Effect of chemically induced mGluR-dependent long-term depression on dendritic spine volume

Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Nuclear Science and Engineering, 2010.

Bibliographic Details
Main Author: Murphy, Alexander J. (Alexander James)
Other Authors: Susumu Tonegawa.
Format: Thesis
Language:eng
Published: Massachusetts Institute of Technology 2011
Subjects:
Online Access:http://hdl.handle.net/1721.1/62699
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author Murphy, Alexander J. (Alexander James)
author2 Susumu Tonegawa.
author_facet Susumu Tonegawa.
Murphy, Alexander J. (Alexander James)
author_sort Murphy, Alexander J. (Alexander James)
collection MIT
description Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Nuclear Science and Engineering, 2010.
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spelling mit-1721.1/626992019-04-12T12:48:34Z Effect of chemically induced mGluR-dependent long-term depression on dendritic spine volume Murphy, Alexander J. (Alexander James) Susumu Tonegawa. Massachusetts Institute of Technology. Dept. of Nuclear Science and Engineering. Massachusetts Institute of Technology. Dept. of Nuclear Science and Engineering. Nuclear Science and Engineering. 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. 2011-05-09T15:21:59Z 2011-05-09T15:21:59Z 2010 2010 Thesis http://hdl.handle.net/1721.1/62699 714584858 eng 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 36 p. application/pdf Massachusetts Institute of Technology
spellingShingle Nuclear Science and Engineering.
Murphy, Alexander J. (Alexander James)
Effect of chemically induced mGluR-dependent long-term depression on dendritic spine volume
title Effect of chemically induced mGluR-dependent long-term depression on dendritic spine volume
title_full Effect of chemically induced mGluR-dependent long-term depression on dendritic spine volume
title_fullStr Effect of chemically induced mGluR-dependent long-term depression on dendritic spine volume
title_full_unstemmed Effect of chemically induced mGluR-dependent long-term depression on dendritic spine volume
title_short Effect of chemically induced mGluR-dependent long-term depression on dendritic spine volume
title_sort effect of chemically induced mglur dependent long term depression on dendritic spine volume
topic Nuclear Science and Engineering.
url http://hdl.handle.net/1721.1/62699
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