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Series GSE41731 Query DataSets for GSE41731
Status Public on Jan 01, 2013
Title HIV downregulates interferon stimulated genes in primary macrophages.
Organism Homo sapiens
Experiment type Expression profiling by array
Summary HIV is able to outpace the innate immune response, including the response mediated by interferon (IFN), to establish a productive infection. However, monocyte derived macrophages (MDMs) may be protected from HIV infection by treatment with type I IFN before virus exposure. The ability of HIV to modulate the type I IFN-mediated innate immune response when it encounters a cell that has already been exposed to IFN was investigated.
 
Overall design To investigate the presence of HIV on an established IFN response, MDMs were subjected to four different conditions: (1) IFN-treated only, (2) IFN-treated followed by HIV infection, (3) HIV infected only, and (4) a mock-treated and mock-infected control. Microarray gene expression analysis was performed on a total of 24 samples derived from the 4 conditions assessed at 3 time points (1, 4 and 8 days following treatment/infection) for both IFN-α2 or -ω. Initially, ISGs were identified as those that were upregulated greater than 2-fold by IFN alone (condition 1) at both Days 4 and 8. Then, the IFN-treated condition was compared to the IFN-treated followed by HIV-infection condition in order to identify those ISGs that were downregulated at least 1.5-fold by the presence of HIV at both days. Assuming that it would be counterproductive for HIV infection by itself to induce the expression of ISGs with putative anti-HIV effects, those ISGs that were upregulated greater than 2-fold in the HIV control were removed. Finally, ISGs that passed these filters and were concordant with both IFN-treatments (IFN-α2 and -ω) were identified and corresponded to the following 8 ISGs: AXL receptor tyrosine kinase (AXL), interferon-alpha inducible protein 27 (IFI27), interferon-induced protein 44 (IFI44), interferon-induced protein 44-like (IFI44L), ISG15, OAS1, OAS3 and XIAP associated factor 1 (XAF1). It should be noted that the IFN-α2 and -ω microarray experiments were performed in different batches but batch effects were not corrected since genes were identified by the filtering approach just described within each batch.
 
Contributor(s) Wie S, Singhania A, Woelk CH
Citation(s) 23276142
Submission date Oct 19, 2012
Last update date Feb 18, 2019
Contact name Akul Singhania
E-mail(s) akul.singhania@crick.ac.uk
Phone +442037963319
Organization name The Francis Crick Institute
Street address 1 Midland Road
City London
ZIP/Postal code NW1 1AT
Country United Kingdom
 
Platforms (1)
GPL6884 Illumina HumanWG-6 v3.0 expression beadchip
Samples (24)
GSM1023331 MDMA2_D1
GSM1023332 HIVA2_D4
GSM1023333 IFNA2_D8
Relations
BioProject PRJNA178033

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE41731_4254964012.sdf.gz 3.3 Kb (ftp)(http) SDF
GSE41731_4254964024.sdf.gz 3.3 Kb (ftp)(http) SDF
GSE41731_4312191006.sdf.gz 3.3 Kb (ftp)(http) SDF
GSE41731_4312191012.sdf.gz 3.3 Kb (ftp)(http) SDF
GSE41731_4313143153.sdf.gz 3.3 Kb (ftp)(http) SDF
GSE41731_4313143154.sdf.gz 3.3 Kb (ftp)(http) SDF
GSE41731_RAW.tar 62.5 Mb (http)(custom) TAR (of IDAT)
GSE41731_non-normalized.txt.gz 16.9 Mb (ftp)(http) TXT
Processed data included within Sample table

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