*** TEST ***
Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

Distinctive waves of innate immune response in the retina in experimental autoimmune encephalomyelitis

[thumbnail of Original Article]
Preview
PDF (Original Article) - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
2MB
[thumbnail of Supplementary Material]
Preview
PDF (Supplementary Material) - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
139kB

Item Type:Article
Title:Distinctive waves of innate immune response in the retina in experimental autoimmune encephalomyelitis
Creators Name:Cruz-Herranz, A., Oertel, F.C., Kim, K., Cantó, E., Timmons, G., Sin, J.H., Devereux, M., Baker, N., Michel, B., Schubert, R.D., Rani, L., Cordano, C., Baranzini, S.E. and Green, A.J.
Abstract:Neurodegeneration mediates neurological disability in inflammatory demyelinating diseases of the CNS. The role of innate immune cells in mediating this damage has remained controversial with evidence for destructive and protective effects. This has complicated efforts to develop treatment. The time sequence and dynamic evolution of the opposing functions are especially unclear. Given limits of in vivo monitoring in human diseases such as multiple sclerosis (MS), animal models are warranted to investigate the association and timing of innate immune activation with neurodegeneration. Using noninvasive in vivo retinal imaging of experimental autoimmune encephalitis (EAE) in CX3CR1(GFP/+)-knock-in mice followed by transcriptional profiling, we are able to show 2 distinct waves separated by a marked reduction in the number of innate immune cells and change in cell morphology. The first wave is characterized by an inflammatory phagocytic phenotype preceding the onset of EAE, whereas the second wave is characterized by a regulatory, antiinflammatory phenotype during the chronic stage. Additionally, the magnitude of the first wave is associated with neuronal loss. Two transcripts identified - growth arrest-specific protein 6 (GAS6) and suppressor of cytokine signaling 3 (SOCS3) - might be promising targets for enhancing protective effects of microglia in the chronic phase after initial injury.
Keywords:CX3C Chemokine Receptor 1, Disease Progression, Experimental Autoimmune Encephalomyelitis, Freund's Adjuvant, Gene Expression Profiling, Gene Knock-In Techniques, Innate Immunity, Intercellular Signaling Peptides and Proteins, Microglia, Myelin-Oligodendrocyte Glycoprotein, Peptide Fragments, Phagocytosis, Retina, Suppressor of Cytokine Signaling 3 Protein, Animals, Mice
Source:JCI Insight
ISSN:2379-3708
Publisher:American Society for Clinical Investigation
Volume:6
Number:11
Page Range:e149228
Date:8 June 2021
Official Publication:https://doi.org/10.1172/jci.insight.149228
PubMed:View item in PubMed

Repository Staff Only: item control page

Downloads

Downloads per month over past year

Open Access
MDC Library