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The mosaic of AII amacrine cell bodies in rat retina is indistinguishable from a random distribution
The vertebrate retina contains a large number of different types of neurons that can be distinguished by their morphological properties. Assuming that no location should be without a contribution from the circuitry and function linked to a specific type of neuron, it is expected that the dendritic t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9107964/ https://www.ncbi.nlm.nih.gov/pubmed/35534787 http://dx.doi.org/10.1017/S0952523822000025 |
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author | Liu, Jian Hao Peter, David Olukoya Faldalen Guttormsen, Maren Sofie Hossain, Md Kaykobad Gerking, Yola Veruki, Margaret Lin Hartveit, Espen |
author_facet | Liu, Jian Hao Peter, David Olukoya Faldalen Guttormsen, Maren Sofie Hossain, Md Kaykobad Gerking, Yola Veruki, Margaret Lin Hartveit, Espen |
author_sort | Liu, Jian Hao |
collection | PubMed |
description | The vertebrate retina contains a large number of different types of neurons that can be distinguished by their morphological properties. Assuming that no location should be without a contribution from the circuitry and function linked to a specific type of neuron, it is expected that the dendritic trees of neurons belonging to a type will cover the retina in a regular manner. Thus, for most types of neurons, the contribution to visual processing is thought to be independent of the exact location of individual neurons across the retina. Here, we have investigated the distribution of AII amacrine cells in rat retina. The AII is a multifunctional amacrine cell found in mammals and involved in synaptic microcircuits that contribute to visual processing under both scotopic and photopic conditions. Previous investigations have suggested that AIIs are regularly distributed, with a nearest-neighbor distance regularity index of ~4. It has been argued, however, that this presumed regularity results from treating somas as points, without taking into account their actual spatial extent which constrains the location of other cells of the same type. When we simulated random distributions of cell bodies with size and density similar to real AIIs, we confirmed that the simulated distributions could not be distinguished from the distributions observed experimentally for AIIs in different regions and eccentricities of the retina. The developmental mechanisms that generate the observed distributions of AIIs remain to be investigated. |
format | Online Article Text |
id | pubmed-9107964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91079642022-05-26 The mosaic of AII amacrine cell bodies in rat retina is indistinguishable from a random distribution Liu, Jian Hao Peter, David Olukoya Faldalen Guttormsen, Maren Sofie Hossain, Md Kaykobad Gerking, Yola Veruki, Margaret Lin Hartveit, Espen Vis Neurosci Research Article The vertebrate retina contains a large number of different types of neurons that can be distinguished by their morphological properties. Assuming that no location should be without a contribution from the circuitry and function linked to a specific type of neuron, it is expected that the dendritic trees of neurons belonging to a type will cover the retina in a regular manner. Thus, for most types of neurons, the contribution to visual processing is thought to be independent of the exact location of individual neurons across the retina. Here, we have investigated the distribution of AII amacrine cells in rat retina. The AII is a multifunctional amacrine cell found in mammals and involved in synaptic microcircuits that contribute to visual processing under both scotopic and photopic conditions. Previous investigations have suggested that AIIs are regularly distributed, with a nearest-neighbor distance regularity index of ~4. It has been argued, however, that this presumed regularity results from treating somas as points, without taking into account their actual spatial extent which constrains the location of other cells of the same type. When we simulated random distributions of cell bodies with size and density similar to real AIIs, we confirmed that the simulated distributions could not be distinguished from the distributions observed experimentally for AIIs in different regions and eccentricities of the retina. The developmental mechanisms that generate the observed distributions of AIIs remain to be investigated. Cambridge University Press 2022-05-10 /pmc/articles/PMC9107964/ /pubmed/35534787 http://dx.doi.org/10.1017/S0952523822000025 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited |
spellingShingle | Research Article Liu, Jian Hao Peter, David Olukoya Faldalen Guttormsen, Maren Sofie Hossain, Md Kaykobad Gerking, Yola Veruki, Margaret Lin Hartveit, Espen The mosaic of AII amacrine cell bodies in rat retina is indistinguishable from a random distribution |
title | The mosaic of AII amacrine cell bodies in rat retina is indistinguishable from a random distribution |
title_full | The mosaic of AII amacrine cell bodies in rat retina is indistinguishable from a random distribution |
title_fullStr | The mosaic of AII amacrine cell bodies in rat retina is indistinguishable from a random distribution |
title_full_unstemmed | The mosaic of AII amacrine cell bodies in rat retina is indistinguishable from a random distribution |
title_short | The mosaic of AII amacrine cell bodies in rat retina is indistinguishable from a random distribution |
title_sort | mosaic of aii amacrine cell bodies in rat retina is indistinguishable from a random distribution |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9107964/ https://www.ncbi.nlm.nih.gov/pubmed/35534787 http://dx.doi.org/10.1017/S0952523822000025 |
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