A connectomic analysis of the directional selectivity circuit in the mouse retina

Thesis: Ph. D., Massachusetts Institute of Technology, Department of Brain and Cognitive Sciences, June 2016. === Cataloged from PDF version of thesis. === Includes bibliographical references (pages 51-56). === This thesis addresses the question of how direction selectivity (DS) arises in the mouse...

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Main Author: Greene, Matthew (Matthew Jason)
Other Authors: H. Sebastian Seung.
Format: Others
Language:English
Published: Massachusetts Institute of Technology 2017
Subjects:
Online Access:http://hdl.handle.net/1721.1/106432
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spelling ndltd-MIT-oai-dspace.mit.edu-1721.1-1064322019-05-02T15:45:15Z A connectomic analysis of the directional selectivity circuit in the mouse retina Greene, Matthew (Matthew Jason) H. Sebastian Seung. Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences. Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences. Brain and Cognitive Sciences. Thesis: Ph. D., Massachusetts Institute of Technology, Department of Brain and Cognitive Sciences, June 2016. Cataloged from PDF version of thesis. Includes bibliographical references (pages 51-56). This thesis addresses the question of how direction selectivity (DS) arises in the mouse retina. DS has long been observed in retinal ganglion cells, and more recently confirmed in the starburst amacrine cell. Upstream retinal bipolar cells, however, have been shown to lac, indicating that the mechanism that gives rise to DS lies in the inner plexiform layer, where the axons of bipolar cells costratify with amacrine and ganglion cells. We reconstructed a region of the IPL and identified cell types within it, and have discovered a mechanism which may explain the origin of DS activity in the mammalian retina, which relies on what we call "space-time wiring specificity." It has been suggested that a DS signal can arise from non-DS excitatory inputs if at least one among spatially segregated inputs transmits its signal with some delay, which we extend to consider also a difference in the degree to which the signal is sustained. Previously, it has been supposed that this delay occurs within the starburst amacrine cells' dendrites. We hypothesized an alternative, presynaptic mechanism. We observed that different bipolar cell types, which are believed to express different degrees of sustained activity, contact different regions of the starburst amacrine cell dendrite, giving rise to a space-time wiring specifity that should produce a DS signal. We additionally provide a model that predicts the strength of DS as a function of the spatial segregation of inputs and the temporal delay. by Matthew Greene. Ph. D. 2017-01-12T18:33:15Z 2017-01-12T18:33:15Z 2014 2016 Thesis http://hdl.handle.net/1721.1/106432 967336369 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 56 pages application/pdf Massachusetts Institute of Technology
collection NDLTD
language English
format Others
sources NDLTD
topic Brain and Cognitive Sciences.
spellingShingle Brain and Cognitive Sciences.
Greene, Matthew (Matthew Jason)
A connectomic analysis of the directional selectivity circuit in the mouse retina
description Thesis: Ph. D., Massachusetts Institute of Technology, Department of Brain and Cognitive Sciences, June 2016. === Cataloged from PDF version of thesis. === Includes bibliographical references (pages 51-56). === This thesis addresses the question of how direction selectivity (DS) arises in the mouse retina. DS has long been observed in retinal ganglion cells, and more recently confirmed in the starburst amacrine cell. Upstream retinal bipolar cells, however, have been shown to lac, indicating that the mechanism that gives rise to DS lies in the inner plexiform layer, where the axons of bipolar cells costratify with amacrine and ganglion cells. We reconstructed a region of the IPL and identified cell types within it, and have discovered a mechanism which may explain the origin of DS activity in the mammalian retina, which relies on what we call "space-time wiring specificity." It has been suggested that a DS signal can arise from non-DS excitatory inputs if at least one among spatially segregated inputs transmits its signal with some delay, which we extend to consider also a difference in the degree to which the signal is sustained. Previously, it has been supposed that this delay occurs within the starburst amacrine cells' dendrites. We hypothesized an alternative, presynaptic mechanism. We observed that different bipolar cell types, which are believed to express different degrees of sustained activity, contact different regions of the starburst amacrine cell dendrite, giving rise to a space-time wiring specifity that should produce a DS signal. We additionally provide a model that predicts the strength of DS as a function of the spatial segregation of inputs and the temporal delay. === by Matthew Greene. === Ph. D.
author2 H. Sebastian Seung.
author_facet H. Sebastian Seung.
Greene, Matthew (Matthew Jason)
author Greene, Matthew (Matthew Jason)
author_sort Greene, Matthew (Matthew Jason)
title A connectomic analysis of the directional selectivity circuit in the mouse retina
title_short A connectomic analysis of the directional selectivity circuit in the mouse retina
title_full A connectomic analysis of the directional selectivity circuit in the mouse retina
title_fullStr A connectomic analysis of the directional selectivity circuit in the mouse retina
title_full_unstemmed A connectomic analysis of the directional selectivity circuit in the mouse retina
title_sort connectomic analysis of the directional selectivity circuit in the mouse retina
publisher Massachusetts Institute of Technology
publishDate 2017
url http://hdl.handle.net/1721.1/106432
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