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Susumu Tonegawa. Murphy, Alexander J. (Alexander James) Massachusetts Institute of Technology. Dept. of Nuclear Science and Engineering. Massachusetts Institute of Technology. Department of Nuclear Science and Engineering 2011-05-09T15:21:59Z 2011-05-09T15:21:59Z 2010 2010 http://hdl.handle.net/1721.1/62699 714584858 Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Nuclear Science and Engineering, 2010. Cataloged from PDF version of thesis. Includes bibliographical references (p. 34-36). Based on extracellular field recordings and stimulations at the Schaeffer collateral-CA1 synapse, the synaptic tagging and capture (STC) model has hypothesized that at synapses that express any form of LTP and LTD (long-term potentiation and depression, respectively) are tagged in a protein synthesis-independent manner, the induction of LLTP/ L-LTD leads to protein synthesis, and all tagged synapses can use the resulting plasticity-related products to express L-LTP/L-LTD. Several models have hypothesized that STC works through somatically synthesized plasticity-related protein products available to synapses throughout the neuron, suggesting that, at the single neuronal level, memory engrams are formed at synapses throughout the dendritic arbor. However, the Clustered Plasticity Hypothesis suggests that neurons store long-term memory engrams at synapses that tend to be spatially clustered within dendritic branches, as opposed to dispersed throughout the dendritic arbor. This hypothesis suggests that the dendritic branch, as opposed to the synapse, is the primary unit for long-term memory storage. Evidence for this hypothesis has come from studies of LTP, however, and there is no such data for LTD. This thesis establishes a single-synapse marker for LTD, namely spine length changes, that can be used to study the role of LTD and dendritic branch-specific plasticity. by Alexander J. Murphy. S.B. 36 p. eng Massachusetts Institute of Technology M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 Nuclear Science and Engineering. Effect of chemically induced mGluR-dependent long-term depression on dendritic spine volume Thesis application/pdf Publication unknown unknown <Publication xmlns="https://www.openaire.eu/cerif-profile/1.1/" id="620acd79-67a9-4720-8af9-86c50484067c"> <Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843</Type> <Language>eng</Language> <Title>Effect of chemically induced mGluR-dependent long-term depression on dendritic spine volume</Title> <PublishedIn> <Publication> </Publication> </PublishedIn> <PublicationDate>2010</PublicationDate> <Authors> <Author> <DisplayName>Murphy, Alexander J. (Alexander James)</DisplayName> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> </Authors> <Editors> </Editors> <Publishers> <Publisher> <DisplayName>Massachusetts Institute of Technology</DisplayName> <OrgUnit /> </Publisher> </Publishers> <License>http://dspace.mit.edu/handle/1721.1/7582</License> <Keyword>Nuclear Science and Engineering.</Keyword> <Abstract>Based on extracellular field recordings and stimulations at the Schaeffer collateral-CA1 synapse, the synaptic tagging and capture (STC) model has hypothesized that at synapses that express any form of LTP and LTD (long-term potentiation and depression, respectively) are tagged in a protein synthesis-independent manner, the induction of LLTP/ L-LTD leads to protein synthesis, and all tagged synapses can use the resulting plasticity-related products to express L-LTP/L-LTD. Several models have hypothesized that STC works through somatically synthesized plasticity-related protein products available to synapses throughout the neuron, suggesting that, at the single neuronal level, memory engrams are formed at synapses throughout the dendritic arbor. However, the Clustered Plasticity Hypothesis suggests that neurons store long-term memory engrams at synapses that tend to be spatially clustered within dendritic branches, as opposed to dispersed throughout the dendritic arbor. This hypothesis suggests that the dendritic branch, as opposed to the synapse, is the primary unit for long-term memory storage. Evidence for this hypothesis has come from studies of LTP, however, and there is no such data for LTD. This thesis establishes a single-synapse marker for LTD, namely spine length changes, that can be used to study the role of LTD and dendritic branch-specific plasticity.</Abstract> <Access xmlns="http://purl.org/coar/access_right" > </Access> </Publication>