Impaired and enhanced spatial representation of the PSD-95 knockout mouse

Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, June 2004.

Bibliographic Details
Main Author: Sun, Linus Da-Shih, 1972-
Other Authors: Matthew A. Wilson.
Format: Thesis
Language:en_US
Published: Massachusetts Institute of Technology 2005
Subjects:
Online Access:http://hdl.handle.net/1721.1/27046
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author Sun, Linus Da-Shih, 1972-
author2 Matthew A. Wilson.
author_facet Matthew A. Wilson.
Sun, Linus Da-Shih, 1972-
author_sort Sun, Linus Da-Shih, 1972-
collection MIT
description Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, June 2004.
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spelling mit-1721.1/270462019-04-12T09:44:55Z Impaired and enhanced spatial representation of the PSD-95 knockout mouse Sun, Linus Da-Shih, 1972- Matthew A. Wilson. Massachusetts Institute of Technology. Dept. of Biology. Massachusetts Institute of Technology. Dept. of Biology. Biology. Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, June 2004. Includes bibliographical references (p. 175-185). Postsynaptic density protein-95 (PSD-95) is the second most abundantly expressed synaptic protein in the postnatal forebrain. It is an integral part of the postsynaptic scaffolding complex and helps recruit receptors, channels and associated factors involved with synaptic transmission. A mouse whose wildtype gene was replaced with truncation mutant of PSD-95 preserving two PDZ binding domains causes a spatial learning and memory deficit and a dramatic enhancement of synaptic strengthening. Long Term Potentiation is enhanced at all frequencies of stimulation (1-100Hz), while Long Term Depression is absent in the mutants. This study explores CA1 pyramidal cell spatial representations in the PSD-95 mutant mice. Mutants are not significantly different than controls in running velocity. Nor are its pyramidal cells or interneurons different than controls in: place cell firing rates, sparsity of run active cells, bursting behavior, or theta modulated activity. However, mutants do exhibit significantly larger place fields and wider spike waveforms. Mutants also expressed enhanced directionality of place fields and increased post-run sleep correlation of firing for overlapping place fields. Mutants also exhibited disruption of asymmetrical place fields and phase precession, the first such observation reported in mice. In conclusion, LTP alone is not enough for the active process of encoding experience. Instead, bi-directional synaptic plasticity is necessary for proper place field formation, correlation, directionality, asymmetry, phase precession, and the formation of spatial memories. by Linus Da-Shih Sun. Ph.D. 2005-09-06T21:28:01Z 2005-09-06T21:28:01Z 2003 2004 Thesis http://hdl.handle.net/1721.1/27046 56795379 en_US 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 185, [593]-604 p. 15640481 bytes 15668795 bytes application/pdf application/pdf application/pdf Massachusetts Institute of Technology
spellingShingle Biology.
Sun, Linus Da-Shih, 1972-
Impaired and enhanced spatial representation of the PSD-95 knockout mouse
title Impaired and enhanced spatial representation of the PSD-95 knockout mouse
title_full Impaired and enhanced spatial representation of the PSD-95 knockout mouse
title_fullStr Impaired and enhanced spatial representation of the PSD-95 knockout mouse
title_full_unstemmed Impaired and enhanced spatial representation of the PSD-95 knockout mouse
title_short Impaired and enhanced spatial representation of the PSD-95 knockout mouse
title_sort impaired and enhanced spatial representation of the psd 95 knockout mouse
topic Biology.
url http://hdl.handle.net/1721.1/27046
work_keys_str_mv AT sunlinusdashih1972 impairedandenhancedspatialrepresentationofthepsd95knockoutmouse