Aging alters the molecular dynamics of synapses in a sexually dimorphic pattern in zebrafish (Danio rerio)

buir.contributor.authorKaroglu, Elif Tugce
buir.contributor.authorHalim, Dilara Ozge
buir.contributor.authorErkaya, Bahriye
buir.contributor.authorAltaytas, Ferda
buir.contributor.authorArslan-Ergul, Ayca
buir.contributor.authorKonu, Ozlen
buir.contributor.authorAdams, Michelle M.
dc.citation.epage21
dc.citation.spage10
dc.citation.volumeNumber54
dc.contributor.authorKaroglu, Elif Tugce
dc.contributor.authorHalim, Dilara Ozge
dc.contributor.authorErkaya, Bahriye
dc.contributor.authorAltaytas, Ferda
dc.contributor.authorArslan-Ergul, Ayca
dc.contributor.authorKonu, Ozlen
dc.contributor.authorAdams, Michelle M.
dc.date.accessioned2018-04-12T11:10:54Z
dc.date.available2018-04-12T11:10:54Z
dc.date.issued2017-06
dc.departmentDepartment of Molecular Biology and Genetics
dc.departmentDepartment of Psychology
dc.departmentInstitute of Materials Science and Nanotechnology (UNAM)
dc.departmentInterdisciplinary Program in Neuroscience (NEUROSCIENCE)
dc.departmentAysel Sabuncu Brain Research Center (BAM)
dc.description.abstractThe zebrafish has become a popular model for studying normal brain aging due to its large fecundity, conserved genome, and available genetic tools; but little data exists about neurobiological age-related alterations. The current study tested the hypothesis of an association between brain aging and synaptic protein loss across males and females. Western blot analysis of synaptophysin (SYP), a presynaptic vesicle protein, and postsynaptic density-95 (PSD-95) and gephyrin (GEP), excitatory and inhibitory postsynaptic receptor-clustering proteins, respectively, was performed in young, middle-aged, and old male and female zebrafish (Danio rerio) brains. Univariate and multivariate analyses demonstrated that PSD-95 significantly increased in aged females and SYP significantly decreased in males, but GEP was stable. Thus, these key synaptic proteins vary across age in a sexually dimorphic manner, which has been observed in other species, and these consequences may represent selective vulnerabilities for aged males and females. These data expand our knowledge of normal aging in zebrafish, as well as further establish this model as an appropriate one for examining human brain aging.
dc.identifier.doi10.1016/j.neurobiolaging.2017.02.007
dc.identifier.issn0197-4580
dc.identifier.urihttp://hdl.handle.net/11693/37350
dc.language.isoEnglish
dc.publisherElsevier
dc.relation.isversionofhttps://doi.org/10.1016/j.neurobiolaging.2017.02.007
dc.source.titleNeurobiology of Aging
dc.subjectAging
dc.subjectExcitatory synapses
dc.subjectGender
dc.subjectInhibitory synapses
dc.subjectSynaptic proteins
dc.subjectZebrafish
dc.subjectBeta tubulin
dc.subjectGephyrin
dc.subjectPostsynaptic density protein 95
dc.subjectSynaptophysin
dc.subjectCarrier protein
dc.subjectGephyrin
dc.subjectMembrane protein
dc.subjectSAP90/PSD95 associated protein
dc.subjectsynaptophysin
dc.subjectAdult
dc.subjectAged
dc.subjectAnimal tissue
dc.subjectBrain level
dc.subjectControlled study
dc.subjectJuvenile animal
dc.subjectNonhuman
dc.subjectProtein analysis
dc.subjectProtein depletion
dc.subjectProtein expression
dc.subjectProtein function
dc.subjectProtein localization
dc.subjectSequence homology
dc.subjectSex difference
dc.subjectSynaptic transmission
dc.subjectWestern blotting
dc.subjectZebra fish
dc.subjectAnalysis of variance
dc.subjectAnimal
dc.subjectAnimal model
dc.subjectBrain
dc.subjectGenetics
dc.subjectHuman
dc.subjectMetabolism
dc.subjectPhysiology
dc.subjectSexual characteristics
dc.subjectSynapse
dc.subjectBrain
dc.subjectCarrier Proteins
dc.subjectSAP90-PSD95 Associated Proteins
dc.subjectSex Characteristics
dc.subjectSynapses
dc.subjectSynaptophysin
dc.titleAging alters the molecular dynamics of synapses in a sexually dimorphic pattern in zebrafish (Danio rerio)
dc.typeArticle

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