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dc.contributor.authorWali, Gautam
dc.contributor.authorLiyanage, Erandhi
dc.contributor.authorBlair, Nicholas F
dc.contributor.authorSutharsan, Ratneswary
dc.contributor.authorPark, Jin-Sung
dc.contributor.authorMackay-Sim, Alan
dc.contributor.authorSue, Carolyn M
dc.date.accessioned2020-09-11T05:19:23Z
dc.date.available2020-09-11T05:19:23Z
dc.date.issued2020
dc.identifier.issn1662-4548
dc.identifier.doi10.3389/fnins.2020.00401
dc.identifier.urihttp://hdl.handle.net/10072/397403
dc.description.abstractHereditary spastic paraplegia (HSP) is a group of inherited disorders characterized by progressive spasticity and paralysis of the lower limbs. Autosomal dominant mutations in SPAST gene account for ∼40% of adult-onset patients. We have previously shown that SPAST patient cells have reduced organelle transport and are therefore more sensitive to oxidative stress. To test whether these effects are present in neuronal cells, we first generated 11 induced pluripotent stem (iPS) cell lines from fibroblasts of three healthy controls and three HSP patients with different SPAST mutations. These cells were differentiated into FOXG1-positive forebrain neurons and then evaluated for multiple aspects of axonal transport and fragmentation. Patient neurons exhibited reduced levels of SPAST encoded spastin, as well as a range of axonal deficits, including reduced levels of stabilized microtubules, lower peroxisome transport speed as a consequence of reduced microtubule-dependent transport, reduced number of peroxisomes, and higher density of axon swellings. Patient axons fragmented significantly more than controls following hydrogen peroxide exposure, suggesting for the first time that the SPAST patient axons are more sensitive than controls to the deleterious effects of oxidative stress. Treatment of patient neurons with tubulin-binding drugs epothilone D and noscapine rescued axon peroxisome transport and protected them against axon fragmentation induced by oxidative stress, showing that SPAST patient axons are vulnerable to oxidative stress-induced degeneration as a consequence of reduced axonal transport.
dc.description.peerreviewedYes
dc.languageEnglish
dc.language.isoeng
dc.publisherFrontiers Media SA
dc.relation.ispartofpagefrom401
dc.relation.ispartofjournalFrontiers in Neuroscience
dc.relation.ispartofvolume14
dc.subject.fieldofresearchNeurosciences
dc.subject.fieldofresearchPsychology
dc.subject.fieldofresearchCognitive Sciences
dc.subject.fieldofresearchcode1109
dc.subject.fieldofresearchcode1701
dc.subject.fieldofresearchcode1702
dc.subject.keywordsScience & Technology
dc.subject.keywordsLife Sciences & Biomedicine
dc.subject.keywordshereditary spastic paraplegia
dc.subject.keywordsNeurology
dc.titleOxidative Stress-Induced Axon Fragmentation Is a Consequence of Reduced Axonal Transport in Hereditary Spastic Paraplegia SPAST Patient Neurons
dc.typeJournal article
dc.type.descriptionC1 - Articles
dcterms.bibliographicCitationWali, G; Liyanage, E; Blair, NF; Sutharsan, R; Park, J-S; Mackay-Sim, A; Sue, CM, Oxidative Stress-Induced Axon Fragmentation Is a Consequence of Reduced Axonal Transport in Hereditary Spastic Paraplegia SPAST Patient Neurons, Frontiers in Neuroscience, 2020, 14, pp. Frontiers in Neuroscience
dcterms.dateAccepted2020-04-01
dcterms.licensehttp://creativecommons.org/licenses/by/4.0/
dc.date.updated2020-09-11T05:16:47Z
dc.description.versionVersion of Record (VoR)
gro.rights.copyright© 2020 Wali, Liyanage, Blair, Sutharsan, Park, Mackay-Sim and Sue. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
gro.hasfulltextFull Text
gro.griffith.authorMackay-Sim, Alan
gro.griffith.authorSutharsan, Ratneswary


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