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      Glial Cell-Axonal Growth Cone Interactions in Neurodevelopment and Regeneration

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          Abstract

          The developing nervous system is a complex yet organized system of neurons, glial support cells, and extracellular matrix that arranges into an elegant, highly structured network. The extracellular and intracellular events that guide axons to their target locations have been well characterized in many regions of the developing nervous system. However, despite extensive work, we have a poor understanding of how axonal growth cones interact with surrounding glial cells to regulate network assembly. Glia-to-growth cone communication is either direct through cellular contacts or indirect through modulation of the local microenvironment via the secretion of factors or signaling molecules. Microglia, oligodendrocytes, astrocytes, Schwann cells, neural progenitor cells, and olfactory ensheathing cells have all been demonstrated to directly impact axon growth and guidance. Expanding our understanding of how different glial cell types directly interact with growing axons throughout neurodevelopment will inform basic and clinical neuroscientists. For example, identifying the key cellular players beyond the axonal growth cone itself may provide translational clues to develop therapeutic interventions to modulate neuron growth during development or regeneration following injury. This review will provide an overview of the current knowledge about glial involvement in development of the nervous system, specifically focusing on how glia directly interact with growing and maturing axons to influence neuronal connectivity. This focus will be applied to the clinically-relevant field of regeneration following spinal cord injury, highlighting how a better understanding of the roles of glia in neurodevelopment can inform strategies to improve axon regeneration after injury.

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          The origin and development of glial cells in peripheral nerves.

          During the development of peripheral nerves, neural crest cells generate myelinating and non-myelinating glial cells in a process that parallels gliogenesis from the germinal layers of the CNS. Unlike central gliogenesis, neural crest development involves a protracted embryonic phase devoted to the generation of, first, the Schwann cell precursor and then the immature Schwann cell, a cell whose fate as a myelinating or non-myelinating cell has yet to be determined. Embryonic nerves therefore offer a particular opportunity to analyse the early steps of gliogenesis from transient multipotent stem cells, and to understand how this process is integrated with organogenesis of peripheral nerves.
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            Layer V cortical neurons require microglial support for survival during postnatal development.

            Neurons require trophic support during neural circuit formation; however, how the cellular milieu contributes to neuronal survival remains unclear. We found that layer V cortical neurons require support from microglia for survival during postnatal development. Specifically, we found that microglia accumulated close to the subcerebral and callosal projection axons in the postnatal brain. Inactivation of microglia by minocycline treatment or transient ablation of microglia in CD11b-DTR transgenic mice led to increased apoptosis, specifically in layer V subcerebral and callosal projection neurons. CX3CR1 in microglia was required for the survival of layer V neurons. Microglia consistently promoted the survival of cortical neurons in vitro. In addition, we identified microglia-derived IGF1 as a trophic factor that maintained neuronal survival. Our results highlight a neuron-glia interaction that is indispensable for network formation during a specific period in the developing brain.
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              Moving beyond the glial scar for spinal cord repair

              Traumatic spinal cord injury results in severe and irreversible loss of function. The injury triggers a complex cascade of inflammatory and pathological processes, culminating in formation of a scar. While traditionally referred to as a glial scar, the spinal injury scar in fact comprises multiple cellular and extracellular components. This multidimensional nature should be considered when aiming to understand the role of scarring in limiting tissue repair and recovery. In this Review we discuss recent advances in understanding the composition and phenotypic characteristics of the spinal injury scar, the oversimplification of defining the scar in binary terms as good or bad, and the development of therapeutic approaches to target scar components to enable improved functional outcome after spinal cord injury.
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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
                10 March 2020
                2020
                : 14
                : 203
                Affiliations
                [1] 1Department of Medicine, University of Wisconsin-Madison , Madison, WI, United States
                [2] 2Neuroscience Training Program, University of Wisconsin-Madison , Madison, WI, United States
                [3] 3Waisman Center, University of Wisconsin-Madison , Madison, WI, United States
                [4] 4Department of Neuroscience, University of Wisconsin-Madison , Madison, WI, United States
                [5] 5Geriatric Research Education Clinical Center, Veterans Affairs Medical Center , Madison, WI, United States
                Author notes

                Edited by: Benedikt Berninger, King’s College London, United Kingdom

                Reviewed by: Raúl E. Russo, Instituto de Investigaciones Biológicas Clemente Estable (IIBCE), Uruguay; Brian Key, University of Queensland, Australia

                *Correspondence: Luigi Puglielli, lp1@ 123456medicine.wisc.edu

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

                Article
                10.3389/fnins.2020.00203
                7076157
                32210757
                99a46e72-67aa-462b-ad5a-76f5f55de298
                Copyright © 2020 Rigby, Gomez and Puglielli.

                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
                : 20 January 2020
                : 24 February 2020
                Page count
                Figures: 3, Tables: 2, Equations: 0, References: 181, Pages: 19, Words: 0
                Funding
                Funded by: National Institutes of Health 10.13039/100000002
                Funded by: U.S. Department of Veterans Affairs 10.13039/100000738
                Categories
                Neuroscience
                Review

                Neurosciences
                glia,growth cone,axon,neurodevelopment,cell-cell interaction,spinal cord injury
                Neurosciences
                glia, growth cone, axon, neurodevelopment, cell-cell interaction, spinal cord injury

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