E-GEOD-44333 - Analysis of the host transcriptome from demyelinating spinal cord of murine coronavirus infected mice

Released on 15 June 2013, last updated on 4 July 2013
Mus musculus
Samples (2)
Protocols (4)
We use transcriptome analysis to study the spinal cord transcriptome during MHV-induced demyelinating disease and find important biological pathways for demyelinating pathology. We find evidence of a Th1 cytokine response, ongoing antigen presentation and lymphocyte proliferation, lipid metabolism changes, and eicosanoid inflammation. In addition, we report several genes important for osteoclast function have augmented expression in the CNS during demyelination, suggesting a parallel between the osteoclast and microglial functions in maintaining homeostasis and the fidelity of specialized extracellular matrices in their respective compartments. RNA-seq of mock-infected and MHV-infected spinal cord tissue at 33 days post-infection, the peak of demyelination.
Experiment type
RNA-seq of coding RNA 
Megan Ruth Elliott <melli@upenn.edu>, Ruth Elliott, Susan R Weiss
Exp. designProtocolsVariablesProcessedSeq. reads
Investigation descriptionE-GEOD-44333.idf.txt
Sample and data relationshipE-GEOD-44333.sdrf.txt
Additional data (1)E-GEOD-44333.additional.1.zip