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      Delayed neurogenesis leads to altered specification of ventrotemporal retinal ganglion cells in albino mice

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          Abstract

          Background

          Proper binocular vision depends on the routing at the optic chiasm of the correct proportion of retinal ganglion cell (RGC) axons that project to the same (ipsilateral) and opposite (contralateral) side of the brain. The ipsilateral RGC projection is reduced in mammals with albinism, a congenital disorder characterized by deficient pigmentation in the skin, hair, and eyes. Compared to the pigmented embryonic mouse retina, the albino embryonic mouse retina has fewer RGCs that express the zinc-finger transcription factor, Zic2, which is transiently expressed by RGCs fated to project ipsilaterally. Here, using Zic2 as a marker of ipsilateral RGCs, Islet2 as a marker of contralateral RGCs, and birthdating, we investigate spatiotemporal dynamics of RGC production as they relate to the phenotype of diminished ipsilateral RGC number in the albino retina.

          Results

          At embryonic day (E)15.5, fewer Zic2-positive (Zic2 +) RGCs are found in the albino ventrotemporal (VT) retina compared with the pigmented VT retina, as we previously reported. However, the reduction in Zic2 + RGCs in the albino is not accompanied by a compensatory increase in Zic2-negative (Zic2 ) RGCs, resulting in fewer RGCs in the VT retina at this time point. At E17.5, however, the number of RGCs in the VT region is similar in pigmented and albino retinae, implicating a shift in the timing of RGC production in the albino. Short-term birthdating assays reveal a delay in RGC production in the albino VT retina between E13 and E15. Specifically, fewer Zic2 + RGCs are born at E13 and more Zic2 RGCs are born at E15. Consistent with an increase in the production of Zic2 RGCs born at later ages, more RGCs at E17.5 express the contralateral marker, Islet2, in the albino VT retina compared with the pigmented retina.

          Conclusions

          A delay in neurogenesis in the albino retina is linked to the alteration of RGC subtype specification and consequently leads to the reduced ipsilateral projection that characterizes albinism.

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          Most cited references53

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          A chemical method for fast and sensitive detection of DNA synthesis in vivo.

          We have developed a method to detect DNA synthesis in proliferating cells, based on the incorporation of 5-ethynyl-2'-deoxyuridine (EdU) and its subsequent detection by a fluorescent azide through a Cu(I)-catalyzed [3 + 2] cycloaddition reaction ("click" chemistry). Detection of the EdU label is highly sensitive and can be accomplished in minutes. The small size of the fluorescent azides used for detection results in a high degree of specimen penetration, allowing the staining of whole-mount preparations of large tissue and organ explants. In contrast to BrdU, the method does not require sample fixation or DNA denaturation and permits good structural preservation. We demonstrate the use of the method in cultured cells and in the intestine and brain of whole animals.
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            Cell fate determination in the vertebrate retina.

            The vertebrate retina is a well-characterized and tractable model for studying neurogenesis. Retinal neurons and glia are generated in a conserved sequence from a pool of multipotent progenitor cells, and numerous cell fate determinants for the different classes of retinal cell types have been identified. Here, we summarize several recent developments in the field that have advanced understanding of the regulation of multipotentiality and temporal competence of progenitors. We also discuss recent insights into the relative influence of lineage-based versus stochastic modes of cell fate determination. Enhancing and integrating knowledge of the molecular and genetic machinery underlying retinal development is critically important for understanding not only normal developmental mechanisms, but also therapeutic interventions aimed at restoring vision loss. Crown Copyright © 2012. Published by Elsevier Ltd. All rights reserved.
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              Decision by division: making cortical maps.

              In the past three decades, mounting evidence has revealed that specification of the basic cortical neuronal classes starts at the time of their final mitotic divisions in the embryonic proliferative zones. This early cell determination continues during the migration of the newborn neurons across the widening cerebral wall, and it is in the cortical plate that they attain their final positions and establish species-specific cytoarchitectonic areas. Here, the development and evolutionary expansion of the neocortex is viewed in the context of the radial unit and protomap hypotheses. A broad spectrum of findings gave insight into the pathogenesis of cortical malformations and the biological bases for the evolution of the modern human neocortex. We examine the history and evidence behind the concept of early specification of neurons and provide the latest compendium of genes and signaling molecules involved in neuronal fate determination and specification.
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                Author and article information

                Contributors
                Journal
                Neural Dev
                Neural Dev
                Neural Development
                BioMed Central
                1749-8104
                2014
                18 May 2014
                : 9
                : 11
                Affiliations
                [1 ]Department of Pathology and Cell Biology, College of Physicians and Surgeons, Columbia University, New York, USA
                [2 ]Department of Neuroscience, College of Physicians and Surgeons, Columbia University, New York, USA
                [3 ]Department of Ophthalmology, College of Physicians and Surgeons, Columbia University, New York, USA
                [4 ]Current address: Department of Ophthalmology, Albert Einstein College of Medicine, New York, USA
                [5 ]Current address: INSERM UMR-S839, Institut du Fer à Moulin, Paris, France
                Article
                1749-8104-9-11
                10.1186/1749-8104-9-11
                4072486
                24885435
                3730f88b-380e-4771-9661-451ba656085b
                Copyright © 2014 Bhansali et al.; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 8 March 2014
                : 29 April 2014
                Categories
                Research Article

                Neurosciences
                retinal ganglion cell,albino,neurogenesis,cell specification,zic2,ipsilateral,contralateral,binocular visual pathway

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