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Series GSE167274 Query DataSets for GSE167274
Status Public on Feb 23, 2021
Title Microglia contributes to remyelination in cerebral but not spinal cord ischemia
Organism Mus musculus
Experiment type Expression profiling by array
Summary Inflammation after injury of the central nervous system (CNS) is increasingly viewed as a therapeutic target. However, comparative studies in different CNS compartments are sparse. To date only few studies based on immunohistochemical data and all referring to mechanical injury have directly compared inflammation in different CNS compartments. These studies revealed that inflammation is more pronounced in spinal cord than in brain. Therefore, it is unclear whether concepts and treatments established in the cerebral cortex can be transferred to spinal cord lesions and vice versa or whether immunological treatments must be adapted to different CNS compartments. By use of transcriptomic and flow cytometry analysis of equally sized photothrombotically induced lesions in the cerebral cortex and the spinal cord, we could document an overall comparable inflammatory reaction and repair activity in brain and spinal cord between day 1 and day 7 after ischemia. However, remyelination was increased after cerebral versus spinal cord ischemia which is in line with increased remyelination in grey matter in previous analyses and was accompanied by microglia dominated inflammation opposed to monocytes/macrophages dominated inflammation after spinal cord ischemia. Interestingly remyelination could be reduced by microglia and not hematogenous macrophage depletion.
Our results show that despite different cellular composition of the postischemic infiltrate the inflammatory response in cerebral cortex and spinal cord are comparable between day 1 and day 7. A striking difference was higher remyelination capacity in the cerebral cortex, which seems to be supported by microglia dominance.
 
Overall design 32 total samples were analyzed
 
Contributor(s) Pavic G, Petzsch P, Jansen R, Raba K, Rychlik N, Simiantonakis I, Küry P, Göttle P, Köhrer K, Hartung H, Meuth SG, Jander S, Gliem M
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Submission date Feb 22, 2021
Last update date Feb 26, 2021
Contact name Goran Pavic
E-mail(s) goran.pavic@med.uni-duesseldorf.de
Organization name Universitätsklinikum Düsseldorf
Department Neurologische Klinik
Street address Moorenstrasse 5
City Düsseldorf
State/province NRW
ZIP/Postal code 40225
Country Germany
 
Platforms (1)
GPL23038 [Clariom_S_Mouse] Affymetrix Clariom S Assay, Mouse (Includes Pico Assay)
Samples (32)
GSM5100701 G1929
GSM5100702 G1930
GSM5100703 G1931
Relations
BioProject PRJNA704037

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

Supplementary file Size Download File type/resource
GSE167274_RAW.tar 40.9 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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