Calpain-mediated cleavage of Fbxw7 during excitotoxicity

Yeon Uk Ko, Hwa Young Song, Won Ki Kim, Tae Young Yune, Nuri Yun, Young J. Oh

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2 Citations (Scopus)


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.

Original languageEnglish
Article number135265
JournalNeuroscience Letters
Publication statusPublished - 2020 Sept 25

Bibliographical note

Funding Information:
This work was supported by the Small Grant for Exploratory Research program (2018R1D1A1A02085731 to NY) through the National Research Foundation of Korea (NRF) grant funded by Ministry of Education and by the Brain Research Program (2017M37A1025369 to YJO) and by the Mid-Career Research Program (2019R1A2C1088793 to YJO) through the NRF grant funded by Ministry of Science and ICT.

Publisher Copyright:
© 2020 Elsevier B.V.

All Science Journal Classification (ASJC) codes

  • Neuroscience(all)


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