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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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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 |
format | Online Article Text |
id | pubmed-4548410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT kostadinovdimitar protocadherindependentdendriticselfavoidanceregulatesneuralconnectivityandcircuitfunction AT sanesjoshuar protocadherindependentdendriticselfavoidanceregulatesneuralconnectivityandcircuitfunction |