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dc.contributor.authorZhang, Xuen_US
dc.contributor.authorZhou, Jian-Yingen_US
dc.contributor.authorH. Chin, Marken_US
dc.contributor.authorA. Schepmoes, Athenaen_US
dc.contributor.authorA. Petyuk, Vladislaven_US
dc.contributor.authorK. Weitz, Karlen_US
dc.contributor.authorO. Petritis, Brianneen_US
dc.contributor.authorE. Monroe, Matthewen_US
dc.contributor.authorG. Camp II, Daviden_US
dc.contributor.authorWood, Stephenen_US
dc.contributor.authorP. Melega, Williamen_US
dc.contributor.authorJ. Bigelow, Dianaen_US
dc.contributor.authorJ. Smith, Desmonden_US
dc.contributor.authorQian, Wei-Junen_US
dc.contributor.authorD. Smith, Richarden_US
dc.date.accessioned2017-04-24T11:03:43Z
dc.date.available2017-04-24T11:03:43Z
dc.date.issued2010en_US
dc.date.modified2011-03-07T08:51:52Z
dc.identifier.issn1535-3893en_US
dc.identifier.doi10.1021/pr901024zen_AU
dc.identifier.urihttp://hdl.handle.net/10072/36821
dc.description.abstractParkinson's disease (PD) is characterized by dopaminergic neurodegeneration in the nigrostriatal region of the brain; however, the neurodegeneration extends well beyond dopaminergic neurons. To gain a better understanding of the molecular changes relevant to PD, we applied two-dimensional LC-MS/ MS to comparatively analyze the proteome changes in four brain regions (striatum, cerebellum, cortex, and the rest of brain) using a MPTP-induced PD mouse model with the objective to identify potential nigrostriatal-specific and other region-specific protein abundance changes. The combined analyses resulted in the identification of 4,895 nonredundant proteins with at least two unique peptides per protein. The relative abundance changes in each analyzed brain region were estimated based on the spectral count information. A total of 518 proteins were observed with substantial MPTP-induced abundance changes across different brain regions. A total of 270 of these proteins were observed with specific changes occurring either only in the striatum and/or in the rest of the brain region that contains substantia nigra, suggesting that these proteins are associated with the underlying nigrostriatal pathways. Many of the proteins that exhibit changes were associated with dopamine signaling, mitochondrial dysfunction, the ubiquitin system, calcium signaling, the oxidative stress response, and apoptosis. A set of proteins with either consistent change across all brain regions or with changes specific to the cortex and cerebellum regions were also detected. Ubiquitin specific protease (USP9X), a deubiquination enzyme involved in the protection of proteins from degradation and promotion of the TGF- pathway, exhibited altered abundance in all brain regions. Western blot validation showed similar spatial changes, suggesting that USP9X is potentially associated with neurodegeneration. Together, this study for the first time presents an overall picture of proteome changes underlying both nigrostriatal pathways and other brain regions potentially involved in MPTP-induced neurodegeneration. The observed molecular changes provide a valuable reference resource for future hypothesis-driven functional studies of PD.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherAmerican Chemical Societyen_US
dc.publisher.placeUnited Statesen_US
dc.relation.ispartofstudentpublicationNen_AU
dc.relation.ispartofpagefrom1496en_US
dc.relation.ispartofpageto1509en_US
dc.relation.ispartofissue3en_US
dc.relation.ispartofjournalJournal of Proteome Researchen_US
dc.relation.ispartofvolume9en_US
dc.rights.retentionYen_AU
dc.subject.fieldofresearchBiochemistry and Cell Biology not elsewhere classifieden_US
dc.subject.fieldofresearchcode060199en_US
dc.titleRegion-Specific Protein Abundance Changes in the Brain of MPTP-Induced Parkinson’s Disease Mouse Modelen_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.rights.copyrightSelf-archiving of the author-manuscript version is not yet supported by this journal. Please refer to the journal link for access to the definitive, published version or contact the authors for more information.en_AU
gro.date.issued2010
gro.hasfulltextNo Full Text


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