Mechanisms of Synapse Formation and Synaptic Plasticity

atmire.migration.oldid3042
dc.contributor.advisorSyed, Naweed
dc.contributor.authorLuk, Collin Chill-Fone
dc.date.accessioned2015-04-06T21:16:25Z
dc.date.available2015-06-22T07:00:39Z
dc.date.issued2015-04-06
dc.date.submitted2015en
dc.description.abstractSynapses are the fundamental building blocks of the nervous system. Following target cell contact, they are formed through a process that requires the precise orchestration of both pre- and postsynaptic differentiation of synaptic machinery. However, the precise time course of synaptogenesis, and the role of extrinsic factors in synapse formation remains unclear. To examine the time course of synaptogenesis, I developed a novel “growth ball” model to study synapse at the level of isolated growth cones. Specifically, I found that functional synapses can reform in isolated growth cones within minutes of contact with their synaptic partner. However, in the absence of the cell body, these synapses cannot be maintained. To further investigate the importance of the cell body, I demonstrate that extrinsic trophic factors can “prime” postsynaptic neurons for synapse formation through the functional expression of excitatory acetylcholine receptors via activity dependent mechanisms. Specifically, trophic factor induced activity follows a specific pattern of progression, which I termed an activity “signature”, that is necessary for proper expression of excitatory acetylcholine receptors. Finally, I demonstrate and characterize a novel form of use-dependent short-term potentiation that is observed in the visceral dorsal 1/left pedal dorsal 1 synapse. This synaptic plasticity is induced rapidly by a short presynaptic tetanic pulse and remains potentiated until a subsequent action potential is triggered in a use- rather than time-dependent manner. I show that the molecular switch underlying this form of potentiation is calcium/calmodulin kinase II (CaMKII). Taken together, these studies demonstrate both intrinsic and extrinsic mechanisms of synapse formation and identify a novel role for CaMKII in a use-dependent form of synaptic plasticity.en_US
dc.identifier.citationLuk, C. C. (2015). Mechanisms of Synapse Formation and Synaptic Plasticity (Doctoral thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca. doi:10.11575/PRISM/26867en_US
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/26867
dc.identifier.urihttp://hdl.handle.net/11023/2131
dc.language.isoeng
dc.publisher.facultyGraduate Studies
dc.publisher.institutionUniversity of Calgaryen
dc.publisher.placeCalgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.
dc.subjectNeuroscience
dc.subject.classificationSynaptogenesisen_US
dc.subject.classificationTrophic factorsen_US
dc.subject.classificationGrowth conesen_US
dc.subject.classificationShort-term potentiationen_US
dc.titleMechanisms of Synapse Formation and Synaptic Plasticity
dc.typedoctoral thesis
thesis.degree.disciplineNeuroscience
thesis.degree.grantorUniversity of Calgary
thesis.degree.nameDoctor of Philosophy (PhD)
ucalgary.item.requestcopytrue
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