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Protocadherin-dependent dendritic self-avoidance regulates neural connectivity and circuit function

Dendritic and axonal arbors of many neuronal types exhibit self-avoidance, in which branches repel each other. In some cases, these neurites interact with those of neighboring neurons, a phenomenon called self/non-self discrimination. The functional roles of these processes remain unknown. In this s...

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Detalles Bibliográficos
Autores principales: Kostadinov, Dimitar, Sanes, Joshua R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4548410/
https://www.ncbi.nlm.nih.gov/pubmed/26140686
http://dx.doi.org/10.7554/eLife.08964
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author Kostadinov, Dimitar
Sanes, Joshua R
author_facet Kostadinov, Dimitar
Sanes, Joshua R
author_sort Kostadinov, Dimitar
collection PubMed
description Dendritic and axonal arbors of many neuronal types exhibit self-avoidance, in which branches repel each other. In some cases, these neurites interact with those of neighboring neurons, a phenomenon called self/non-self discrimination. The functional roles of these processes remain unknown. In this study, we used retinal starburst amacrine cells (SACs), critical components of a direction-selective circuit, to address this issue. In SACs, both processes are mediated by the gamma-protocadherins (Pcdhgs), a family of 22 recognition molecules. We manipulated Pcdhg expression in SACs and recorded from them and their targets, direction-selective ganglion cells (DSGCs). SACs form autapses when self-avoidance is disrupted and fail to form connections with other SACs when self/non-self discrimination is perturbed. Pcdhgs are also required to prune connections between closely spaced SACs. These alterations degrade the direction selectivity of DSGCs. Thus, self-avoidance, self/non-self discrimination, and synapse elimination are essential for proper function of a circuit that computes directional motion. DOI: http://dx.doi.org/10.7554/eLife.08964.001
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spelling pubmed-45484102015-08-26 Protocadherin-dependent dendritic self-avoidance regulates neural connectivity and circuit function Kostadinov, Dimitar Sanes, Joshua R eLife Developmental Biology and Stem Cells Dendritic and axonal arbors of many neuronal types exhibit self-avoidance, in which branches repel each other. In some cases, these neurites interact with those of neighboring neurons, a phenomenon called self/non-self discrimination. The functional roles of these processes remain unknown. In this study, we used retinal starburst amacrine cells (SACs), critical components of a direction-selective circuit, to address this issue. In SACs, both processes are mediated by the gamma-protocadherins (Pcdhgs), a family of 22 recognition molecules. We manipulated Pcdhg expression in SACs and recorded from them and their targets, direction-selective ganglion cells (DSGCs). SACs form autapses when self-avoidance is disrupted and fail to form connections with other SACs when self/non-self discrimination is perturbed. Pcdhgs are also required to prune connections between closely spaced SACs. These alterations degrade the direction selectivity of DSGCs. Thus, self-avoidance, self/non-self discrimination, and synapse elimination are essential for proper function of a circuit that computes directional motion. DOI: http://dx.doi.org/10.7554/eLife.08964.001 eLife Sciences Publications, Ltd 2015-07-03 /pmc/articles/PMC4548410/ /pubmed/26140686 http://dx.doi.org/10.7554/eLife.08964 Text en © 2015, Kostadinov and Sanes http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology and Stem Cells
Kostadinov, Dimitar
Sanes, Joshua R
Protocadherin-dependent dendritic self-avoidance regulates neural connectivity and circuit function
title Protocadherin-dependent dendritic self-avoidance regulates neural connectivity and circuit function
title_full Protocadherin-dependent dendritic self-avoidance regulates neural connectivity and circuit function
title_fullStr Protocadherin-dependent dendritic self-avoidance regulates neural connectivity and circuit function
title_full_unstemmed Protocadherin-dependent dendritic self-avoidance regulates neural connectivity and circuit function
title_short Protocadherin-dependent dendritic self-avoidance regulates neural connectivity and circuit function
title_sort protocadherin-dependent dendritic self-avoidance regulates neural connectivity and circuit function
topic Developmental Biology and Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4548410/
https://www.ncbi.nlm.nih.gov/pubmed/26140686
http://dx.doi.org/10.7554/eLife.08964
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