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Cell-Type Specific Roles for PTEN in Establishing a Functional Retinal Architecture

BACKGROUND: The retina has a unique three-dimensional architecture, the precise organization of which allows for complete sampling of the visual field. Along the radial or apicobasal axis, retinal neurons and their dendritic and axonal arbors are segregated into layers, while perpendicular to this a...

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Autores principales: Cantrup, Robert, Dixit, Rajiv, Palmesino, Elena, Bonfield, Stephan, Shaker, Tarek, Tachibana, Nobuhiko, Zinyk, Dawn, Dalesman, Sarah, Yamakawa, Kazuhiro, Stell, William K., Wong, Rachel O., Reese, Benjamin E., Kania, Artur, Sauvé, Yves, Schuurmans, Carol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293905/
https://www.ncbi.nlm.nih.gov/pubmed/22403711
http://dx.doi.org/10.1371/journal.pone.0032795
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author Cantrup, Robert
Dixit, Rajiv
Palmesino, Elena
Bonfield, Stephan
Shaker, Tarek
Tachibana, Nobuhiko
Zinyk, Dawn
Dalesman, Sarah
Yamakawa, Kazuhiro
Stell, William K.
Wong, Rachel O.
Reese, Benjamin E.
Kania, Artur
Sauvé, Yves
Schuurmans, Carol
author_facet Cantrup, Robert
Dixit, Rajiv
Palmesino, Elena
Bonfield, Stephan
Shaker, Tarek
Tachibana, Nobuhiko
Zinyk, Dawn
Dalesman, Sarah
Yamakawa, Kazuhiro
Stell, William K.
Wong, Rachel O.
Reese, Benjamin E.
Kania, Artur
Sauvé, Yves
Schuurmans, Carol
author_sort Cantrup, Robert
collection PubMed
description BACKGROUND: The retina has a unique three-dimensional architecture, the precise organization of which allows for complete sampling of the visual field. Along the radial or apicobasal axis, retinal neurons and their dendritic and axonal arbors are segregated into layers, while perpendicular to this axis, in the tangential plane, four of the six neuronal types form patterned cellular arrays, or mosaics. Currently, the molecular cues that control retinal cell positioning are not well-understood, especially those that operate in the tangential plane. Here we investigated the role of the PTEN phosphatase in establishing a functional retinal architecture. METHODOLOGY/PRINCIPAL FINDINGS: In the developing retina, PTEN was localized preferentially to ganglion, amacrine and horizontal cells, whose somata are distributed in mosaic patterns in the tangential plane. Generation of a retina-specific Pten knock-out resulted in retinal ganglion, amacrine and horizontal cell hypertrophy, and expansion of the inner plexiform layer. The spacing of Pten mutant mosaic populations was also aberrant, as were the arborization and fasciculation patterns of their processes, displaying cell type-specific defects in the radial and tangential dimensions. Irregular oscillatory potentials were also observed in Pten mutant electroretinograms, indicative of asynchronous amacrine cell firing. Furthermore, while Pten mutant RGC axons targeted appropriate brain regions, optokinetic spatial acuity was reduced in Pten mutant animals. Finally, while some features of the Pten mutant retina appeared similar to those reported in Dscam-mutant mice, PTEN expression and activity were normal in the absence of Dscam. CONCLUSIONS/SIGNIFICANCE: We conclude that Pten regulates somal positioning and neurite arborization patterns of a subset of retinal cells that form mosaics, likely functioning independently of Dscam, at least during the embryonic period. Our findings thus reveal an unexpected level of cellular specificity for the multi-purpose phosphatase, and identify Pten as an integral component of a novel cell positioning pathway in the retina.
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spelling pubmed-32939052012-03-08 Cell-Type Specific Roles for PTEN in Establishing a Functional Retinal Architecture Cantrup, Robert Dixit, Rajiv Palmesino, Elena Bonfield, Stephan Shaker, Tarek Tachibana, Nobuhiko Zinyk, Dawn Dalesman, Sarah Yamakawa, Kazuhiro Stell, William K. Wong, Rachel O. Reese, Benjamin E. Kania, Artur Sauvé, Yves Schuurmans, Carol PLoS One Research Article BACKGROUND: The retina has a unique three-dimensional architecture, the precise organization of which allows for complete sampling of the visual field. Along the radial or apicobasal axis, retinal neurons and their dendritic and axonal arbors are segregated into layers, while perpendicular to this axis, in the tangential plane, four of the six neuronal types form patterned cellular arrays, or mosaics. Currently, the molecular cues that control retinal cell positioning are not well-understood, especially those that operate in the tangential plane. Here we investigated the role of the PTEN phosphatase in establishing a functional retinal architecture. METHODOLOGY/PRINCIPAL FINDINGS: In the developing retina, PTEN was localized preferentially to ganglion, amacrine and horizontal cells, whose somata are distributed in mosaic patterns in the tangential plane. Generation of a retina-specific Pten knock-out resulted in retinal ganglion, amacrine and horizontal cell hypertrophy, and expansion of the inner plexiform layer. The spacing of Pten mutant mosaic populations was also aberrant, as were the arborization and fasciculation patterns of their processes, displaying cell type-specific defects in the radial and tangential dimensions. Irregular oscillatory potentials were also observed in Pten mutant electroretinograms, indicative of asynchronous amacrine cell firing. Furthermore, while Pten mutant RGC axons targeted appropriate brain regions, optokinetic spatial acuity was reduced in Pten mutant animals. Finally, while some features of the Pten mutant retina appeared similar to those reported in Dscam-mutant mice, PTEN expression and activity were normal in the absence of Dscam. CONCLUSIONS/SIGNIFICANCE: We conclude that Pten regulates somal positioning and neurite arborization patterns of a subset of retinal cells that form mosaics, likely functioning independently of Dscam, at least during the embryonic period. Our findings thus reveal an unexpected level of cellular specificity for the multi-purpose phosphatase, and identify Pten as an integral component of a novel cell positioning pathway in the retina. Public Library of Science 2012-03-05 /pmc/articles/PMC3293905/ /pubmed/22403711 http://dx.doi.org/10.1371/journal.pone.0032795 Text en Cantrup et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cantrup, Robert
Dixit, Rajiv
Palmesino, Elena
Bonfield, Stephan
Shaker, Tarek
Tachibana, Nobuhiko
Zinyk, Dawn
Dalesman, Sarah
Yamakawa, Kazuhiro
Stell, William K.
Wong, Rachel O.
Reese, Benjamin E.
Kania, Artur
Sauvé, Yves
Schuurmans, Carol
Cell-Type Specific Roles for PTEN in Establishing a Functional Retinal Architecture
title Cell-Type Specific Roles for PTEN in Establishing a Functional Retinal Architecture
title_full Cell-Type Specific Roles for PTEN in Establishing a Functional Retinal Architecture
title_fullStr Cell-Type Specific Roles for PTEN in Establishing a Functional Retinal Architecture
title_full_unstemmed Cell-Type Specific Roles for PTEN in Establishing a Functional Retinal Architecture
title_short Cell-Type Specific Roles for PTEN in Establishing a Functional Retinal Architecture
title_sort cell-type specific roles for pten in establishing a functional retinal architecture
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293905/
https://www.ncbi.nlm.nih.gov/pubmed/22403711
http://dx.doi.org/10.1371/journal.pone.0032795
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