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Status |
Public on Dec 17, 2015 |
Title |
Expression response of human monocyte derived macrophages to dexamethasone over a 24h time series |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
Macrophages are amongst the major targets of glucocorticoids (GC) as therapeutic anti-inflammatory agents. Here we show that GC treatment of mouse and human macrophages initiates a cascade of induced gene expression including many anti-inflammatory genes. Inducible binding of the glucocorticoid receptor (GR) was detected at candidate enhancers in the vicinity of induced genes in both species and this was strongly associated with canonical GR binding motifs. However, the sets of inducible genes, the candidate enhancers, and the GR motifs within them, were highly-divergent between the two species.. The data cast further doubt upon the predictive value of mouse models of inflammatory disease.
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Overall design |
Four biological replicates of a 6 point 24h time series transcriptional response of human monocyte derived macrophages to dexamethasone 100nM.
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Contributor(s) |
Jubb AW, Bickmore WA, Hume DA, Young RS |
Citation(s) |
26663721, 29241532 |
Submission date |
Sep 29, 2014 |
Last update date |
Jul 15, 2019 |
Contact name |
Alasdair W Jubb |
E-mail(s) |
alasdair.jubb@ed.ac.uk
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Organization name |
University of Edinburgh
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Department |
Roslin Institute
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Lab |
Hume lab / Bickmore lab (MRC HGU)
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Street address |
The Roslin Institute
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City |
Easter Bush |
State/province |
Midlothian |
ZIP/Postal code |
EH25 9RG |
Country |
United Kingdom |
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Platforms (1) |
GPL13158 |
[HT_HG-U133_Plus_PM] Affymetrix HT HG-U133+ PM Array Plate |
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Samples (24)
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This SubSeries is part of SuperSeries: |
GSE61881 |
Divergent transcriptional activation by glucocorticoids in mouse and human macrophages is the result of gain and loss of enhancers |
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Relations |
BioProject |
PRJNA262587 |