Bcl-2 affects survival but not neuronal differentiation of PC12 cells

dc.contributor.authorBatistatou, A.en
dc.contributor.authorMerry, D. E.en
dc.contributor.authorKorsmeyer, S. J.en
dc.contributor.authorGreene, L. A.en
dc.date.accessioned2015-11-24T19:33:22Z
dc.date.available2015-11-24T19:33:22Z
dc.identifier.issn0270-6474-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/23529
dc.rightsDefault Licence-
dc.subjectAnimalsen
dc.subjectBlotting, Northernen
dc.subjectBlotting, Westernen
dc.subjectCell Differentiation/drug effects/*physiologyen
dc.subjectCell Survival/drug effects/*physiologyen
dc.subjectHumansen
dc.subjectKineticsen
dc.subjectNerve Growth Factors/pharmacologyen
dc.subjectNeurons/*cytology/metabolismen
dc.subjectPC12 Cellsen
dc.subjectProtein-Tyrosine Kinases/metabolismen
dc.subjectProto-Oncogene Proteins/analysis/biosynthesis/*metabolismen
dc.subjectProto-Oncogene Proteins c-bcl-2en
dc.subject*Proto-Oncogenesen
dc.subjectRNA/analysisen
dc.subjectRNA, Messenger/biosynthesis/metabolismen
dc.subjectRecombinant Proteins/analysis/biosynthesis/metabolismen
dc.subjectTime Factorsen
dc.subjectTransfectionen
dc.titleBcl-2 affects survival but not neuronal differentiation of PC12 cellsen
heal.abstractPast studies have shown that serum-free cultures of PC12 cells are a useful model system for studying the mechanisms of neuronal death after neurotrophic factor deprivation. These cultures, as well as NGF-deprived cultures of sympathetic neurons, manifest and endonuclease activity that leads to "apoptotic" internucleosomal DNA cleavage. Overexpression of the proto-oncogene bcl-2 blocks apoptotic death in various cell types. To study the actions of this protein in neuronal cells, we derived PC12 cell lines stably transfected with a cDNA encoding human bcl-2. It is reported here that lines expressing high levels of the exogenous bcl-2 protein are protected from both death and apoptotic DNA fragmentation caused by removal of trophic support. However, expression of high levels of exogenous bcl-2 neither mimics nor interferes with promotion of neurite outgrowth by NGF.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/7692014-
heal.journalNameJ Neuroscien
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate1993-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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