Calpain-mediated cleavage of Fbxw7 during excitotoxicity
DC Field | Value | Language |
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dc.contributor.author | Ko, Yeon Uk | - |
dc.contributor.author | Song, Hwa Young | - |
dc.contributor.author | Kim, Won-Ki | - |
dc.contributor.author | Yune, Tae Young | - |
dc.contributor.author | Yun, Nuri | - |
dc.contributor.author | Oh, Young J. | - |
dc.date.accessioned | 2021-08-30T13:58:47Z | - |
dc.date.available | 2021-08-30T13:58:47Z | - |
dc.date.created | 2021-06-18 | - |
dc.date.issued | 2020-09-25 | - |
dc.identifier.issn | 0304-3940 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/53107 | - |
dc.description.abstract | Neuronal cell death induced by ischemic injury has been attributed to glutamate receptor-mediated excitotoxicity, which is known to be accompanied by Ca2+ overload in the cytoplasm with concomitant activation of calcium-dependent mechanisms. More specifically, the overactivation of calpains, calcium-dependent cysteine proteases, have been associated with neuronal cell death following glutamate treatment. Previously, we observed decreased expression levels of F-box/WD repeat domain-containing protein 7 (Fbxw7) after the hyperactivation of cyclin-dependent kinase 5 (Cdk5) in cortical neurons challenged with glutamate. As determined using in vitro calpain cleavage assays, we demonstrated that the cleavage of Fbxw7 was mediated by activated calpain and attenuated in the presence of the calpain inhibitor, calpeptin. Using the rat middle cerebral artery occlusion model, we confirmed that Fbxw7 was indeed cleaved by activated calpain in the ipsilateral cortex. Based on our data, we hypothesize that the negative regulation of Fbxw7 by calpain may contribute to neuronal cell death and that the preservation of Fbxw7 by the inhibition of calpain, Cdk5, or both composes a novel protective mechanism following excitotoxicity. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | ELSEVIER IRELAND LTD | - |
dc.subject | FBW7 UBIQUITIN LIGASE | - |
dc.subject | TUMOR-SUPPRESSOR | - |
dc.subject | MOLECULAR-MECHANISMS | - |
dc.subject | ISCHEMIC BRAIN | - |
dc.subject | PHOSPHORYLATION | - |
dc.subject | INJURY | - |
dc.subject | NEUROPROTECTION | - |
dc.subject | INHIBITION | - |
dc.subject | PROMOTES | - |
dc.subject | PATHWAY | - |
dc.title | Calpain-mediated cleavage of Fbxw7 during excitotoxicity | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Kim, Won-Ki | - |
dc.identifier.doi | 10.1016/j.neulet.2020.135265 | - |
dc.identifier.scopusid | 2-s2.0-85088400992 | - |
dc.identifier.wosid | 000572426200006 | - |
dc.identifier.bibliographicCitation | NEUROSCIENCE LETTERS, v.736 | - |
dc.relation.isPartOf | NEUROSCIENCE LETTERS | - |
dc.citation.title | NEUROSCIENCE LETTERS | - |
dc.citation.volume | 736 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Neurosciences & Neurology | - |
dc.relation.journalWebOfScienceCategory | Neurosciences | - |
dc.subject.keywordPlus | FBW7 UBIQUITIN LIGASE | - |
dc.subject.keywordPlus | TUMOR-SUPPRESSOR | - |
dc.subject.keywordPlus | MOLECULAR-MECHANISMS | - |
dc.subject.keywordPlus | ISCHEMIC BRAIN | - |
dc.subject.keywordPlus | PHOSPHORYLATION | - |
dc.subject.keywordPlus | INJURY | - |
dc.subject.keywordPlus | NEUROPROTECTION | - |
dc.subject.keywordPlus | INHIBITION | - |
dc.subject.keywordPlus | PROMOTES | - |
dc.subject.keywordPlus | PATHWAY | - |
dc.subject.keywordAuthor | Flucw7 | - |
dc.subject.keywordAuthor | Cleavage | - |
dc.subject.keywordAuthor | Calpain | - |
dc.subject.keywordAuthor | Glutamate | - |
dc.subject.keywordAuthor | Excitotoxicity | - |
dc.subject.keywordAuthor | Middle cerebral artery occlusion (MCAO) | - |
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