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Prox1 Is a Marker for AII Amacrine Cells in the Mouse Retina
The transcription factor Prox1 is expressed in multiple cells in the retina during eye development. This study has focused on neuronal Prox1 expression in the inner nuclear layer (INL) of the adult mouse retina. Prox1 immunostaining was evaluated in vertical retinal sections and whole mount preparat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418924/ https://www.ncbi.nlm.nih.gov/pubmed/28529477 http://dx.doi.org/10.3389/fnana.2017.00039 |
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author | Pérez de Sevilla Müller, Luis Azar, Shaghauyegh S. de los Santos, Janira Brecha, Nicholas C. |
author_facet | Pérez de Sevilla Müller, Luis Azar, Shaghauyegh S. de los Santos, Janira Brecha, Nicholas C. |
author_sort | Pérez de Sevilla Müller, Luis |
collection | PubMed |
description | The transcription factor Prox1 is expressed in multiple cells in the retina during eye development. This study has focused on neuronal Prox1 expression in the inner nuclear layer (INL) of the adult mouse retina. Prox1 immunostaining was evaluated in vertical retinal sections and whole mount preparations using a specific antibody directed to the C-terminus of Prox1. Strong immunostaining was observed in numerous amacrine cell bodies and in all horizontal cell bodies in the proximal and distal INL, respectively. Some bipolar cells were also weakly immunostained. Prox1-immunoreactive amacrine cells expressed glycine, and they formed 35 ± 3% of all glycinergic amacrine cells. Intracellular Neurobiotin injections into AII amacrine cells showed that all gap junction-coupled AII amacrine cells express Prox1, and no other Prox1-immunostained amacrine cells were in the immediate area surrounding the injected AII amacrine cell. Prox1-immunoreactive amacrine cell bodies were distributed across the retina, with their highest density (3887 ± 160 cells/mm(2)) in the central retina, 0.5 mm from the optic nerve head, and their lowest density (3133 ± 350 cells/mm(2)) in the mid-peripheral retina, 2 mm from the optic nerve head. Prox1-immunoreactive amacrine cell bodies comprised ~9.8% of the total amacrine cell population, and they formed a non-random mosaic with a regularity index (RI) of 3.4, similar to AII amacrine cells in the retinas of other mammals. Together, these findings indicate that AII amacrine cells are the predominant and likely only amacrine cell type strongly expressing Prox1 in the adult mouse retina, and establish Prox1 as a marker of AII amacrine cells. |
format | Online Article Text |
id | pubmed-5418924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54189242017-05-19 Prox1 Is a Marker for AII Amacrine Cells in the Mouse Retina Pérez de Sevilla Müller, Luis Azar, Shaghauyegh S. de los Santos, Janira Brecha, Nicholas C. Front Neuroanat Neuroscience The transcription factor Prox1 is expressed in multiple cells in the retina during eye development. This study has focused on neuronal Prox1 expression in the inner nuclear layer (INL) of the adult mouse retina. Prox1 immunostaining was evaluated in vertical retinal sections and whole mount preparations using a specific antibody directed to the C-terminus of Prox1. Strong immunostaining was observed in numerous amacrine cell bodies and in all horizontal cell bodies in the proximal and distal INL, respectively. Some bipolar cells were also weakly immunostained. Prox1-immunoreactive amacrine cells expressed glycine, and they formed 35 ± 3% of all glycinergic amacrine cells. Intracellular Neurobiotin injections into AII amacrine cells showed that all gap junction-coupled AII amacrine cells express Prox1, and no other Prox1-immunostained amacrine cells were in the immediate area surrounding the injected AII amacrine cell. Prox1-immunoreactive amacrine cell bodies were distributed across the retina, with their highest density (3887 ± 160 cells/mm(2)) in the central retina, 0.5 mm from the optic nerve head, and their lowest density (3133 ± 350 cells/mm(2)) in the mid-peripheral retina, 2 mm from the optic nerve head. Prox1-immunoreactive amacrine cell bodies comprised ~9.8% of the total amacrine cell population, and they formed a non-random mosaic with a regularity index (RI) of 3.4, similar to AII amacrine cells in the retinas of other mammals. Together, these findings indicate that AII amacrine cells are the predominant and likely only amacrine cell type strongly expressing Prox1 in the adult mouse retina, and establish Prox1 as a marker of AII amacrine cells. Frontiers Media S.A. 2017-05-05 /pmc/articles/PMC5418924/ /pubmed/28529477 http://dx.doi.org/10.3389/fnana.2017.00039 Text en Copyright © 2017 Pérez de Sevilla Müller, Azar, de los Santos and Brecha. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Pérez de Sevilla Müller, Luis Azar, Shaghauyegh S. de los Santos, Janira Brecha, Nicholas C. Prox1 Is a Marker for AII Amacrine Cells in the Mouse Retina |
title | Prox1 Is a Marker for AII Amacrine Cells in the Mouse Retina |
title_full | Prox1 Is a Marker for AII Amacrine Cells in the Mouse Retina |
title_fullStr | Prox1 Is a Marker for AII Amacrine Cells in the Mouse Retina |
title_full_unstemmed | Prox1 Is a Marker for AII Amacrine Cells in the Mouse Retina |
title_short | Prox1 Is a Marker for AII Amacrine Cells in the Mouse Retina |
title_sort | prox1 is a marker for aii amacrine cells in the mouse retina |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418924/ https://www.ncbi.nlm.nih.gov/pubmed/28529477 http://dx.doi.org/10.3389/fnana.2017.00039 |
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