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      Immunoprecipitation and mass spectrometry identify non-cell autonomous Otx2 homeoprotein in the granular and supragranular layers of mouse visual cortex

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          Abstract

          Plasticity in the visual cerebral cortex is regulated by the internalization of Otx2 homeoprotein into parvalbumin neurons in cortical layers II/III and IV. However the Otx2 locus is not active in these neurons and the protein is imported from external sources, including the choroid plexus. Because Otx1 and Otx2 may have redundant functions, we wanted to verify if part of the staining in parvalbumin neurons corresponds to Otx1 transported from cortical layer V neurons. It is demonstrated here that Otx staining in layer IV cells is maintained in Otx1-null mice. The immunoprecipitation of extracts from finely dissected granular and supragranular cortex (layers I-IV) gave immunoblots with a band corresponding to Otx2 and not Otx1. Moreover, high-resolution mass spectrometry analysis after immunoprecipitation identifies two peptides within the Otx2 homeodomain. One of these peptides is specific for Otx2 and is not found in Otx1. These results unambiguously establish that the staining in parvalbumin neurons revealed with the anti-Otx2 antibodies used in our previous studies identifies non-cell autonomous Otx2.

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          Experience-dependent transfer of Otx2 homeoprotein into the visual cortex activates postnatal plasticity.

          Neural circuits are shaped by experience in early postnatal life. Distinct GABAergic connections within visual cortex determine the timing of the critical period for rewiring ocular dominance to establish visual acuity. We find that maturation of the parvalbumin (PV)-cell network that controls plasticity onset is regulated by a selective re-expression of the embryonic Otx2 homeoprotein. Visual experience promoted the accumulation of non-cell-autonomous Otx2 in PV-cells, and cortical infusion of exogenous Otx2 accelerated both PV-cell development and critical period timing. Conversely, conditional removal of Otx2 from non-PV cells or from the visual pathway abolished plasticity. Thus, the experience-dependent transfer of a homeoprotein may establish the physiological milieu for postnatal plasticity of a neural circuit.
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            Critical period revisited: impact on vision.

            Neural circuits are shaped by experience in early postnatal life. The permanent loss of visual acuity (amblyopia) and anatomical remodeling within primary visual cortex following monocular deprivation is a classic example of critical period development from mouse to man. Recent work in rodents reveals a residual subthreshold potentiation of open eye response throughout life. Resetting excitatory-inhibitory balance or removing molecular 'brakes' on structural plasticity may unmask the potential for recovery of function in adulthood. Novel pharmacological or environmental interventions now hold great therapeutic promise based on a deeper understanding of critical period mechanisms.
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              myProMS, a web server for management and validation of mass spectrometry-based proteomic data.

              Curation and interpretation of protein databank-search results by human experts are key aspects of MS-based proteomic data acquisition. These tasks are often overlooked due to the vast amount of data to inspect. We have developed myProMS, a web server designed to ease search results validation and interpretation by improving data organization, mining and sharing between MS specialists and biologists during MS-based collaborative projects. A demo is accessible at http://bioinfo.curie.fr/myproms.
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                Author and article information

                Journal
                F1000Res
                F1000Res
                F1000Research
                F1000Research
                F1000Research (London, UK )
                2046-1402
                30 July 2014
                2014
                : 3
                : 178
                Affiliations
                [1 ]CIRB, CNRS UMR 7241 / INSERM U1050, College de France, 11 place Marcelin Berthelot, 75231 Paris Cedex 05, France
                [2 ]Institute of Genetics and Biophysics, Via Pietro Castellino 111, 80131 Napoli, Italy
                [3 ]IRCCS Neuromed, 86077 Pozzilli (IS), Italy
                [4 ]Institut Curie, Centre de Recherche, Laboratoire de Spectrométrie de Masse Protéomique, 75248 Paris Cedex 05, France
                [1 ]Centro de Biología Molecular Severo Ochoa, CSIC-UAM, Universidad Autonoma de Madrid, Madrid, Spain
                [1 ]Laboratory of Genetics, Salk Institute for Biological Studies, La Jolla, CA, USA
                Author notes

                NK and AAD carried out experimental work

                DA and AS made Otx1 knockout mice

                DF carried out the mass spectroscopy experimental work

                LD supervised mass spectroscopy and proteomic data analysis

                AP and AAD conceived the ideas of the study, designed protocols, and drafted the manuscript

                All authors read, critically revised, and approved the final manuscript

                Competing interests: No competing interests were disclosed.

                Competing interests: No competing interests were disclosed.

                Competing interests: No competing interests were disclosed.

                Article
                10.5256/f1000research.5197.r5640
                4133762
                f0a621fb-d431-4cd2-abc9-226ded7abbd1
                Copyright: © 2014 Kim N et al.

                This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                Data associated with the article are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication).

                History
                : 29 July 2014
                Funding
                Funded by: Région Ile-de-France
                Funded by: FRM
                Funded by: GRL Program
                Award ID: n°2009-00424
                Funded by: ANR
                Award ID: BRAINEVER n°11-BLAN-069467
                Funded by: ERC
                Award ID: Advanced Grant HOMEOSIGN n°339379
                This work was supported by the Région Ile-de-France, the FRM, GRL Program n°2009-00424, ANR grant BRAINEVER n° 11-BLAN-069467, and ERC Advanced Grant HOMEOSIGN n°339379.
                Categories
                Research Article
                Articles
                Chemical Biology of the Cell
                Neuronal Signalling Mechanisms
                Protein Chemistry & Proteomics

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