XPBS (about 2ml/Well). Then 0.5ml added of warmed trypsin to each well, incubate 10 min at 37°C. Once this was done, 5 ml added of cold PBS w/ 10% serum or use 10% complete medium. The cells were then collected in 15ml conical tube. Cells were spun down at 1000-1200 RPM x 5 minutes at 4°C.
Label Biotin
Label protocol The hybridized BeadChips were washed, blocked, stained and scanned according to the Illumina's direct hybridization protocol.
Hybridization protocol Microarray analysis was conducted using 750ng of biotinylated cRNA hybridized to Human RefSeq-8 V2 BeadChips (Illumina) at 58°C for 20 hours, according to Illumina's direct hybridization protocol
Scan protocol The arrays were scanned using an Illumina iScan scanner and quantified using GenomeStudio software (Illumina).
Description bmDC from Mouse_16, wnv infected
Data processing Analysis of the GenomeStudio output data was conducted using the R statistical language and various software packages from Bioconductor. Missing values were imputed using the KNN algorithm from the impute R package. Quantile normalization was applied, followed by a log2 transformation
Submission date Oct 04, 2012
Last update date Apr 23, 2013
Contact name Peter A Wilkinson
Organization name Case Western Reserve University
Department Pathology / Systems Biology & Bioinformatics
Street address 2103 Cornell Road
City Cleveland
State/province Ohio
ZIP/Postal code 44120
Country USA
Platform ID GPL6885
Series (1)
GSE41355 IRF-3, IRF-5, and IRF-7 coordinately regulate the type I IFN response in myeloid dendritic cells downstream of MAVS signaling

Data table header descriptions
VALUE Quantile normalized, log2 transformed intensities

Data table
ILMN_1250052 7.315277754
ILMN_3122480 6.920886495
ILMN_2599935 8.123730999
ILMN_2675543 6.955951414
ILMN_2686883 7.379460108
ILMN_2751818 6.872457099
ILMN_2728634 7.209637277
ILMN_3040515 6.697557733
ILMN_2711608 6.897788389
ILMN_1232875 7.799006639
ILMN_1258507 6.955951414
ILMN_2746142 6.860794181
ILMN_1252690 7.184781798
ILMN_2655499 6.824028076
ILMN_1252870 7.011016227
ILMN_1248179 6.710871398
ILMN_2649955 7.583969739
ILMN_2628708 8.021791876
ILMN_3024781 6.886329273
ILMN_2705628 11.3155875

Total number of rows: 25697

Table truncated, full table size 626 Kbytes.

Supplementary file Size Download File type/resource
GSM1015442_6197801007_G_beadTypeFile.txt.gz 168.8 Kb (ftp)(http) TXT
Raw data provided as supplementary file
Processed data included within Sample table
Raw data are available on Series record

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