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      Myelination of Neuronal Cell Bodies when Myelin Supply Exceeds Axonal Demand

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          Summary

          The correct targeting of myelin is essential for nervous system formation and function. Oligodendrocytes in the CNS myelinate some axons, but not others, and do not myelinate structures including cell bodies and dendrites [ 1]. Recent studies indicate that extrinsic signals, such as neuronal activity [ 2, 3] and cell adhesion molecules [ 4], can bias myelination toward some axons and away from cell bodies and dendrites, indicating that, in vivo, neuronal and axonal cues regulate myelin targeting. In vitro, however, oligodendrocytes have an intrinsic propensity to myelinate [ 5, 6, 7] and can promiscuously wrap inert synthetic structures resembling neuronal processes [ 8, 9] or cell bodies [ 4]. A current therapeutic goal for the treatment of demyelinating diseases is to greatly promote oligodendrogenesis [ 10, 11, 12, 13]; thus, it is important to test how accurately extrinsic signals regulate the oligodendrocyte’s intrinsic program of myelination in vivo. Here, we test the hypothesis that neurons regulate myelination with sufficient stringency to always ensure correct targeting. Surprisingly, however, we find that myelin targeting in vivo is not very stringent and that mistargeting occurs readily when oligodendrocyte and myelin supply exceed axonal demand. We find that myelin is mistargeted to neuronal cell bodies in zebrafish mutants with fewer axons and independently in drug-treated zebrafish with increased oligodendrogenesis. Additionally, by increasing myelin production of oligodendrocytes in zebrafish and mice, we find that excess myelin is also inappropriately targeted to cell bodies. Our results suggest that balancing oligodendrocyte-intrinsic programs of myelin supply with axonal demand is essential for correct myelin targeting in vivo and highlight potential liabilities of strongly promoting oligodendrogenesis.

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          Highlights

          • Balance between axons and myelin production regulates its targeting in vivo

          • Excess myelin is mistargeted to cell bodies

          • Low, but not zero, level of mistargeting during normal development

          • Potential implications for myelin-promoting therapies

          Abstract

          Almeida et al. find that the balance between axon demand and myelin production in the CNS regulates myelin targeting. In the developing CNS, when normal target axons are reduced, oligodendrocyte number increased, or myelin production per oligodendrocyte increased, myelin is mistargeted to cell bodies, including those of neurons.

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          Most cited references34

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          The Tol2kit: a multisite gateway-based construction kit for Tol2 transposon transgenesis constructs.

          Transgenesis is an important tool for assessing gene function. In zebrafish, transgenesis has suffered from three problems: the labor of building complex expression constructs using conventional subcloning; low transgenesis efficiency, leading to mosaicism in transient transgenics and infrequent germline incorporation; and difficulty in identifying germline integrations unless using a fluorescent marker transgene. The Tol2kit system uses site-specific recombination-based cloning (multisite Gateway technology) to allow quick, modular assembly of [promoter]-[coding sequence]-[3' tag] constructs in a Tol2 transposon backbone. It includes a destination vector with a cmlc2:EGFP (enhanced green fluorescent protein) transgenesis marker and a variety of widely useful entry clones, including hsp70 and beta-actin promoters; cytoplasmic, nuclear, and membrane-localized fluorescent proteins; and internal ribosome entry sequence-driven EGFP cassettes for bicistronic expression. The Tol2kit greatly facilitates zebrafish transgenesis, simplifies the sharing of clones, and enables large-scale projects testing the functions of libraries of regulatory or coding sequences. Copyright 2007 Wiley-Liss, Inc.
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            Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination.

            Myelination of axons by oligodendrocytes enables rapid impulse propagation in the central nervous system. But long-term interactions between axons and their myelin sheaths are poorly understood. Here we show that Cnp1, which encodes 2',3'-cyclic nucleotide phosphodiesterase in oligodendrocytes, is essential for axonal survival but not for myelin assembly. In the absence of glial cyclic nucleotide phosphodiesterase, mice developed axonal swellings and neurodegeneration throughout the brain, leading to hydrocephalus and premature death. But, in contrast to previously studied myelin mutants, the ultrastructure, periodicity and physical stability of myelin were not altered in these mice. Genetically, the chief function of glia in supporting axonal integrity can thus be completely uncoupled from its function in maintaining compact myelin. Oligodendrocyte dysfunction, such as that in multiple sclerosis lesions, may suffice to cause secondary axonal loss.
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              Neuronal activity biases axon selection for myelination in vivo

              An essential feature of vertebrate neural development is ensheathment of axons with myelin, an insulating membrane formed by oligodendrocytes. Not all axons are myelinated, but mechanisms directing myelination of specific axons are unknown. Using zebrafish we show that activity-dependent secretion stabilizes myelin sheath formation on select axons. When VAMP2-dependent exocytosis is silenced in single axons, oligodendrocytes preferentially ensheath neighboring axons. Nascent sheaths formed on silenced axons are shorter in length, but when activity of neighboring axons is also suppressed, inhibition of sheath growth is relieved. Using in vivo time-lapse microscopy, we show that only 25% of oligodendrocyte processes that initiate axon wrapping are stabilized during normal development, and that initiation does not require activity. Instead, oligodendrocyte processes wrapping silenced axons are retracted more frequently. We propose that axon selection for myelination results from excessive and indiscriminate initiation of wrapping followed by refinement that is biased by activity-dependent secretion from axons.
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                Author and article information

                Contributors
                Journal
                Curr Biol
                Curr. Biol
                Current Biology
                Cell Press
                0960-9822
                1879-0445
                23 April 2018
                23 April 2018
                : 28
                : 8
                : 1296-1305.e5
                Affiliations
                [1 ]Centre for Discovery Brain Sciences, University of Edinburgh, 49 Little France Crescent, Edinburgh EH16 4SB, UK
                [2 ]Department of Neurology and Program in Neuroscience, University of California, San Francisco, 675 Nelson Rising Lane, San Francisco, CA 94143, USA
                [3 ]Institute of Neuronal Cell Biology, Technical University of Munich, Biedersteiner Strasse 29, 80802 Munich, Germany
                [4 ]Munich Cluster of Systems Neurology (SyNergy), Feodor-Lynen Strasse 17, 81377 Munich, Germany
                Author notes
                []Corresponding author david.lyons@ 123456ed.ac.uk
                [5]

                Lead Contact

                Article
                S0960-9822(18)30254-9
                10.1016/j.cub.2018.02.068
                5912901
                29628374
                12619add-cecb-4a47-bd5c-2c55701cf171
                © 2018 The Author(s)

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 2 November 2017
                : 2 February 2018
                : 23 February 2018
                Categories
                Article

                Life sciences
                myelin,oligodendrocyte,neuron,axon,myelination,cns,myelin mistargeting,zebrafish
                Life sciences
                myelin, oligodendrocyte, neuron, axon, myelination, cns, myelin mistargeting, zebrafish

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