|
Status |
Public on May 12, 2016 |
Title |
Injury-induced enhancer remodelling in spinal microglia - a novel mechanism for pain chronification? [RNA-Seq] |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
|
Summary |
Chronic pain is common and devastating. Yet, its precise molecular origins remain unclear. The condition induces well-characterised changes in neurons and microglia, but it is unknown why they persist long after the precipitating injury has healed. We posit a role for enhancers - regions of open chromatin that define a cell’s transcription factor binding profile. Enhancer profiles can alter upon environmental stimulation, functioning as a kind of molecular memory. Here, a mouse model of persistent neuropathic pain was used to examine microglial enhancers with flow cytometry and sequencing. We observed injury-specific alterations of enhancers in close proximity to transcriptionally regulated genes. Our data also shine light on details relating to the spinal cord immune response and provide the first genome-wide gene expression profile of isolated microglia in a pain state. We hypothesise that enhancer deposition may constitute a novel mechanism by which painful experiences are encoded on a molecular level.
|
|
|
Overall design |
ChIP-seq and RNA-seq of isolated spinal cord microglia after peripheral spinal nerve ligation or sham surgery in mice (day 7)
|
|
|
Contributor(s) |
Denk F, Crow M, Didangelos A, Lopes DM, McMahon SB |
Citation(s) |
27184839 |
|
Submission date |
Jul 21, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Franziska Denk |
Organization name |
King's College London
|
Street address |
Guy's Campus
|
City |
London |
ZIP/Postal code |
SE1 1UL |
Country |
United Kingdom |
|
|
Platforms (1) |
GPL17021 |
Illumina HiSeq 2500 (Mus musculus) |
|
Samples (8)
|
|
This SubSeries is part of SuperSeries: |
GSE71136 |
Injury-induced enhancer remodelling in spinal microglia - a novel mechanism for pain chronification? |
|
Relations |
BioProject |
PRJNA290437 |
SRA |
SRP061355 |