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      The Axon-Myelin Unit in Development and Degenerative Disease

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          Abstract

          Axons are electrically excitable, cable-like neuronal processes that relay information between neurons within the nervous system and between neurons and peripheral target tissues. In the central and peripheral nervous systems, most axons over a critical diameter are enwrapped by myelin, which reduces internodal membrane capacitance and facilitates rapid conduction of electrical impulses. The spirally wrapped myelin sheath, which is an evolutionary specialisation of vertebrates, is produced by oligodendrocytes and Schwann cells; in most mammals myelination occurs during postnatal development and after axons have established connection with their targets. Myelin covers the vast majority of the axonal surface, influencing the axon's physical shape, the localisation of molecules on its membrane and the composition of the extracellular fluid (in the periaxonal space) that immerses it. Moreover, myelinating cells play a fundamental role in axonal support, at least in part by providing metabolic substrates to the underlying axon to fuel its energy requirements. The unique architecture of the myelinated axon, which is crucial to its function as a conduit over long distances, renders it particularly susceptible to injury and confers specific survival and maintenance requirements. In this review we will describe the normal morphology, ultrastructure and function of myelinated axons, and discuss how these change following disease, injury or experimental perturbation, with a particular focus on the role the myelinating cell plays in shaping and supporting the axon.

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          Most cited references191

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          Myelination of the nervous system: mechanisms and functions.

          Myelination of axons in the nervous system of vertebrates enables fast, saltatory impulse propagation, one of the best-understood concepts in neurophysiology. However, it took a long while to recognize the mechanistic complexity both of myelination by oligodendrocytes and Schwann cells and of their cellular interactions. In this review, we highlight recent advances in our understanding of myelin biogenesis, its lifelong plasticity, and the reciprocal interactions of myelinating glia with the axons they ensheath. In the central nervous system, myelination is also stimulated by axonal activity and astrocytes, whereas myelin clearance involves microglia/macrophages. Once myelinated, the long-term integrity of axons depends on glial supply of metabolites and neurotrophic factors. The relevance of this axoglial symbiosis is illustrated in normal brain aging and human myelin diseases, which can be studied in corresponding mouse models. Thus, myelinating cells serve a key role in preserving the connectivity and functions of a healthy nervous system.
            • Record: found
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            • Article: not found

            Reversal of neurological defects in a mouse model of Rett syndrome.

            Rett syndrome is an autism spectrum disorder caused by mosaic expression of mutant copies of the X-linked MECP2 gene in neurons. However, neurons do not die, which suggests that this is not a neurodegenerative disorder. An important question for future therapeutic approaches to this and related disorders concerns phenotypic reversibility. Can viable but defective neurons be repaired, or is the damage done during development without normal MeCP2 irrevocable? Using a mouse model, we demonstrate robust phenotypic reversal, as activation of MeCP2 expression leads to striking loss of advanced neurological symptoms in both immature and mature adult animals.
              • Record: found
              • Abstract: found
              • Article: not found

              Myelination and support of axonal integrity by glia.

              The myelination of axons by glial cells was the last major step in the evolution of cells in the vertebrate nervous system, and white-matter tracts are key to the architecture of the mammalian brain. Cell biology and mouse genetics have provided insight into axon-glia signalling and the molecular architecture of the myelin sheath. Glial cells that myelinate axons were found to have a dual role by also supporting the long-term integrity of those axons. This function may be independent of myelin itself. Myelin abnormalities cause a number of neurological diseases, and may also contribute to complex neuropsychiatric disorders.

                Author and article information

                Contributors
                Journal
                Front Neurosci
                Front Neurosci
                Front. Neurosci.
                Frontiers in Neuroscience
                Frontiers Media S.A.
                1662-4548
                1662-453X
                11 July 2018
                2018
                : 12
                : 467
                Affiliations
                [1] 1Department of Neurogenetics, Max-Planck-Institute of Experimental Medicine , Göttingen, Germany
                [2] 2Department of Neuropathology, University Medical Center Leipzig , Leipzig, Germany
                [3] 3Institute of Infection, Immunity and Inflammation, College of Medical Veterinary and Life Sciences, University of Glasgow , Glasgow, United Kingdom
                Author notes

                Edited by: Robert W. Burgess, Jackson Laboratory, United States

                Reviewed by: John Svaren, University of Wisconsin-Madison, United States; Andrea Loreto, University of Cambridge, United Kingdom

                *Correspondence: Klaus-Armin Nave nave@ 123456em.mpg.de

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

                Article
                10.3389/fnins.2018.00467
                6050401
                30050403
                47689c81-5dfd-4104-9ef5-6f9a6e33a57c
                Copyright © 2018 Stassart, Möbius, Nave and Edgar.

                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
                : 27 February 2018
                : 19 June 2018
                Page count
                Figures: 5, Tables: 1, Equations: 0, References: 238, Pages: 22, Words: 18475
                Funding
                Funded by: Multiple Sclerosis Society 13039/501100000381
                Award ID: 038
                Funded by: Horizon 2020 10.13039/501100007601
                Award ID: 734584
                Funded by: European Research Council 10.13039/501100000781
                Award ID: MyeliNANO
                Categories
                Neuroscience
                Review

                Neurosciences
                oligodendrocyte,schwann cell,cytoskeleton,axonal transport,energy,neuroinflammation,morphology

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