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Synaptic Convergence Patterns onto Retinal Ganglion Cells Are Preserved despite Topographic Variation in Pre- and Postsynaptic Territories
Sensory processing can be tuned by a neuron’s integration area, the types of inputs, and the proportion and number of connections with those inputs. Integration areas often vary topographically to sample space differentially across regions. Here, we highlight two visual circuits in which topographic...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317877/ https://www.ncbi.nlm.nih.gov/pubmed/30463000 http://dx.doi.org/10.1016/j.celrep.2018.10.089 |
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author | Yu, Wan-Qing El-Danaf, Rana N. Okawa, Haruhisa Pacholec, Justin M. Matti, Ulf Schwarz, Karin Odermatt, Benjamin Dunn, Felice A. Lagnado, Leon Schmitz, Frank Huberman, Andrew D. Wong, Rachel O.L. |
author_facet | Yu, Wan-Qing El-Danaf, Rana N. Okawa, Haruhisa Pacholec, Justin M. Matti, Ulf Schwarz, Karin Odermatt, Benjamin Dunn, Felice A. Lagnado, Leon Schmitz, Frank Huberman, Andrew D. Wong, Rachel O.L. |
author_sort | Yu, Wan-Qing |
collection | PubMed |
description | Sensory processing can be tuned by a neuron’s integration area, the types of inputs, and the proportion and number of connections with those inputs. Integration areas often vary topographically to sample space differentially across regions. Here, we highlight two visual circuits in which topographic changes in the postsynaptic retinal ganglion cell (RGC) dendritic territories and their presynaptic bipolar cell (BC) axonal territories are either matched or unmatched. Despite this difference, in both circuits, the proportion of inputs from each BC type, i.e., synaptic convergence between specific BCs and RGCs, remained constant across varying dendritic territory sizes. Furthermore, synapse density between BCs and RGCs was invariant across topography. Our results demonstrate a wiring design, likely engaging homotypic axonal tiling of BCs, that ensures consistency in synaptic convergence between specific BC types onto their target RGCs while enabling independent regulation of pre- and post-synaptic territory sizes and synapse number between cell pairs. |
format | Online Article Text |
id | pubmed-6317877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-63178772019-01-03 Synaptic Convergence Patterns onto Retinal Ganglion Cells Are Preserved despite Topographic Variation in Pre- and Postsynaptic Territories Yu, Wan-Qing El-Danaf, Rana N. Okawa, Haruhisa Pacholec, Justin M. Matti, Ulf Schwarz, Karin Odermatt, Benjamin Dunn, Felice A. Lagnado, Leon Schmitz, Frank Huberman, Andrew D. Wong, Rachel O.L. Cell Rep Article Sensory processing can be tuned by a neuron’s integration area, the types of inputs, and the proportion and number of connections with those inputs. Integration areas often vary topographically to sample space differentially across regions. Here, we highlight two visual circuits in which topographic changes in the postsynaptic retinal ganglion cell (RGC) dendritic territories and their presynaptic bipolar cell (BC) axonal territories are either matched or unmatched. Despite this difference, in both circuits, the proportion of inputs from each BC type, i.e., synaptic convergence between specific BCs and RGCs, remained constant across varying dendritic territory sizes. Furthermore, synapse density between BCs and RGCs was invariant across topography. Our results demonstrate a wiring design, likely engaging homotypic axonal tiling of BCs, that ensures consistency in synaptic convergence between specific BC types onto their target RGCs while enabling independent regulation of pre- and post-synaptic territory sizes and synapse number between cell pairs. 2018-11-20 /pmc/articles/PMC6317877/ /pubmed/30463000 http://dx.doi.org/10.1016/j.celrep.2018.10.089 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Yu, Wan-Qing El-Danaf, Rana N. Okawa, Haruhisa Pacholec, Justin M. Matti, Ulf Schwarz, Karin Odermatt, Benjamin Dunn, Felice A. Lagnado, Leon Schmitz, Frank Huberman, Andrew D. Wong, Rachel O.L. Synaptic Convergence Patterns onto Retinal Ganglion Cells Are Preserved despite Topographic Variation in Pre- and Postsynaptic Territories |
title | Synaptic Convergence Patterns onto Retinal Ganglion Cells Are Preserved despite Topographic Variation in Pre- and Postsynaptic Territories |
title_full | Synaptic Convergence Patterns onto Retinal Ganglion Cells Are Preserved despite Topographic Variation in Pre- and Postsynaptic Territories |
title_fullStr | Synaptic Convergence Patterns onto Retinal Ganglion Cells Are Preserved despite Topographic Variation in Pre- and Postsynaptic Territories |
title_full_unstemmed | Synaptic Convergence Patterns onto Retinal Ganglion Cells Are Preserved despite Topographic Variation in Pre- and Postsynaptic Territories |
title_short | Synaptic Convergence Patterns onto Retinal Ganglion Cells Are Preserved despite Topographic Variation in Pre- and Postsynaptic Territories |
title_sort | synaptic convergence patterns onto retinal ganglion cells are preserved despite topographic variation in pre- and postsynaptic territories |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317877/ https://www.ncbi.nlm.nih.gov/pubmed/30463000 http://dx.doi.org/10.1016/j.celrep.2018.10.089 |
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