Central and Peripheral Retina Arise through Distinct Developmental Paths

In the mature eye, three distinct tissue fates, retina, ciliary body, and iris, arrange with a strict linear organization along the central (back) to peripheral (front) axis. The establishment of this topographical relationship within the optic vesicle is not well understood. We use a targeted vital...

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Main Authors: Venters, Sara J., Mikawa, Takashi, Hyer, Jeanette
Format: Online
Language:English
Published: Public Library of Science 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628928/
id pubmed-3628928
recordtype oai_dc
spelling pubmed-36289282013-04-23 Central and Peripheral Retina Arise through Distinct Developmental Paths Venters, Sara J. Mikawa, Takashi Hyer, Jeanette Research Article In the mature eye, three distinct tissue fates, retina, ciliary body, and iris, arrange with a strict linear organization along the central (back) to peripheral (front) axis. The establishment of this topographical relationship within the optic vesicle is not well understood. We use a targeted vital labeling strategy to test the derivation of mature eye tissues from the optic vesicle of the chick embryo. Fate mapping uncovers two distinct origins of the neural retina. Contrary to expectations, the central neural retina has a discrete origin within the posterior optic vesicle. The peripheral retina derives from the distal optic vesicle, sharing a common origin with more peripheral tissue fates. This study identifies for the first time two distinct retinal sub-domains, central and peripheral, which arise during embryogenesis. Identification of these discrete retinal compartments provides a framework for understanding functional and disease processes throughout retinal tissue. Public Library of Science 2013-04-16 /pmc/articles/PMC3628928/ /pubmed/23613848 http://dx.doi.org/10.1371/journal.pone.0061422 Text en © 2013 Venters 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.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Venters, Sara J.
Mikawa, Takashi
Hyer, Jeanette
spellingShingle Venters, Sara J.
Mikawa, Takashi
Hyer, Jeanette
Central and Peripheral Retina Arise through Distinct Developmental Paths
author_facet Venters, Sara J.
Mikawa, Takashi
Hyer, Jeanette
author_sort Venters, Sara J.
title Central and Peripheral Retina Arise through Distinct Developmental Paths
title_short Central and Peripheral Retina Arise through Distinct Developmental Paths
title_full Central and Peripheral Retina Arise through Distinct Developmental Paths
title_fullStr Central and Peripheral Retina Arise through Distinct Developmental Paths
title_full_unstemmed Central and Peripheral Retina Arise through Distinct Developmental Paths
title_sort central and peripheral retina arise through distinct developmental paths
description In the mature eye, three distinct tissue fates, retina, ciliary body, and iris, arrange with a strict linear organization along the central (back) to peripheral (front) axis. The establishment of this topographical relationship within the optic vesicle is not well understood. We use a targeted vital labeling strategy to test the derivation of mature eye tissues from the optic vesicle of the chick embryo. Fate mapping uncovers two distinct origins of the neural retina. Contrary to expectations, the central neural retina has a discrete origin within the posterior optic vesicle. The peripheral retina derives from the distal optic vesicle, sharing a common origin with more peripheral tissue fates. This study identifies for the first time two distinct retinal sub-domains, central and peripheral, which arise during embryogenesis. Identification of these discrete retinal compartments provides a framework for understanding functional and disease processes throughout retinal tissue.
publisher Public Library of Science
publishDate 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628928/
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