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Carboxypeptidase E cytoplasmic tail mediates localization of synaptic vesicles to the pre-active zone in hypothalamic pre-synaptic terminals

dc.contributor.authorLou, Hongen_US
dc.contributor.authorPark, Joshua J.en_US
dc.contributor.authorCawley, Niamh X.en_US
dc.contributor.authorSarcon, Annahitaen_US
dc.contributor.authorSun, Leien_US
dc.contributor.authorAdams, Tiffanyen_US
dc.contributor.authorPeng Loh, Yokeen_US
dc.date.accessioned2011-01-31T17:35:32Z
dc.date.available2011-10-03T17:19:14Zen_US
dc.date.issued2010-08en_US
dc.identifier.citationLou, Hong; Park, Joshua J.; Cawley, Niamh X.; Sarcon, Annahita; Sun, Lei; Adams, Tiffany; Peng Loh, Yoke; (2010). "Carboxypeptidase E cytoplasmic tail mediates localization of synaptic vesicles to the pre-active zone in hypothalamic pre-synaptic terminals." Journal of Neurochemistry 114(3): 886-896. <http://hdl.handle.net/2027.42/79163>en_US
dc.identifier.issn0022-3042en_US
dc.identifier.issn1471-4159en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/79163
dc.description.abstractJ. Neurochem. (2010) 114 , 886–896.How synaptic vesicles (SVs) are localized to the pre-active zone (5–200 nm beneath the active zone) in the nerve terminal, which may represent the slow response SV pool, is not fully understood. Electron microscopy revealed the number of SVs located in the pre-active zone, was significantly decreased in hypothalamic neurons of carboxypeptidase E knockout (CPE-KO) mice compared with wild-type mice. Additionally, we found K + -stimulated glutamate secretion from hypothalamic embryonic neurons was impaired in CPE-KO mice. Biochemical studies indicate that SVs from the hypothalamus of wild-type mice and synaptic-like microvesicles from PC12 cells contain a transmembrane form of CPE, with a cytoplasmic tail (CPE C10 ), maybe involved in synaptic function. Yeast two-hybrid and pull-down experiments showed that the CPE cytoplasmic tail interacted with γ-adducin, which binds actin enriched at the nerve terminal. Total internal reflective fluorescence (TIRF) microscopy using PC12 cells as a model showed that expression of GFP-CPE C15 reduced the steady-state level of synaptophysin-mRFP containing synaptic-like microvesicles accumulated in the area within 200 nm from the sub-plasma membrane (TIRF zone). Our findings identify the CPE cytoplasmic tail, as a new mediator for the localization of SVs in the actin-rich pre-active zone in hypothalamic neurons and the TIRF zone of PC12 cells.en_US
dc.format.extent539373 bytes
dc.format.extent3106 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.subject.otherActin Cortexen_US
dc.subject.otherCarboxypeptidase Een_US
dc.subject.otherGlutamate Secretionen_US
dc.subject.otherHypothalamic Neuronen_US
dc.subject.otherPC12 Cellsen_US
dc.subject.otherγ-Adducinen_US
dc.titleCarboxypeptidase E cytoplasmic tail mediates localization of synaptic vesicles to the pre-active zone in hypothalamic pre-synaptic terminalsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pharmacology, University of Michigan, School of Medicine, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherSection on Cellular Neurobiology, Program on Developmental Neuroscience, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USAen_US
dc.contributor.affiliationotherDepartment of Neurosciences, University of Toledo, School of Medicine, Toledo, Ohio, USAen_US
dc.identifier.pmid20492353en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/79163/1/j.1471-4159.2010.06820.x.pdf
dc.identifier.doi10.1111/j.1471-4159.2010.06820.xen_US
dc.identifier.sourceJournal of Neurochemistryen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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