Analysis of neural circuits in vitro

Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Brain and Cognitive Sciences, 2010.

Bibliographic Details
Main Author: Wang, Jennifer Lynn
Other Authors: H. Sebastian Seung.
Format: Thesis
Language:eng
Published: Massachusetts Institute of Technology 2011
Subjects:
Online Access:http://hdl.handle.net/1721.1/61878
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author Wang, Jennifer Lynn
author2 H. Sebastian Seung.
author_facet H. Sebastian Seung.
Wang, Jennifer Lynn
author_sort Wang, Jennifer Lynn
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description Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Brain and Cognitive Sciences, 2010.
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spelling mit-1721.1/618782019-04-10T07:13:21Z Analysis of neural circuits in vitro Wang, Jennifer Lynn H. Sebastian Seung. Massachusetts Institute of Technology. Dept. of Brain and Cognitive Sciences. Massachusetts Institute of Technology. Dept. of Brain and Cognitive Sciences. Brain and Cognitive Sciences. Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Brain and Cognitive Sciences, 2010. Cataloged from PDF version of thesis. Includes bibliographical references. This thesis is a collection of manuscripts addressing connectivity of neural circuits in cultured hippocampal neurons. These studies begin with an investigation of dopaminergic modulation of excitatory synapses in small circuits of neurons grown on glial micro islands. We found that dopamine transiently depressed excitatory synaptic transmission. Scaling up to larger circuits of neurons proved more challenging, since finding connected pairs became combinatorially more improbable. The discovery and use of light-activatable ion channel channel rhodopsin-2 (ChR2) promised to revolutionize the way in which we could map connectivity in vitro. We successfully delivered the gene for ChR2 in hippocampal cultures using recombinant adeno-associated virus and characterized the spatial resolution, as well as the reliability of stimulating action potentials. However, there were limitations to this technique that would render circuit maps ambiguous and incomplete. More recently, the engineering of rabies virus (RV) as a neural circuit tracer has produced an exciting method whereby viral infection can be targeted to a population of neurons and spread of the virus restricted to monosynaptically connected neurons. We further investigated potential mechanisms for previous observations which claim that RV spread is restricted to synaptically connected neurons by manipulating neural activity and synaptic vesicle release. We found that RV spread increased for blockade of synaptic vesicle exocytosis and for blockade of neural activity. The underlying premise for pursuing these methods to elucidate connectivity is that the computational power of the brain comes from changeable, malleable connectivity and that to test network models of computation in a biological brain, we must map the connectivity between individual neurons. This thesis builds a framework for experiments designed to bridge the gap between computational learning theories and networks of live neurons. by Jennifer Lynn Wang. Ph.D. 2011-03-24T20:20:26Z 2011-03-24T20:20:26Z 2010 2010 Thesis http://hdl.handle.net/1721.1/61878 706131930 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 61 p. application/pdf Massachusetts Institute of Technology
spellingShingle Brain and Cognitive Sciences.
Wang, Jennifer Lynn
Analysis of neural circuits in vitro
title Analysis of neural circuits in vitro
title_full Analysis of neural circuits in vitro
title_fullStr Analysis of neural circuits in vitro
title_full_unstemmed Analysis of neural circuits in vitro
title_short Analysis of neural circuits in vitro
title_sort analysis of neural circuits in vitro
topic Brain and Cognitive Sciences.
url http://hdl.handle.net/1721.1/61878
work_keys_str_mv AT wangjenniferlynn analysisofneuralcircuitsinvitro