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dc.contributor.authorButton, RW
dc.contributor.authorLuo, Shouqing
dc.date.accessioned2018-03-20T09:25:27Z
dc.date.issued2017-08-18
dc.identifier.issn1554-8627
dc.identifier.issn1554-8635
dc.identifier.urihttp://hdl.handle.net/10026.1/11111
dc.descriptionpeerreview_statement: The publishing and review policy for this title is described in its Aims & Scope. aims_and_scope_url: http://www.tandfonline.com/action/journalInformation?show=aimsScope&journalCode=kaup20
dc.description.abstract

Macroautophagy/autophagy comprises autophagosome synthesis and lysosomal degradation. It is well known that lysosomal defects cause toxicity to cells. However, it has not been investigated previously if cytotoxicity is conferred by autophagosome formation during lysosomal defect. Recently, we found that the formation of autophagosomes in such conditions also causes cytotoxicity, in addition to lysosomal defect insults. We revealed that a partial reduction in autophagosome synthesis was beneficial for cell survival in cells bearing the autophagosome formation-based toxicity. Our study suggests that production/accumulation of autophagosomes during lysosomal defect directly induces cellular toxicity, and this process may be implicated in the pathological conditions where lysosomes are defective.

dc.format.extent1-2
dc.format.mediumPrint-Electronic
dc.languageen
dc.language.isoen
dc.publisherInforma UK Limited
dc.subjectMTOR
dc.subjectSTX17
dc.subjectautophagosome
dc.subjectautophagy
dc.subjectcytotoxicity
dc.subjectAnimals
dc.subjectAutophagosomes
dc.subjectAutophagy
dc.subjectCell Death
dc.subjectCell Survival
dc.subjectGene Knockdown Techniques
dc.subjectHumans
dc.subjectLysosomes
dc.subjectOrganelle Biogenesis
dc.subjectQa-SNARE Proteins
dc.subjectTOR Serine-Threonine Kinases
dc.titleThe formation of autophagosomes during lysosomal defect: A new source of cytotoxicity
dc.typejournal-article
dc.typeJournal Article
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/28820297
plymouth.issue10
plymouth.volume13
plymouth.publication-statusPublished
plymouth.journalAutophagy
dc.identifier.doi10.1080/15548627.2017.1358850
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/Peninsula Medical School
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)/CBR
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
plymouth.organisational-group/Plymouth/Users by role/Researchers in ResearchFish submission
dc.publisher.placeUnited States
dcterms.dateAccepted2017-07-18
dc.rights.embargodate2018-8-18
dc.identifier.eissn1554-8635
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1080/15548627.2017.1358850
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2017-08-18
rioxxterms.typeJournal Article/Review
plymouth.funderTackling autophagy and apoptosis for the potential therapy of Huntington's Disease::MRC


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