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pmid:26981372

Microarray expression analysis of genes involved in innate immune memory in peritoneal macrophages.

Keisuke Yoshida · Claire Renard-Guillet · Kentaro Inoue · Katsuhiko Shirahige · Mariko Okada-Hatakeyama · Shunsuke Ishii

Genomics data · 2016 doi:10.1016/j.gdata.2015.11.028

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title
Microarray expression analysis of genes involved in innate immune memory in peritoneal macrophages.
doi
10.1016/j.gdata.2015.11.028
pmid
26981372
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Keisuke Yoshida
[1]
Claire Renard-Guillet
[2]
Kentaro Inoue
[3]
Katsuhiko Shirahige
[4]
Mariko Okada-Hatakeyama
[5]
Shunsuke Ishii
journal
Genomics data
year
2016
abstract
Immunological memory has been believed to be a feature of the adaptive immune system for long period, but recent reports suggest that the innate immune system also exhibits memory-like reaction. Although evidence of innate immune memory is accumulating, no in vivo experimental data has clearly implicated a molecular mechanism, or even a cell-type, for this phenomenon. In this study of data deposited into Gene Expression Omnibus (GEO) under GSE71111, we analyzed the expression profile of peritoneal macrophages isolated from mice pre-administrated with toll-like receptor (TLR) ligands, mimicking pathogen infection. In these macrophages, increased expression of a group of innate immunity-related genes was sustained over a long period of time, and these genes overlapped with ATF7-regulated genes. We conclude that ATF7 plays an important role in innate immune memory in macrophages.
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Briefly, after a log2 transformation of the signal, a linear model was fitted to each sample to assess variability, and comparisons of groups of interest were made using the empirical Bayes test.
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Briefly, after a log2 transformation of the signal, a linear model was fitted to each sample to assess variability, and comparisons of groups of interest were made using the empirical Bayes test.
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Using limma with Benjamini–Hochberg correction on GEO dataset GSE71111, the study found that 43.6% of LPS-induced DEGs were regulated by ATF7, supporting the conclusion that ATF7 plays an important role in innate immune memory in macrophages.
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A significant fraction of the LPS-induced DEGs was regulated by ATF7 (43.6%, 51/117, chi-square test, P = 9.9 × 10− 158).
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A significant fraction of the LPS-induced DEGs was regulated by ATF7 (43.6%, 51/117, chi-square test, P = 9.9 × 10− 158).
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We conclude that ATF7 plays an important role in innate immune memory in macrophages.
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Comparison of the expression levels was then performed using the R package ‘limma’ [3].
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ATF7 mediates lipopolysaccharide-induced epigenetic changes in macrophages involved in innate immunological memory (expression)
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's instructions. Statistical analysis of the microarray data sets The raw data (CEL file) were first
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Although evidence of innate immune memory is accumulating, no in vivo experimental data has clearly implicated a molecular mechanism, or even a cell-type, for this phenomenon. In this study of data deposited into Gene Expression Omnibus (GEO) under GSE71111, we analyzed the expression profile of peritoneal macrophages isolated from mice pre-administrated with toll-like receptor (TLR) ligands, mimicking pathogen infection. In these macrophages, increased expression of a group of innate immunity-related genes was sustained over a long period of time, and these genes overlapped with ATF7-regulated genes. 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