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      Loss of Function of the Neural Cell Adhesion Molecule NrCAM Regulates Differentiation, Proliferation and Neurogenesis in Early Postnatal Hypothalamic Tanycytes

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          Abstract

          Hypothalamic tanycytes are neural stem and progenitor cells, but little is known of how they are regulated. Here we provide evidence that the cell adhesion molecule, NrCAM, regulates tanycytes in the adult niche. NrCAM is strongly expressed in adult mouse tanycytes. Immunohistochemical and in situ hybridization analysis revealed that NrCAM loss of function leads to both a reduced number of tanycytes and reduced expression of tanycyte-specific cell markers, along with a small reduction in tyrosine hydroxylase-positive arcuate neurons. Similar analyses of NrCAM mutants at E16 identify few changes in gene expression or cell composition, indicating that NrCAM regulates tanycytes, rather than early embryonic hypothalamic development. Neurosphere and organotypic assays support the idea that NrCAM governs cellular homeostasis. Single-cell RNA sequencing (scRNA-Seq) shows that tanycyte-specific genes, including a number that are implicated in thyroid hormone metabolism, show reduced expression in the mutant mouse. However, the mild tanycyte depletion and loss of markers observed in NrCAM-deficient mice were associated with only a subtle metabolic phenotype.

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          Genome-wide atlas of gene expression in the adult mouse brain.

          Molecular approaches to understanding the functional circuitry of the nervous system promise new insights into the relationship between genes, brain and behaviour. The cellular diversity of the brain necessitates a cellular resolution approach towards understanding the functional genomics of the nervous system. We describe here an anatomically comprehensive digital atlas containing the expression patterns of approximately 20,000 genes in the adult mouse brain. Data were generated using automated high-throughput procedures for in situ hybridization and data acquisition, and are publicly accessible online. Newly developed image-based informatics tools allow global genome-scale structural analysis and cross-correlation, as well as identification of regionally enriched genes. Unbiased fine-resolution analysis has identified highly specific cellular markers as well as extensive evidence of cellular heterogeneity not evident in classical neuroanatomical atlases. This highly standardized atlas provides an open, primary data resource for a wide variety of further studies concerning brain organization and function.
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            Neurons derived from radial glial cells establish radial units in neocortex.

            The neocortex of the adult brain consists of neurons and glia that are generated by precursor cells of the embryonic ventricular zone. In general, glia are generated after neurons during development, but radial glia are an exception to this rule. Radial glia are generated before neurogenesis and guide neuronal migration. Radial glia are mitotically active throughout neurogenesis, and disappear or become astrocytes when neuronal migration is complete. Although the lineage relationships of cortical neurons and glia have been explored, the clonal relationship of radial glia to other cortical cells remains unknown. It has been suggested that radial glia may be neuronal precursors, but this has not been demonstrated in vivo. We have used a retroviral vector encoding enhanced green fluorescent protein to label precursor cells in vivo and have examined clones 1-3 days later using morphological, immunohistochemical and electrophysiological techniques. Here we show that clones consist of mitotic radial glia and postmitotic neurons, and that neurons migrate along clonally related radial glia. Time-lapse images show that proliferative radial glia generate neurons. Our results support the concept that a lineage relationship between neurons and proliferative radial glia may underlie the radial organization of neocortex.
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              Integrins: bidirectional, allosteric signaling machines.

              In their roles as major adhesion receptors, integrins signal across the plasma membrane in both directions. Recent structural and cell biological data suggest models for how integrins transmit signals between their extracellular ligand binding adhesion sites and their cytoplasmic domains, which link to the cytoskeleton and to signal transduction pathways. Long-range conformational changes couple these functions via allosteric equilibria.
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                Author and article information

                Contributors
                Journal
                Front Neurosci
                Front Neurosci
                Front. Neurosci.
                Frontiers in Neuroscience
                Frontiers Media S.A.
                1662-4548
                1662-453X
                07 April 2022
                2022
                : 16
                : 832961
                Affiliations
                [1] 1School of Biosciences, The University of Sheffield , Sheffield, United Kingdom
                [2] 2Bateson Centre, The University of Sheffield , Sheffield, United Kingdom
                [3] 3Neuroscience Institute, The University of Sheffield , Sheffield, United Kingdom
                [4] 4Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine , Baltimore, MD, United States
                [5] 5Wellcome Trust-Medical Research Council Institute of Metabolic Science-Metabolic Research Laboratories, University of Cambridge , Cambridge, United Kingdom
                [6] 6School of Life Sciences, University of Nottingham , Nottingham, United Kingdom
                [7] 7Department of Ophthalmology, Johns Hopkins University School of Medicine , Baltimore, MD, United States
                [8] 8Department of Neurology, Johns Hopkins University School of Medicine , Baltimore, MD, United States
                [9] 9Institute for Cell Engineering, Johns Hopkins University School of Medicine , Baltimore, MD, United States
                [10] 10Kavli Neuroscience Discovery Institute, Johns Hopkins University School of Medicine , Baltimore, MD, United States
                Author notes

                Edited by: Alain Prochiantz, Collège de France, France

                Reviewed by: Carlos Vicario, Spanish National Research Council (CSIC), Spain; Martine Cohen-Salmon, INSERM U1050 Centre Interdisciplinaire de Recherche en Biologie, France

                *Correspondence: Marysia Placzek, m.placzek@ 123456sheffield.ac.uk

                These authors have contributed equally to this work

                Present addresses: Charlotte Muir, School of Physiology, University of Bristol, Bristol, United Kingdom; Marco Travaglio, Medical Research Council (MRC) Toxicology Unit, University of Cambridge, Cambridge, United Kingdom

                This article was submitted to Neurodevelopment, a section of the journal Frontiers in Neuroscience

                Article
                10.3389/fnins.2022.832961
                9022636
                35464310
                9c39e239-3e12-4378-a431-99907b0763bc
                Copyright © 2022 Moore, Chinnaiya, Kim, Brown, Stewart, Robins, Dowsett, Muir, Travaglio, Lewis, Ebling, Blackshaw, Furley and Placzek.

                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) and the copyright owner(s) 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.

                History
                : 10 December 2021
                : 27 January 2022
                Page count
                Figures: 8, Tables: 0, Equations: 0, References: 68, Pages: 19, Words: 12394
                Funding
                Funded by: Wellcome Trust, doi 10.13039/100010269;
                Funded by: National Institutes of Health, doi 10.13039/100000002;
                Funded by: National Institutes of Health, doi 10.13039/100000002;
                Funded by: Maryland Stem Cell Research Fund, doi 10.13039/100012443;
                Categories
                Neuroscience
                Original Research

                Neurosciences
                tanycyte,nrcam,neural cell adhesion molecules,scrna seq,radial glia,astrocytes,hypothalamus,neurogenesis

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