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http://doi.org/10.25358/openscience-3120Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Starossom, Sarah-Christin | |
| dc.date.accessioned | 2011-08-03T10:21:05Z | |
| dc.date.available | 2011-08-03T12:21:05Z | |
| dc.date.issued | 2011 | |
| dc.identifier.uri | https://openscience.ub.uni-mainz.de/handle/20.500.12030/3122 | - |
| dc.description.abstract | Inflammation-mediated neurodegeneration occurs in the acute and the chronic/progressive phases of multiple sclerosis (MS) and its animal model experimental autoimmune encephalomyelitis (EAE). Classically-activated microglia (M1) are key players mediating this process through secretion of soluble factors including nitric oxide (NO) and tumor necrosis factor (TNF). Here, galectin-1, an endogenous glycan-binding protein, was identified as a pivotal regulatory mechanism that limits M1 microglia activation and neurodegeneration, by targeting the activation of p38MAPK- and CREB-dependent pathways and hierarchically controlling downstream pro-inflammatory mediators such as iNOS, TNF and CCL2. Galectin-1 is highly expressed in the acute phase of EAE and its targeted deletion results in pronounced inflammation-induced neurodegeneration. These findings identify an essential role of galectin-1-glycan lattices in tempering microglia activation, brain inflammation and neurodegeneration with critical therapeutic implications in relapsing-remitting and secondary progressive MS.rnMicroglia with distinct phenotypes are implicated in neurotoxicity, neuroprotection, and in modulation of endogenous repair by NSCs. However the precise molecular mechanisms underlying this diversity in fuction are still unknown. rnUsing a model of EAE, transcriptional profiling of isolated SVZ microglia from the acute and chronic disease phases of EAE was performed. The results from this study suggest that microglia exhibit disease phase specific gene expression signatures, that correspond to unique GO functions and genomic networks. These data demonstrate for the first time, distinct transcriptional networks of microglia activation in vivo, that support their role as mediators of injury or repair. | en_GB |
| dc.language.iso | eng | |
| dc.rights | InCopyright | de_DE |
| dc.rights.uri | https://rightsstatements.org/vocab/InC/1.0/ | |
| dc.subject.ddc | 500 Naturwissenschaften | de_DE |
| dc.subject.ddc | 500 Natural sciences and mathematics | en_GB |
| dc.title | The role of microglia in neurodegeneration and endogenous repair during experimental autoimmune encephalomyelitis | en_GB |
| dc.type | Dissertation | de_DE |
| dc.identifier.urn | urn:nbn:de:hebis:77-28014 | |
| dc.identifier.doi | http://doi.org/10.25358/openscience-3120 | - |
| jgu.type.dinitype | doctoralThesis | |
| jgu.type.version | Original work | en_GB |
| jgu.type.resource | Text | |
| jgu.organisation.department | FB 10 Biologie | - |
| jgu.organisation.year | 2011 | |
| jgu.organisation.number | 7970 | - |
| jgu.organisation.name | Johannes Gutenberg-Universität Mainz | - |
| jgu.rights.accessrights | openAccess | - |
| jgu.organisation.place | Mainz | - |
| jgu.subject.ddccode | 500 | |
| opus.date.accessioned | 2011-08-03T10:21:05Z | |
| opus.date.modified | 2011-08-18T09:08:49Z | |
| opus.date.available | 2011-08-03T12:21:05 | |
| opus.subject.dfgcode | 00-000 | |
| opus.organisation.string | FB 10: Biologie: Abteilung Molekulare Zellbiologie / Biologie für Mediziner | de_DE |
| opus.identifier.opusid | 2801 | |
| opus.institute.number | 1004 | |
| opus.metadataonly | false | |
| opus.type.contenttype | Dissertation | de_DE |
| opus.type.contenttype | Dissertation | en_GB |
| jgu.organisation.ror | https://ror.org/023b0x485 | |
| Appears in collections: | JGU-Publikationen | |
