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AMIGO2 Scales Dendrite Arbors in the Retina
The size of dendrite arbors shapes their function and differs vastly between neuron types. The signals that control dendritic arbor size remain obscure. Here, we find that in the retina, starburst amacrine cells (SACs) and rod bipolar cells (RBCs) express the homophilic cell-surface protein AMIGO2....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6871773/ https://www.ncbi.nlm.nih.gov/pubmed/31693896 http://dx.doi.org/10.1016/j.celrep.2019.09.085 |
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author | Soto, Florentina Tien, Nai-Wen Goel, Anurag Zhao, Lei Ruzycki, Philip A. Kerschensteiner, Daniel |
author_facet | Soto, Florentina Tien, Nai-Wen Goel, Anurag Zhao, Lei Ruzycki, Philip A. Kerschensteiner, Daniel |
author_sort | Soto, Florentina |
collection | PubMed |
description | The size of dendrite arbors shapes their function and differs vastly between neuron types. The signals that control dendritic arbor size remain obscure. Here, we find that in the retina, starburst amacrine cells (SACs) and rod bipolar cells (RBCs) express the homophilic cell-surface protein AMIGO2. In Amigo2 knockout (KO) mice, SAC and RBC dendrites expand while arbors of other retinal neurons remain stable. SAC dendrites are divided into a central input region and a peripheral output region that provides asymmetric inhibition to direction-selective ganglion cells (DSGCs). Input and output compartments scale precisely with increased arbor size in Amigo2 KO mice, and SAC dendrites maintain asymmetric connectivity with DSGCs. Increased coverage of SAC dendrites is accompanied by increased direction selectivity of DSGCs without changes to other ganglion cells. Our results identify AMIGO2 as a cell-type-specific dendritic scaling factor and link dendrite size and coverage to visual feature detection. |
format | Online Article Text |
id | pubmed-6871773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-68717732019-11-21 AMIGO2 Scales Dendrite Arbors in the Retina Soto, Florentina Tien, Nai-Wen Goel, Anurag Zhao, Lei Ruzycki, Philip A. Kerschensteiner, Daniel Cell Rep Article The size of dendrite arbors shapes their function and differs vastly between neuron types. The signals that control dendritic arbor size remain obscure. Here, we find that in the retina, starburst amacrine cells (SACs) and rod bipolar cells (RBCs) express the homophilic cell-surface protein AMIGO2. In Amigo2 knockout (KO) mice, SAC and RBC dendrites expand while arbors of other retinal neurons remain stable. SAC dendrites are divided into a central input region and a peripheral output region that provides asymmetric inhibition to direction-selective ganglion cells (DSGCs). Input and output compartments scale precisely with increased arbor size in Amigo2 KO mice, and SAC dendrites maintain asymmetric connectivity with DSGCs. Increased coverage of SAC dendrites is accompanied by increased direction selectivity of DSGCs without changes to other ganglion cells. Our results identify AMIGO2 as a cell-type-specific dendritic scaling factor and link dendrite size and coverage to visual feature detection. 2019-11-05 /pmc/articles/PMC6871773/ /pubmed/31693896 http://dx.doi.org/10.1016/j.celrep.2019.09.085 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 Soto, Florentina Tien, Nai-Wen Goel, Anurag Zhao, Lei Ruzycki, Philip A. Kerschensteiner, Daniel AMIGO2 Scales Dendrite Arbors in the Retina |
title | AMIGO2 Scales Dendrite Arbors in the Retina |
title_full | AMIGO2 Scales Dendrite Arbors in the Retina |
title_fullStr | AMIGO2 Scales Dendrite Arbors in the Retina |
title_full_unstemmed | AMIGO2 Scales Dendrite Arbors in the Retina |
title_short | AMIGO2 Scales Dendrite Arbors in the Retina |
title_sort | amigo2 scales dendrite arbors in the retina |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6871773/ https://www.ncbi.nlm.nih.gov/pubmed/31693896 http://dx.doi.org/10.1016/j.celrep.2019.09.085 |
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